Role of Transient Receptor Potential Vanilloid Channels in Gastrointestinal Physiology and Pathology

1. Introduction

The gastrointestinal tract (GIT) is indispensable for human well-being as it performs various physiological functions fundamental to overall health. Its efficiency is contingent on a diverse array of components, including gut microbiota, hormone-secreting cells, Gut-Associated Lymphoid Tissue (GALT), and an intricate network of ion channels [1]. Indeed, the GIT constitutes a complex network of diverse ion channels that facilitate the transport of various substances essential for its proper functioning. These channels play a vital role in maintaining the delicate balance of ions, nutrients, and other molecules needed for digestion, nutrient absorption, and overall gut health [2]. Accordingly, the regulation of such channels is finely tuned to respond to an array of stimuli, ranging from changes in the composition of ingested food to temperature, voltage, pressure, osmolarity and tension [3].

As part of the vast network of ion channels present in the human body, one notable family is the Transient Receptor Potential (TRP) channels. Prominently, these non-selective cation channels are involved in mediating various physiological processes. While their significant role in the GIT cannot be overlooked, TRP channels are also found in various other tissues and organs, including the nervous system, skin, bladder, lungs, and cardiovascular system [4,5,6]. TRP channels are involved in sensory perception of temperature, pain, taste, and touch. TRP channels are also pivotal for mediating the responses to chemical, mechanical, and osmotic changes in the environment [7]. Such multifaceted functionality is facilitated by their unique ability to allow transmembrane passage of various ions, including calcium, sodium, potassium, and magnesium [4]. These channels are classified into seven subfamilies based on sequence homology and functional properties, each holding distinct properties and characteristics. These include canonical (TRPC), vanilloid (TRPV), melastatin (TRPM), mucolipins (TRPML), no-mechano-potential (TRPN), ankyrin (TRPA), and polycystin (TRPP) [8].

TRPV channels are named after the first identified member TRPV1, that is sensitive to the vanillylamide capsaicin, the compound responsible for the hot and spicy sensation in chili peppers [9,10]. Such channels bear considerable importance due to widespread expression across the GIT. They play vital roles in the regulation of gut motility, secretion, pain perception, and responses to chemical and thermal stimuli. Among the TRPV subfamily, both non-selective cation channels, TRPV1-4, and selective cation channels, TRPV5-6, are identified to serve distinct yet interrelated functions [11].

Given their intricate involvement in normal body physiology, it comes as no surprise that disruptions in the function or regulation of TRPV channels are involved in numerous gastrointestinal (GI) abnormalities. Their influence on GI disorders has been associated with a broad spectrum of conditions, acting both as protective agents and contributors in disease development, including GI cancers and neuroendocrine tumors (NETs) [12]. Recognizing this, it becomes imperative to emphasize that acquiring a comprehensive understanding of the ramifications of TRPV channels’ malfunctions offers valuable insights into potential therapeutic methods for dealing with related pathologies.

Accordingly, in this comprehensive review, we will delve into the intricate roles and implications of TRPV channels in various GI diseases, aiming to illuminate their significance in pathological contexts and uncover potential avenues for future research and therapeutic interventions.

2. Methods

A comprehensive literature search was conducted on May 27, 2025, and updated on August 4, 2025, to identify studies exploring the role of TRPV channels in gastrointestinal physiology and pathology. Databases searched included PubMed, Scopus, Web of Science, Google Scholar, and Embase. The search strategy used the following string for PubMed and was adapted for other databases:

((TRPV Cation Channels [MeSH Terms]) OR (Transient Receptor Potential Channels [MeSH Terms]) OR (TRPV [Title/Abstract]) OR (Transient Receptor Potential Vanilloid [Title/Abstract])) AND ((Gastrointestinal Tract [MeSH Terms]) OR (Gut [Title/Abstract]))

Additional relevant articles were identified through forward and backward snowballing (citation tracking) of the included studies [13]. Inclusion criteria were peer-reviewed articles published in English from database inception to the search date. Studies were excluded if they were not focused on the GI tract, were not in English, or lacked sufficient scientific detail. Search results were screened by title and abstract for relevance. Included studies were categorized into four TRPV-related thematic areas: architecture, physiology, pathology, and pharmacology. Each thematic area was assigned to a pair of authors who collected and synthesized the evidence. Their synthesized summaries were then critically revised and approved by the senior author to ensure accuracy and coherence.

3. The General Structure of TRPV Channels

TRPV channels are characterized by their tetrameric arrangement, much like voltage-gated ion channels, and have transmembrane and cytoplasmic domains. Each TRPV channel has four monomers that assemble together in a ring-like structure (Figure 1). Each monomer consists of six transmembrane segments labelled S1 to S6 linked to each other through extracellular and intracellular loops [14]. The first four segments, S1 to S4, operate in a manner similar to voltage-sensing domains (VSDs) found in other ion channels, and are therefore collectively referred to as voltage-sensing-like domain (VSLD). This domain is connected to an inner pore region consisting of S5 and S6 bridged by the S4S5-linker. The precise location of this linker is of great importance in regulating channel gating, determining when the channel opens and closes [15]. Together with the S4S5-linker, S5 and S6 are positioned adjacent to other domains, encircling the inner pore to form the lower gate of the channel [11]. On the other hand, the formation of the upper gate is ascribed to the pore helix (PH), formed by a short loop and a helix, which plays an important role in determining the ion selectivity properties of TRPV channels, allowing certain cations in but not others [16].

Focusing on the cytoplasmic domain of TRPV channels, a distinctive structural arrangement is observed, characterized by a larger N-terminus and a smaller C-terminus (Figure 2). The N-terminus harbors two β-sheets found between a pre-S1 helix and six ankyrin repeats [4]. These repeats collectively form the ankyrin repeat domain (ARD) which stands out due to its interaction with the β-sheets of neighboring monomers, resulting in the formation of a skirt-like structure [17]. This structural motif serves as a platform for intricate engagements with regulatory proteins, thereby exerting a significant influence in modulating the channel’s activity [18]. The C-terminus, on the contrary, contains the TRP domain and is associated with one β-sheet.

TRPV channels are non-selective cation channels that permit the influx of calcium and other cations upon activation. Their activity can be modulated by G protein-coupled receptors (GPCR) signaling pathways through second messengers such as diacylglycerol (DAG), phospholipase C (PLC), or changes in intracellular calcium levels [19]. Activation of TRPV channels, whether by ligand binding or other stimuli, induces conformational changes that open the channel pore, allowing the entry of ions including sodium and calcium, depending on the channel’s permeability. TRPV stimulation also triggers intracellular signaling cascades, prominently involving PLC. This enzyme catalyzes the hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP₂) into inositol 1,4,5-trisphosphate (IP₃) and DAG. IP₃ promotes the release of calcium from intracellular stores in the smooth endoplasmic reticulum, producing downstream cellular effects, while DAG activates protein kinase C (PKC), a serine/threonine kinase, that phosphorylates target proteins and modulates their activity [20].

4. TRPV Channels in GI Physiology

The following section explores each of the TRPV channels individually, outlining their physiological roles, known activators, and involvement in gastrointestinal function. Table 1 summarizes key characteristics of these channels, including where they are expressed, activation mechanisms, and associated GIT-related effects.

4.1. TRPV1

TRPV1 channel is a polymodal sensor activated by a wide range of stimuli, including temperatures above 42°C, low pH, hyperosmolarity, capsaicin, 2-arachidonoylglycerol (2-AG) and endovanilloids such as anandamide [21,22]. Additionally, it is activated by endogenous lipids like oleoylethanolamide (OLDA), which binds to the receptor's vanilloid site to promote calcium influx and nociceptive signaling [23]. It is primarily present in the sensory neurons of the peripheral nervous system, dorsal root ganglia (DRG), and trigeminal ganglia, where it plays a pivotal role in sensing temperature and pain, mediating responses to noxious heat and chemical irritants [9]. Within the GIT, TRPV1 channel is located on the enteric neurons, contributing to visceral pain perception and the regulation of GI motility and secretion. This is attributed to the eventual release of neuropeptides such as substance P and calcitonin gene-related peptide (CGRP) upon the activation of TRPV1 channel [24]. Additionally, TRPV1 is implicated in modulating vagally-mediated contractions of the striated part of the esophagus, as well as regulating gastric acid secretion, gastric emptying, and visceral pain perception in response to inflammatory mediators [25]. Emerging evidence suggests that TRPV1 also plays a role in gastric mucosal defense mechanisms by promoting the release of mucus and bicarbonate, thus protecting the epithelial lining from acidic and mechanical damage [26]. Furthermore, TRPV1 activation has been linked to the modulation of immune responses within the stomach and small intestines of the GIT, influencing inflammatory pathways that can affect conditions such as gastritis and inflammatory bowel disease [27,28].

4.2. TRPV2

TRPV2 channel is activated by high temperatures, usually above 50-52°C, mechanical stimuli, and endogenous lipids such as 2-AG and lysophosphatidylcholine (LPC) [29,30,31]. It is also a target for pharmacological agents, most notably Cannabidiol (CBD), a natural compound from Cannabis sativa that acts as a potent and direct agonist of the channel [32]. This channel demonstrates widespread expression across various tissues, thereby contributing to diverse cellular processes, including immune responses, inflammation, and cellular homeostasis [33]. Indeed, its expression in the enteric immune cells including macrophages, dendritic cells, and T cells signifies its role in regulating inflammatory responses and enhancing mucosal immunity within the GIT [34]. Furthermore, in rodents, TRPV2 channel has also been identified in enteric neurons, where its stimulation influences downstream neurotransmitter release, thereby affecting GI movement and secretion. Specifically, TRPV2 was shown to mediate nitric oxide (NO) release. NO is a key inhibitory neurotransmitter which regulates intestinal motility by inducing smooth muscle relaxation. This was demonstrated through studies showing that TRPV2 activation, by mechanical or chemical stimuli such as probenecid and lysophospholipids, inhibited spontaneous intestinal contractions through enteric neurons [35,36].

4.3. TRPV3

TRPV3 channel is activated by innocuous temperatures exceeding 30–33°C, natural compounds like camphor, 2-aminoethoxydiphenyl borate (2-APB), and endogenous lipids such as 12-hydroxyeicosatetraenoic acid (12-HETE) [37]. It is also robustly activated by a variety of natural monoterpenes found in plants, including menthol, carvacrol, thymol, and carveol [38]. This channel is primarily expressed in epidermal keratinocytes where it plays a vital role in sensing warmth and maintaining skin barrier function [39,40,41]. Although TRPV3 channel has been extensively studied in the context of skin physiology, emerging research suggests its expression in the brain, particularly in regions associated with appetite regulation [42]. Additionally, TRPV3 is expressed in the GIT, particularly in the cecum and colon, where it plays a crucial role in ammonium (NH₄⁺) transport through its divalent-sensitive cation conductance [43]. Thus, TRPV3 contributes to nitrogen metabolism and gut homeostasis. It is localized predominantly to the apical membranes of epithelial cells, influencing epithelial permeability and maintaining barrier integrity by facilitating ion exchange under varying physiological conditions [44]. TRPV3 responds to changes in luminal ionic environments, modulating transepithelial ionic balance and supporting processes such as motility and secretion. Its frequent colocalization with TRPV4 suggests cooperative functions in osmoregulation and mechanosensation, while its presence in regions of high microbial activity highlights its potential role in host-microbe interactions and nutrient absorption [44,45].

4.4. TRPV4:

TRPV4 channel is widely expressed in multiple tissues and cell types, including endothelial cells, sensory neurons, urothelial cells, and chondrocytes [5,46,47,48,49]. Its activation is elicited in response to diverse stimuli, including mechanical stress, osmotic changes, moderate temperatures ranging from 25 to 35°C, and arachidonic acid metabolites. TRPV4’s activation enhances calcium signaling, influencing ion transport, epithelial barrier function, and sensory transduction pathways across the GI tract [50,51,52,53]. In the GIT milieu, it is distinguished by its involvement in regulating GI motility, fluid secretion across various exocrine glands, including salivary glands, where its activation is essential for regulating salivary flow. This regulation is mediated by the channel’s sensitivity to osmotic changes and mechanical stress, enabling it to facilitate water and ion movement across epithelial cells [54]. TRPV4 channel’s responsiveness to mechanical stimuli entitles it for the active participation in GI mechanosensation, influencing processes such as gastric emptying and intestinal transit [55]. In the esophagus, TRPV4 channel regulates calcium influx and ATP release in response to mechanical and chemical stimuli [56]. Similarly, in the stomach, TRPV4 is expressed at both mRNA and protein levels in mouse and rat gastric epithelial cells; upon activation by mechanical stretch or the selective agonist GSK1016790A -a TRPV-agonizing pharmacological tool developed by GlaxoSmithKline (GSK)- it induces calcium entry, generates TRPV4-like currents in the epithelial cells, and promotes ATP release [57]. These activities are crucial for maintaining epithelial integrity, sensory transduction, and protecting against mechanical damage from food passage. TRPV4 also contributes to esophageal mechanosensation, helping regulate peristalsis and coordinating the esophageal response to distension [55,58]. The channel’s activation in the stomach modulates calcium influx and ATP release, processes essential for maintaining gastric epithelial health and protecting against mechanical or chemical injury [57]. Additionally, TRPV4 plays a role in regulating gastric motility and pancreatic fluid secretion, impacting digestion and the maintenance of an optimal environment for enzymatic activity. Dysregulation of TRPV4 activity in the stomach has been associated with gastric dysfunction and potential involvement in inflammatory conditions [59].

4.5. TRPV5 and TRPV6

TRPV5 and TRPV6 channels are predominantly expressed in the GI epithelial cells and are crucial for maintaining calcium homeostasis. These channels are highly selective for calcium ions, distinguishing them from the previously mentioned TRPV channels [60]. Importantly, unlike other TRPV members, TRPV5 and TRPV6 have not been shown to be temperature-sensitive [61]. Their expression and activity are significantly upregulated by the active form of vitamin D, 1,25-dihydroxyvitamin D3 (1,25[OH]2D3), which is a major hormonal regulator of systemic calcium balance [62,63]. The activity of TRPV5 is tightly regulated by various factors, including the anti-aging hormone Klotho and sialidase, which modulate its expression and function at the cell surface [64]. Furthermore, the membrane phospholipid PIP₂ is a critical activator; for TRPV5, its direct binding is essential for channel opening, while for TRPV6, it enhances function by relieving auto-inhibition [65,66]. They are activated by extracellular calcium, enabling the influx of calcium ions across the apical membrane of epithelial cells of the small intestine, particularly in the duodenum and jejunum, where active calcium absorption occurs [60]. This mechanism is instrumental in maintaining systemic calcium balance and supporting various physiological functions, including neuromuscular excitability and bone health. Moreover, TRPV6 channel participates in the absorption of magnesium within the intestine and serves crucial functions in cellular signaling pathways, which in turn influence pivotal processes including cell proliferation, differentiation, and apoptosis, making TRPV6 channel increasingly conspicuous as a potential target for cancer therapy [67,68].

Table 1. A summary of the physiological roles of the different TRPV channels in the GIT.

Channel	Key Activators	Localization and Expression	Physiological Functions in the GI Tract
TRPV1	Activated by temperatures above 42°C, hyperosmolarity, low pH, capsaicin, and endovanilloids such as anandamide [21,22]. Moreover, It is activated by the endogenous lipid mediator oleoylethanolamide (OLDA) [38].	Primarily localized in sensory neurons of the peripheral nervous system, dorsal root ganglia, and trigeminal ganglia [9], as well as in enteric neurons within the gastrointestinal tract (GIT) [24].	TRPV1 senses temperature and pain, mediating responses to noxious heat and chemical irritants [9]. It contributes to visceral pain perception [25] and regulates GI motility and secretion [25]. It modulates vagally-mediated contractions of the striated part of the esophagus , regulates gastric acid secretion and gastric emptying [25], and is implicated in gastric mucosal defense by promoting mucus and bicarbonate release [27,28]. Additionally, it modulates immune responses in the stomach and small intestines [27,28].
TRPV2	Activated by high temperatures (above 50–52°C), mechanical stimuli, and endogenous lipids such as 2-arachidonoylglycerol (2-AG) and lysophosphatidylcholine (LPC) [29,30,31].	Exhibits widespread expression across various tissues [33], including enteric immune cells such as macrophages, dendritic cells, and T cells [34], and has been identified in enteric neurons in rodents [35,36].	TRPV2 contributes to diverse cellular processes, including immune responses and inflammation [33], and regulates inflammatory responses while enhancing mucosal immunity within the GIT [34]. Its stimulation in enteric neurons influences downstream neurotransmitter release [35,36] and mediates nitric oxide (NO) release, a key inhibitory neurotransmitter that regulates intestinal motility by inducing smooth muscle relaxation [35,36].
TRPV3	Activated by temperatures exceeding 30–33°C, natural compounds like camphor and 2-aminoethoxydiphenyl borate (2-APB), and endogenous lipids such as 12-hydroxyeicosatetraenoic acid (12-HETE) [37]. Additionally, Cannabidiol (CBD) potently agonises TRPV3 [32].	Primarily expressed in epidermal keratinocytes [39,40,41], with suggested expression in the brain [42]. In the GIT, it is expressed particularly in the cecum and colon [43], and is localized predominantly to the apical membranes of epithelial cells [44].	TRPV3 plays a vital role in sensing warmth and maintaining skin barrier function [39,40,41]. In the gut, it plays a crucial role in ammonium (NH₄⁺) transport through its divalent-sensitive cation conductance [43], contributing to nitrogen metabolism and gut homeostasis [43]. It influences epithelial permeability and maintains barrier integrity [44], modulates transepithelial ionic balance [44,45], and may have a potential role in host-microbe interactions and nutrient absorption [44,45].
TRPV4	Activated by mechanical stress, osmotic changes, moderate temperatures (25–35°C), arachidonic acid metabolites, and the selective pharmacological agonist GSK1016790A [50,51,52,53,57].	Widely expressed in multiple tissues and cell types [5,46,47,48,49], including endothelial cells, sensory neurons, urothelial cells, and chondrocytes [5,46,47,48,49]. It is present in the GIT milieu [54], and expressed in salivary glands, esophagus, and stomach [54,56,57]	TRPV4 is involved in regulating GI motility [54]and fluid secretion, which is essential for salivary flow [54]. It actively participates in GI mechanosensation, influencing gastric emptying and intestinal transit [55]. It regulates calcium influx and ATP release in the esophagus and stomach [56,57], is crucial for maintaining epithelial integrity and sensory transduction pathways [57], contributes to esophageal mechanosensation and regulation of peristalsis [55,58], and plays a role in regulating gastric motility and pancreatic fluid secretion [57,59].
TRPV5 & TRPV6	While TRPV5 is positively modulated by Klotho and sialidase [64], both channels are activated by extracellular calcium as well as vitamin D, 1,25-dihydroxyvitamin D3 (1,25[OH]2D3) [60,62,63] and the membrane phospholipid phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), which is essential for TRPV5 opening and enhances TRPV6 function by relieving auto-inhibition [65,66].	Predominantly expressed in GI epithelial cells [60], specifically on the apical membrane of epithelial cells in the small intestine, particularly in the duodenum and jejunum [60].	These channels are crucial for maintaining calcium homeostasis [60], being highly selective for calcium ions and enabling calcium influx [60]. They are instrumental in maintaining systemic calcium balance [67,68]. TRPV6 also participates in the absorption of magnesium within the intestine [67,68] and influences cell proliferation, differentiation, and apoptosis via cellular signaling pathways [67,68].

Table 1. A summary of the physiological roles of the different TRPV channels in the GIT.

Channel	Key Activators	Localization and Expression	Physiological Functions in the GI Tract
TRPV1	Activated by temperatures above 42°C, hyperosmolarity, low pH, capsaicin, and endovanilloids such as anandamide [21,22]. Moreover, It is activated by the endogenous lipid mediator oleoylethanolamide (OLDA) [38].	Primarily localized in sensory neurons of the peripheral nervous system, dorsal root ganglia, and trigeminal ganglia [9], as well as in enteric neurons within the gastrointestinal tract (GIT) [24].	TRPV1 senses temperature and pain, mediating responses to noxious heat and chemical irritants [9]. It contributes to visceral pain perception [25] and regulates GI motility and secretion [25]. It modulates vagally-mediated contractions of the striated part of the esophagus , regulates gastric acid secretion and gastric emptying [25], and is implicated in gastric mucosal defense by promoting mucus and bicarbonate release [27,28]. Additionally, it modulates immune responses in the stomach and small intestines [27,28].
TRPV2	Activated by high temperatures (above 50–52°C), mechanical stimuli, and endogenous lipids such as 2-arachidonoylglycerol (2-AG) and lysophosphatidylcholine (LPC) [29,30,31].	Exhibits widespread expression across various tissues [33], including enteric immune cells such as macrophages, dendritic cells, and T cells [34], and has been identified in enteric neurons in rodents [35,36].	TRPV2 contributes to diverse cellular processes, including immune responses and inflammation [33], and regulates inflammatory responses while enhancing mucosal immunity within the GIT [34]. Its stimulation in enteric neurons influences downstream neurotransmitter release [35,36] and mediates nitric oxide (NO) release, a key inhibitory neurotransmitter that regulates intestinal motility by inducing smooth muscle relaxation [35,36].
TRPV3	Activated by temperatures exceeding 30–33°C, natural compounds like camphor and 2-aminoethoxydiphenyl borate (2-APB), and endogenous lipids such as 12-hydroxyeicosatetraenoic acid (12-HETE) [37]. Additionally, Cannabidiol (CBD) potently agonises TRPV3 [32].	Primarily expressed in epidermal keratinocytes [39,40,41], with suggested expression in the brain [42]. In the GIT, it is expressed particularly in the cecum and colon [43], and is localized predominantly to the apical membranes of epithelial cells [44].	TRPV3 plays a vital role in sensing warmth and maintaining skin barrier function [39,40,41]. In the gut, it plays a crucial role in ammonium (NH₄⁺) transport through its divalent-sensitive cation conductance [43], contributing to nitrogen metabolism and gut homeostasis [43]. It influences epithelial permeability and maintains barrier integrity [44], modulates transepithelial ionic balance [44,45], and may have a potential role in host-microbe interactions and nutrient absorption [44,45].
TRPV4	Activated by mechanical stress, osmotic changes, moderate temperatures (25–35°C), arachidonic acid metabolites, and the selective pharmacological agonist GSK1016790A [50,51,52,53,57].	Widely expressed in multiple tissues and cell types [5,46,47,48,49], including endothelial cells, sensory neurons, urothelial cells, and chondrocytes [5,46,47,48,49]. It is present in the GIT milieu [54], and expressed in salivary glands, esophagus, and stomach [54,56,57]	TRPV4 is involved in regulating GI motility [54]and fluid secretion, which is essential for salivary flow [54]. It actively participates in GI mechanosensation, influencing gastric emptying and intestinal transit [55]. It regulates calcium influx and ATP release in the esophagus and stomach [56,57], is crucial for maintaining epithelial integrity and sensory transduction pathways [57], contributes to esophageal mechanosensation and regulation of peristalsis [55,58], and plays a role in regulating gastric motility and pancreatic fluid secretion [57,59].
TRPV5 & TRPV6	While TRPV5 is positively modulated by Klotho and sialidase [64], both channels are activated by extracellular calcium as well as vitamin D, 1,25-dihydroxyvitamin D3 (1,25[OH]2D3) [60,62,63] and the membrane phospholipid phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2), which is essential for TRPV5 opening and enhances TRPV6 function by relieving auto-inhibition [65,66].	Predominantly expressed in GI epithelial cells [60], specifically on the apical membrane of epithelial cells in the small intestine, particularly in the duodenum and jejunum [60].	These channels are crucial for maintaining calcium homeostasis [60], being highly selective for calcium ions and enabling calcium influx [60]. They are instrumental in maintaining systemic calcium balance [67,68]. TRPV6 also participates in the absorption of magnesium within the intestine [67,68] and influences cell proliferation, differentiation, and apoptosis via cellular signaling pathways [67,68].

5. Potential Role of TRPV Channels in the Pathophysiology of Different GIT Disorders:

TRPV channels have been implicated in a multitude of GI pathologies, spanning from pain and dysmotility to secretion abnormalities, inflammation, and ulcer formation. Their diverse roles in modulating sensory perception, cellular signaling, secretion, motility, and immune responses within the GIT underscore their potential role as therapeutic targets for developing novel interventions aimed at improving overall GI health. Targeting TRPV channels has been shown to alleviate GI symptoms, improve motility and secretion, reduce inflammation, and modulate ulcer formation and healing.

5.1. Mediation of Gut Pain

Gut pain is initiated primarily when noxious chemical, mechanical, or inflammatory stimuli activate sensory afferents innervating the intestinal wall. Excitable cells, such as DRG and intrinsic enteric neurons, transduce these stimuli into electrical signals, while non-excitable cells, including epithelial cells, enteroendocrine cells, and immune cells, contribute by releasing mediators such as ATP, histamine, serotonin [69,70,71]. TRPV channels, widespread in the GIT, influence various physiological and sensory functions as previously elucidated [72]. In particular, TRPV1 and TRPV4 are key players in GI nociception [73] (Figure 3). Henceforth, the following sections aim to leverage our understanding of their roles that could potentially guide therapeutic strategies for gut-related pain relief.

5.1.1. TRPV1 Channel and Its Contribution to Gut Pain

TRPV1 channel serves as a pivotal player in pain perception and the nociceptive response linked to gut disorders. The core of the relationship between gut inflammation and hyperalgesia lies in the regulation of TRPV1 channel. In this paradigm, this channel becomes sensitized and upregulated [72]. This was evident in tissue samples from individuals with inflammatory bowel disease (IBD) and rectal hypersensitivity, showing increased TRPV1 expression, correlating with elevated hypersensitivity levels [74]. Moreover, the increase in TRPV1 channel expression is not only limited to conditions marked by overt inflammation; functional gut diseases also demonstrate this surge [73]. For instance, individuals with irritable bowel syndrome (IBS) exhibit elevated TRPV1 levels in the sigmoid colon, correlating with the severity of pain [75]. A parallel narrative emerges in cases of non-active IBD, where continual abdominal pain is associated with an abundance of TRPV1-expressing mucosal nerves [76]. This is similarly seen in cases of fecal urgency, idiopathic rectal hypersensitivity [77], and non-erosive esophageal reflux disease [78]. Furthermore, individual grappling with functional dyspepsia [79] and diarrhea-dominant IBS [80] exhibit increased pain sensitivity when TRPV1 is activated with capsaicin. These findings suggest that the inhibition and antagonism of TRPV1 channel offer substantial potential as a therapeutic strategy for mitigating or completely alleviating pain in both inflammatory and functional gut disorders.

5.1.2. TRPV4 Channel and Its Contribution to Gut Pain

TRPV4 channel plays a crucial role in mediating mechanical hyperalgesia in various GI disorders. It has been demonstrated that activators of TRPV4 channel intensify the response of sensory neurons within the colon of mice as well as an increase in mechanosensitivity in mesenteric and serosal sensory nerves [81]. Conversely, in TRPV4-deficient mice, there is a significant reduction in mechanosensitivity in these sensory nerves, along with diminished behavioral responses to nociceptive distention of the colon [82]. Henceforth, the increased mechanical responses to colorectal distension suggest that the activation of TRPV4 channel contributes to a heightened responsiveness of the sensory nerves [83]. This link to hyperalgesia triggered by mechanical forces emphasizes the essential role of TRPV4 channel as a primary detector of mechanical stimuli in the context of nociception.

Moreover, TRPV4 channel plays a role in transmitting pain induced by inflammation, acting as secondary transducers for heightened sensitivity to mechanical stimuli. Sensitization of TRPV4-expressing sensory neurons is triggered by inflammatory mediators such as prostaglandin E2 (PGE2), which activates Proteinase-Activated Receptor 2 (PAR-2). In the context of inflammation, particularly in allergy-induced inflammation, PAR-2 serves as a crucial integrator of signaling cascades, contributing to an increased perception of pain in the presence of hypotonic, mildly hypertonic, or mechanical stimuli [84]. Notably, TRPV4 channel coexists with PAR-2 in rat DRG neurons. The administration of PAR-2 agonists elicits mechanically-induced hyperalgesia in mice through a TRPV4-dependent mechanism [85]. Additionally, PAR-2 agonism enhances TRPV4 channel-mediated sensory nerve responses in the colon [81], where even sub-nociceptive doses of PAR-2 agonists sensitize colonic sensory nerve fibers to TRPV4 agonists [83]. Further studies demonstrate that activating PAR-2 through cathepsin S [86] or elastase [87] leads to TRPV4 activation, sensitizing nociceptors and enhancing sensitivity to mechanical stimuli during inflammation. Moreover, substances like serotonin and histamine can influence TRPV4 expression in murine colonic DRG neurons, intensifying mechanically-induced hyperalgesia due to TRPV4 agonism [88]. Furthermore, TRPV4 regulates pain signaling indirectly through ATP release. TRPV4 activation triggers calcium influx, which promotes ATP release from gastric epithelial cells via vesicular nucleotide transporter (VNUT). This ATP then acts on purinergic receptors on sensory neurons, amplifying nociceptive signaling and contributing to visceral hypersensitivity and inflammatory pain. Thus, the inhibition of TRPV4 or VNUT significantly reduces ATP release and mucosal inflammation [56]. Considering all this information, it is of no doubt that TRPV4 plays a significant role in the pathophysiology of inflammation, hyperalgesia, and pain. Therefore, it emerges as a promising and innovative therapeutic target for individuals experiencing gut pain.

5.2. Facilitation of Gut Motility and Regulation of Secretions

TRPV channels, notably TRPV1, TRPV2 and TRPV4, regulate gut motility (Figure 4) and secretions (Holzer, 2011b). Therefore, understanding their roles offers therapeutic potential for these channels to be targeted in the context of managing gut conditions related to motility and fluid secretion.

5.2.1. Role of TRPV1 Channel in the Motor Activity and Secretory Processes of the Gut

TRPV1 channel plays a crucial role in regulating gut motor activity (Figure 4 Panel A). When activated by stimuli such as capsaicin, this channel initiates the release of signaling molecules, influencing various gut components like esophageal striated muscles, smooth muscles, nervous system, and epithelial cells. This modulation, in turn, affects secretion and motility processes [89]. In terms of motility, TRPV1 activation results in the release of motor stimulants like tachykinins and ATP, or inhibitors such as vasoactive intestinal peptide (VIP), CGRP, and NO [25,90,91]. Moreover, in the mouse esophagus, capsaicin has been demonstrated to produce a significant inhibitory effect on vagal contractions in esophageal preparations with an intact mucosa, while no such effect is observed in preparations lacking mucosa. The TRPV1 channels have been identified as the key mediators of this inhibitory action of capsaicin on vagally-induced striated muscle contractions, primarily through mucosal primary afferents. These afferents, located within the mucosa and containing TRPV1-positive fibers, subsequently activate an inhibitory local reflex arc [90]. Indeed, it was demonstrated that the relaxing effect of capsaicin on the intestinal circular muscles of the distal colon, achieved by stimulating NO release, is markedly diminished in mice lacking the TRPV1 channel in comparison to their wildtype controls [92]. Under pathological conditions, the TRPV1 channel demonstrates critical importance in the modulation of GI motility, with its activation on afferent nerve fibers resulting in the initiation of sympathetic reflex pathways. This mechanistic response has been documented in clinical scenarios such as peritoneal irritation and laparotomy-induced impairment of GI transit [93]. This notion is further supported by observations indicating that TRPV1 blockers can alleviate experimental colitis-associated gastroparesis [94]. Additionally, TRPV1 channel plays a regulatory role in secretory processes throughout the alimentary canal, influencing both neurons and epithelial cells. This includes their involvement in saliva secretion, esophageal platelet-activating factor production, release of somatostatin and gastrin, and stimulation of prosecretory effects in the colon [95,96,97,98]. Collectively, these examples highlight TRPV1 channel essential role in digestive system motility and secretory processes.

5.2.2. Role of TRPV2 Channel in Motor Activity of the Gut

TRPV2 channel plays a vital role in gut motility, influencing both intestinal relaxation and peristaltic movement to enhance gut transit speed. These motile changes are attributed to TRPV2-mediated release of NO from the inhibitory motor neurons, potentially involving intrinsic sensory neurons as well (Figure 4 Panel B). Supporting this, TRPV2 activation in isolated intestinal tissue inhibited spontaneous circular muscle contractions in a manner dependent on NO and neuronal activity, and these responses were blocked by the TRPV2 antagonist tranilast [36]. This underscores the crucial involvement of TRPV2 channel activation in inducing intestinal relaxation, peristaltic movements, and enhanced transit speed via NO synthesis. Taken together, this growing body of evidence firmly establishes the essential role of TRPV2 in modulating gastrointestinal motility through NO-dependent regulatory pathways, positioning TRPV2 channels as promising therapeutic targets whose activation may offer novel solutions for managing GI motility disorders.

5.2.3. Role of TRPV4 Channel in Motor Activity and Secretory Processes of the Gut

TRPV4 channel plays a pivotal role in the secretory and mechanical functions of the gut, with their influence evident in various physiological processes (Figure 4 Panel C). In the hepatobiliary secretory system, both rat intrahepatic bile duct units and murine cholangiocytes exhibit heightened intracellular calcium levels under hypotonic conditions, a response that is magnified by TRPV4 agonists and attenuated with reduced TRPV4 expression [99]. Furthermore, the activation of TRPV4 in cholangiocytes induces bicarbonate secretion essential for bile synthesis. This is underscored by TRPV4 agonists enhancing bile flow and luminal secretion in rats, an effect counteracted by TRPV4 blockade [99]. Additionally, observations in a rat model of polycystic kidney disease reveal a correlation between cholangiocyte hyperproliferation and excessive, mislocalized TRPV4 expression. TRPV4 agonists effectively mitigate this proliferation and cyst development [100].

Moreover, the importance of TRPV4 channel in gut motility is closely tied to its interaction with intestinal muscularis macrophages (MMs). These TRPV4-expressing MMs establish connections with smooth muscle cells (SMCs) independent of neuronal input. Essentially, MMs release PGE2, initiating contractions in the colon that occur outside the influence of the enteric nervous system. Accordingly, under conditions of excessive gut motility, the removal or inhibition of TRPV4 from intestinal MMs results in diminished intestinal motility [101]. These findings open potential avenues for therapeutic interventions targeting TRPV4, particularly in the context of gut disorders associated with hypermotility.

5.3. Role of TRPV Channels in Gut Inflammation

TRPV channels, especially TRPV1, TRPV2, TRPV4, and TRPV6, play crucial roles in modulating gut inflammation, suggesting innovative therapeutic possibilities for various gut inflammatory disorders. Consequently, this section explores these inflammatory mechanisms governed by TRPV channels.

5.3.1. Role of TRPV1 Channel in Gut Inflammation

The activation of TRPV1 channel has been closely implicated in heightened inflammation observed in conditions such as pancreatitis, colitis, and ileitis [73]. The impact extends to esophageal health, where capsaicin and acid activation of TRPV1 have been linked to the development of esophagitis [96]. Notably, ethanol-induced damage to the stomach mucosa in murine models is attributed to TRPV1-mediated release of neuronal substance P [102]. In this context, substance P can modulate various physiological processes (Figure 5), including inflammation and pain perception, suggesting that its release in the stomach mucosa may be part of the response to ethanol exposure, potentially exacerbating the damage to the stomach lining. This is supported by an experiment conducted on mice with colitis, demonstrating that TRPV1 antagonism or genetic knockout contributes to the mitigation of inflammation, offering a promising avenue for therapeutic intervention [73]. The influence of TRPV1 is not confined to the gut alone, as it is implicated in pancreatic inflammation associated with types I and II diabetes, and obesity. Furthermore, TRPV1 exerts its impact on CD4+ T cells, influencing their activation and proinflammatory characteristics. Modulation of TRPV1 leads to reduced IL-2 production, coupled with elevated levels of IL-17 and IFN-γ production, all of which are pro-inflammatory mediators [103]. Consequently, the inhibition of TRPV1 emerges as a prospective and strategic therapeutic approach for mitigating inflammation within the GIT, particularly those of autoimmune nature.

5.3.2. Role of TRPV2 Channel in Gut Inflammation

In the gut, the expression of TRPV2 channel extends to the enteric neurons, SMCs, and immune cells, suggesting a possible role in modulating inflammation [104]. The role of TRPV2 in sensory neurons remains somewhat ambiguous; however, it was recently proven that there is an increase in TRPV2 expression in the dorsal root ganglia, needed for the transmission of sensory information. This implies a potential involvement in sensitization during inflammation, particularly in transmitting pain in response to noxious temperatures [105]. Moreover, in a study involving mice with colitis, it was found that mice lacking TRPV2 displayed a milder form of colitis compared to their wild-type counterparts. This observation could be attributed to a potential decrease in macrophage recruitment, pointing to the involvement of TRPV2 in the onset of colitis. Despite these findings, the precise mechanisms driving this effect remain to be fully understood [106].

5.3.3. Role of TRPV4 Channel in Gut Inflammation

Recent investigations spotlight the proinflammatory role of TRPV4 within the colonic mucosa. Specifically, the activation of TRPV4 by the agonist 4-α-phorbol 12, 13-di-decanoate (4αPDD) instigates an elevation in intracellular calcium levels, prompting the release of chemokines from intestinal epithelial cells. This agonist further increases paracellular permeability, leading to colitis when applied to murine colons [107]. Moreover, augmented TRPV4 expression manifests in mice with dextran sulfate sodium (DSS)-induced colitis and in the blood vessels of actively inflamed colonic tissues, as compared to their healthy controls [82]. There is also considerable promise in the observation that patients with IBD exhibited infiltration of TRPV4-positive and CD45-positive white blood cells in their colonic mucosa [107]. This indicates a potential involvement of TRPV4 channel in recruiting or activating immune cells, thereby contributing to the inflammatory processes observed in IBD. In both mouse and human colon, TRPV4 localizes to epithelial cells and certain unidentified cells within the submucosal and muscular layers. TRPV4 agonists can increase intracellular calcium concentrations and promote chemokine release in human colon cancer cell lines and induce colitis in mice [56]. Having said this, numerous research initiatives focusing on TRPV4 channel blockers have been initiated to explore the therapeutic potential of targeting TRPV4 in the context of gut inflammation [108].

5.3.4. Role of TRPV6 Channel in Gut Inflammation

Although not extensively explored, TRPV6 channel has emerged as a significant player in alcohol-induced gut inflammation and barrier dysfunction. Experiments involving Caco-2 cells, a line of colorectal adenocarcinoma cells, and mice intestinal organoids demonstrate that inhibiting TRPV6 mitigates the effects of ethanol and acetaldehyde, including calcium influx and barrier dysfunction [109]. Remarkably, mice lacking TRPV6 display resistance to alcohol-induced intestinal issues, underscoring the critical role of TRPV6 in this context. These findings emphasize the potential of targeting TRPV6 as prospective treatments for inflammatory gut disorders triggered by alcohol.

5.4. Role of TRPV Channels in Ulcer Formation and Healing

Ulcer formation and healing are dynamic and complex processes that involve the interplay of multiple cellular signaling pathways. These pathways are crucial for responding to injury, inflammation, and tissue repair. Emerging evidence underscores the significant involvement of TRPV channels in both the formation and healing of ulcers in the GIT. By influencing epithelial cell proliferation, migration, and mucosal repair mechanisms, these channels present promising therapeutic targets for improving recovery from ulcers and reducing their recurrence.

5.4.1. TRPV Channels and Ulcer Formation

Ulcers typically result from an imbalance between protective factors, such as the mucosal barrier and blood flow, and damaging factors, such as gastric acid, mechanical injury, and inflammation. In this context, TRPV channels, particularly TRPV1, TRPV2, and TRPV4, play critical roles in sensing noxious stimuli and triggering inflammatory responses that contribute to ulcer formation.

TRPV1 responds to gastric acid and mechanical damage in sensory neurons and epithelial cells in the GIT. It contributes to the protection of the GIT by enhancing mucosal blood flow and strengthening the epithelial barrier through the release of substance P and CGRP [96]. However, sustained or excessive TRPV1 activation can exacerbate inflammation and sensitivity, contributing to mucosal injury. This occurs through mechanisms including enhanced vasodilation and increased vascular permeability, resulting in the recruitment of immune cells to the affected area [110,111]. Additionally, the neuropeptides released stimulate pro-inflammatory cytokines, such as IL-1β and TNF-α, further amplifying inflammation and worsening mucosal damage [112]. This dysregulation is particularly evident in conditions of chronic stress such as Helicobacter pylori infection, acid reflux, and peptic ulcers, where heightened inflammatory responses exacerbate mucosal damage.

TRPV2 plays a multifaceted role in the GIT, extending beyond inflammatory pathways to include responses to mechanical stretch and thermal stimuli. This makes it a key player in ulcer formation, particularly under conditions of acid-induced injury or physical stress. TRPV2 channels are expressed in various GIT cell types, including epithelial cells, where their activation promotes the release of pro-inflammatory mediators and enhances cellular responses to mechanical stress [113]. By facilitating calcium influx, TRPV2 activates downstream signaling cascades involved in inflammation, contributing to tissue damage and disruption of mucosal integrity [114]. Although TRPV2 has not been as extensively studied as TRPV1, its capacity to sense mechanical stress and regulate inflammatory processes underscores its potential role in the early phases of ulcer pathogenesis.

TRPV4 has been implicated in the response to both mechanical stress and inflammatory mediators, playing a critical role in regulating inflammation in ulcerative conditions. Its activation stimulates PGE2 release from macrophages, thereby increasing mucosal permeability and contributing to tissue damage [101]. In esophageal epithelial cells, TRPV4 further exacerbates inflammation by enhancing calcium influx, which triggers the release of IL-1β and TNF-α, leading to greater tissue injury [115]. This mechanism is particularly relevant in conditions like gastroesophageal reflux disease (GERD) and peptic ulcers. Conversely, the inhibition of TRPV4 has been shown to attenuate inflammation, protect against mucosal injury and promote healing, highlighting its potential as a therapeutic target for ulcer-related disorders [55].

5.4.2. Role of TRPV Channels in Ulcer Healing

TRPV channels play multifaceted roles in wound healing within the GIT by modulating inflammation, cellular migration, and tissue regeneration. Among these, TRPV4 plays a dual and complex role in epithelial repair processes. Its activation in epithelial cells enhances intracellular calcium signaling, driving cytoskeletal reorganization and promoting cell migration across wounded areas [116]. TRPV4 activation in esophageal keratinocytes stimulates both proliferation and migration by upregulating key proteins involved in cell adhesion and movement, such as E-cadherin and integrins [117]. Additionally, calcium influx through TRPV4 channels supports the activation of crucial signaling pathways, including extracellular signal–regulated kinases 1 and 2 (ERK1/2) and phosphoinositide 3-kinase/protein kinase B (Akt) (PI3K/Akt), which are essential for cell survival and proliferation [116]. Paradoxically, TRPV4 can also act as a negative regulator of wound healing. Murine models have demonstrated that its deletion in esophageal keratinocytes significantly accelerates tissue repair by enhancing proliferation and speeding migration to the wound site [59]. This inhibitory role aligns with findings suggesting that TRPV4 modulates responses to mechanical stress and regulates tissue regeneration, potentially limiting effective epithelial repair [118].

Conversely, TRPV3 promotes epithelial repair by facilitating calcium influx and activating signaling pathways involved in cytokine release, cell proliferation, and migration. Expressed in both skin and GI tissues, TRPV3 activation enhances keratinocyte migration and accelerates wound closure, suggesting a similar role in GIT ulcer healing by promoting mucosal regeneration [119,120]. Similarly, TRPV2 supports wound healing by promoting keratinocyte migration, as demonstrated in skin models, indicating analogous function in GI ulcer repair [121]. However, its role in inflammatory processes suggests that excessive activation may prolong inflammation and impede healing, emphasizing the need for precise modulation.

Additionally, TRPV1 contributes to ulcer healing by promoting angiogenesis. Its activation on endothelial cells triggers the release of vasodilatory factors like CGRP and NO, enhancing blood flow to damaged tissues [122,123]. This vascularization is essential for delivering nutrients and immune cells necessary for effective repair, underscoring the therapeutic potential of targeting TRPV channels to optimize both inflammation and tissue regeneration.

5.4.3. Implications for Therapeutic Targeting of TRPV Channels in Ulcerative Diseases

The involvement of TRPV channels in both inflammation and ulcer healing positions them as promising targets for therapeutic intervention in ulcerative diseases. These channels contribute to the initiation of inflammatory processes that can worsen ulcer formation, while also playing key roles in epithelial regeneration and tissue repair. Targeting these pathways offers the potential to both prevent ulcer development and promote faster healing, making them valuable in managing conditions such as peptic ulcers, inflammatory bowel disease, and GERD.

TRPV1 antagonists have shown promise in reducing ulcer formation in animal models, with compounds that block TRPV1 reducing acid-induced injury and inflammatory responses [124]. Similarly, TRPV4 inhibitors also show promise for promoting ulcer healing, as studies on TRPV4 knockout mice demonstrated accelerated wound repair. Blocking TRPV4 activity may facilitate faster recovery of epithelial lesions, particularly in chronic ulcers where persistent inflammation frequently hinders the healing process [59]. Additionally, TRPV3 modulators could be useful in promoting ulcer healing by enhancing cell migration and proliferation, essential steps in mucosal repair. However, the challenge lies in balancing the activation of TRPV3, as its excessive activation could lead to uncontrolled proliferation or sustained inflammation. As such, the therapeutic application of TRPV3-targeting drugs would require a nuanced approach to prevent adverse effects while promoting healing. Lastly, the therapeutic targeting of TRPV2 remains an area for further exploration, especially in the context of mechanotransduction and wound healing. As TRPV2 is involved in both inflammation and cell migration, its modulation could offer benefits in managing both the inflammatory and repair phases of ulcerative diseases.

6. Role of TRPV Channels in GIT Tumors

TRPV channels play a pronounced role in digestive system tumors, of which, oral, esophageal, gastric, intestinal and colorectal tumors are studied [125]. These channels are implicated in the uncontrolled proliferation, increased invasion, migration, and immortality of such tumors [126]. The contribution of TRPV channels to cancer progression is primarily mediated through the dysregulation of intracellular Ca²⁺ levels, affecting cellular processes, including cell cycle progression and apoptosis. Alterations in TRPV channel activity in these malignancies are typically attributed to changes in TRPV mRNA and protein expression levels, whether increased or decreased, rather than mutations in TRP genes [127].

6.1. Oral Cavity Cancer

TRPV1 expression is notably heightened in both pre-malignant leukoplakia and tongue squamous cell carcinoma (SCC) [128]. Interestingly, while capsaicin demonstrates cytotoxic effects on oral SCC cells, this mechanism operates independently of TRPV1's typical Ca²⁺ conductivity pathway, as evidenced by the absence of intracellular Ca²⁺ elevation upon stimulation [129]. Instead, capsaicin-induced cytotoxicity has been associated with the generation of reactive oxygen species (ROS), mitochondrial dysfunction, and the activation of apoptotic signaling pathways, leading to cell death [130]. A study conducted in 2016 reported that patients with a history of smoking and alcohol consumption exhibited increased expression levels of TRPV1-4 mRNA. Moreover, elevated protein levels of TRPV1-4 have been observed in various regions of the oral cavity affected by SCC, including the tongue, gingiva, oral floor, and buccal mucosa, compared to normal tissue [131]. Among these, TRPV1 and TRPV3 are expressed at higher levels than TRPV2 and TRPV4. Activation of TRPV1 by its agonists, such as capsaicin, can induce cancer cell apoptosis via the generation of ROS. Conversely, TRPV1 activation may also stimulate cancer cell migration and invasiveness in certain contexts [131]. For instance, in hepatoblastoma, TRPV1 activation induced by hepatocyte growth factor (HGF) leads to an influx of Ca²⁺ into hepatoblastoma cells following capsaicin treatment, which enhances cell migration [132]. Similarly, TRPV4 in SCC has been implicated in promoting cancer cell proliferation and migration through activation of the calcium/calmodulin-dependent protein kinase II (CaMKII)-Akt signaling pathway [133].

6.2. Esophageal Cancer

Dysregulation of TRPV1, TRPV2, and TRPV4 has been observed in esophageal squamous cell carcinoma (ESCC), with these channels being overexpressed at both mRNA and protein levels compared to normal esophageal tissues. Hyperactive TRPV1 and TRPV4 have been shown to promote ESCC cell proliferation and migration [134]. Specifically, TRPV1 activation by capsaicin or heat exposure significantly increased both proliferation and migration, while these effects were effectively suppressed by the TRPV1 antagonist AMG9810, highlighting its therapeutic potential. Similar inhibitory effects have also been observed with other TRPV1 antagonists such as BCTC, which reduces capsaicin-induced responses and suppresses TRPV1-mediated cell signaling [135], and SB705498, a compound that potently blocks TRPV1 activation by capsaicin, heat, and protons, showing promise in both preclinical and clinical settings [136,137]. Moreover, TRPV4 activation enhanced cell migration but had no significant effect on proliferation; this pro-migratory effect was suppressed by the inhibitor ruthenium red [134]. In contrast, TRPV2 overexpression correlates with poor prognosis and increased tumor aggression [138,139]. Inhibiting TRPV2 in ESCC cells reduces proliferation, migration, and invasion, emphasizing its pivotal role in cancer progression [140,141].

6.3. Gastric Cancer

TRPV1 expression is markedly downregulated in primary gastric cancer (GC) tissues compared to adjacent normal tissues. This downregulation is correlated with larger tumor size, higher histological grade, advanced clinical stage, and poor survival in GC patients. TRPV1 inhibits GC development through the or calcium/calmodulin-dependent protein kinase kinase β/AMP-activated protein kinase (CaMKKβ/AMPK) pathway, highlighting its upregulation as a promising target for GC prevention and treatment [142]. Furthermore, elevated TRPV2 expression in GC patients has been identified as a prognostic biomarker and possible therapeutic target [143]. Additionally, research has shown that the calcium-sensing receptor (CaSR) and TRPV4 channel are co-expressed in GC cells; CaSR activation induces TRPV4-mediated Ca²⁺ entry, which promotes GC cell proliferation, migration, and invasion [144].

6.4. Intestinal Adenoma

While TRPV channels are involved in many malignant tumors, their role in benign tumors remains obscure. A study published in 2014 highlighted that TRPV1 deficiency promotes the formation of intestinal adenomas by impairing the regulatory interaction between TRPV1 and protein tyrosine phosphatase 1B. Under normal conditions, TRPV1 activation enhances this enzyme’s ability to suppress epidermal growth factor receptor (EGFR) signaling through the activation of Ca²⁺/calpain, thereby controlling epithelial cell proliferation in the intestinal lining. However, in the absence of TRPV1, this regulatory pathway is disrupted, leading to unchecked EGFR activation, excessive cell proliferation, and the development of adenomas [145]. Of the oncogenic pathways associated with TRPV1-EGFR signaling, signal transducer and activator of transcription 3 (STAT3), ERK1/2, and PI3K stand out. Without appropriate EGFR phosphorylation, oncogenesis is a likely destiny to many epithelial cells [145,146]. Beyond its role in adenoma formation, aberrant EGFR signaling is a well-established driver of tumor progression, contributing to increased proliferation, survival, and resistance to apoptosis in various cancers [147]. Similarly, VEGF promotes angiogenesis, which is critical for tumor growth and metastasis by ensuring adequate blood supply to the expanding tumor mass [148,149]. TRPV1’s role goes beyond intracellular signaling; these channels promote immune regulation by promoting the release of VIP and pituitary adenylate cyclase-activating peptide (PACAP), two important modularity cytokines. TRPV1 knockout mice showed enhanced release of IL-6 and IL-11, on top of the increased activity of the protumorigenic STAT3 and NF-κB signaling pathways [146]. Through our literature review, we witnessed that other TRPV channels have not been exclusively explored in the pathophysiology of intestinal adenoma, highlighting a significant gap in this area.

6.5. Colorectal Cancer

TRPV1 acts as a tumor suppressor in colorectal cancer (CRC), showing lower expression levels in CRC tissues compared to non-cancerous colorectal tissues. Activation of TRPV1 by capsaicin inhibits CRC growth and induces apoptosis via the p53 pathway [150]. Conversely, TRPV4 is upregulated in colon cancer, correlating with poorer prognosis. Its inhibition induces apoptosis and autophagy in colon cancer cells through phosphatase and tensin homolog deleted on chromosome 10 (PTEN) pathway activation. In addition, TRPV6 is overexpressed in CRC, correlating with early-stage cancer and increased invasiveness. Inhibition of TRPV6 expression suppresses proliferation and induces apoptosis in CRC cells [150].

6.6. Neuroendocrine Tumors

NETs represent a diverse group of neoplasms with clinical behavior ranging from benign and low-grade malignant to high-grade malignant forms [151]. Within this spectrum, TRP channels have been shown to play functionally relevant roles, including in insulinomas [152]. The role of TRPV channels is most clearly defined in pancreatic neuroendocrine tumors (PanNETs), where both TRPV1 and TRPV6 have distinct and significant functions. In human PanNET cell lines like BON-1 and QGP-1, TRPV1 activation by agonists such as capsaicin induces a robust calcium influx that directly stimulates the exocytosis of secretory granules, thereby increasing the release of hormones and neuroendocrine markers like chromogranin A. This effect is specifically blocked by TRPV1 antagonists like capsazepine [153]. Furthermore, TRPV1 transcripts and protein are detected in BON and CNDT2.5 carcinoid/NET lines, suggesting the existence of additional Ca²⁺-coupled growth pathways [154]. Pharmacologically, high-dose capsaicin exerts cytotoxic effects on PanNET cells by inducing mitochondrial dysfunction, loss of membrane potential, and caspase-3 activation leading to apoptosis, although these effects are only partially dependent on TRPV1 itself [155]. In contrast to this secretory role, TRPV6 drives tumor proliferation by maintaining elevated pro-growth calcium signals. Functional studies show that knocking down TRPV6 in BON-1 cells inhibits proliferation and reduces activity of the calcium-dependent transcription factor nuclear factor of activated T-cells (NFAT), confirming its role as a key oncogenic channel in PanNETs [154].

Similarly, the functions of TRPV channels in gastrointestinal carcinoid tumors (e.g., midgut NETs) represent a significant knowledge gap, with no direct studies available. By analogy to the serotonin-secreting BON-1 cell line, it is hypothesized that TRPV1 activation could potentially provoke serotonin release from enterochromaffin-derived carcinoid cells, potentially exacerbating carcinoid syndrome symptoms like flushing and diarrhea [153,156]. Notably, another channel, TRPA1, is highly expressed in enterochromaffin-like QGP-1 cells, where agonists such as allyl-isothiocyanate and cinnamaldehyde induce Ca²⁺ influx and robust serotonin release; this effect is blocked both by TRPA1 antagonists and siRNA, blocking channel function and knocking down the channel’s expression, respectively [157]. This mechanism is physiologically relevant as native enterochromaffin cells in human and rodent guts also use TRPA1 to trigger 5-HT secretion, reinforcing its role as a chemosensory channel [158]. A TRPV1 or TRPA1 antagonist could therefore theoretically help stabilize hormone release. Furthermore, given that TRPV6 is often upregulated in secretory cancers, a pro-proliferative role analogous to its function in PanNETs is possible, but this has not been investigated.

7. Potential Challenges with Targeting TRPVs for Therapy

The approach of addressing TRPV channels for therapeutic purposes seems to represent a noteworthy advancement in managing disorders within the GIT. However, several obstacles exist that impede the swift realization of its clinical implementation.

By now, it must be appreciated that TRPV channels are active across multiple body systems. This unquestionably needs to be considered when contemplating the feasibility of targeting these channels for therapeutic purposes. An illustrative instance involves the presence of TRPV4 channel not only within the GIT, but also within blood vessels and the heart, where it contributes to the regulation of vascular tone and blood pressure [159,160]. Consequently, if a therapeutic strategy is designed to antagonize TRPV4 channel in the GIT, there is a potential for this antagonism to also impact TRPV4 channel in cardiovascular tissues. As a result, unintended outcomes could arise, including alterations in blood vessel tone, blood pressure regulation, and other functional dysregulations. This could ultimately lead to the development of conditions like hypertension and arrhythmias [159]. This situation highlights the imperative for meticulous delivery methods as well as precision in the development of therapies targeting TRPV channels in an organ-specific approach.

Not only are TRPV channels involved in interconnected signaling pathways, but they also exhibit a polymodal activation characteristic. For instance, TRPV1 exhibits sensitivity to a range of stimuli including capsaicin, extracellular pH, and heat. This responsiveness, in turn, is intricately influenced by the presence and intensity of other stimuli, necessitating meticulous control and consideration of the existing microenvironment [161]. This nuanced interplay underscores the heightened risk and intricate nature of antagonizing TRPV channels; blocking one stimulus can lead to altered channel’s responses to other stimuli, thereby yielding unintended adverse outcomes – a challenge for pharmaceutical companies to tackle. Moreover, given the complexity of TRPV channels’ involvement, any modification to their engagement with the numerous signaling pathways they participate in carries the potential for disruption. To illustrate, TRPV4 channel plays a pivotal role in gut function by perceiving mechanical forces and osmotic pressure changes. When the gut experiences mechanical stretching due to factors like food movement or intestinal wall expansion, TRPV4 channel is activated. This activation prompts the entry of calcium ions into cells, initiating intracellular signaling pathways that influence smooth muscle contractions, mucosal secretion, and overall gut motility [73]. Conversely, the activation of TRPV4 channel is also linked to the regulation of epithelial barrier integrity, which is critical for maintaining the selective permeability of the intestinal lining [162]. Navigating these complexities presents a challenge when it comes to modulating or targeting TRPV channels. Any such interventions must account for the multifaceted roles within the gut and the potential ramifications for various signaling pathways.

The need for extensive research and efforts to develop agents targeting TRPV channels influenced by gene polymorphism might hinder the creation of successful targeted treatments. For instance, the human TRPV1 gene has been documented to possess six non-synonymous polymorphisms, leading to variations in responses to agonists like capsaicin and anandamide [163]. Some of these variations might heighten sensitivity to particular drugs, while others could lead to diminished responsiveness. Additionally, specific gene polymorphisms could elevate the risk of adverse effects in some patients but not in others. This underscores the necessity of personalized medicine strategies, where tailoring treatments based on an individual's genetic composition concerning the targeted TRPV variants can enhance therapeutic outcomes. However, this endeavor is not without its challenges. Personalized medicine introduces its own complexities and financial demands, which restrict accessibility for individuals and healthcare systems alike. These factors, in addition to the long development timelines, not only hinder the practical implementation of personalized treatments, but also complicate the creation of the necessary drugs.

Research has revealed that when TRPV channels are blocked or manipulated, the body responds by attempting to regain its normal function. This was evident in a clinical trial involving AMG 517, a specific TRPV1 antagonist administrated to mitigate pain. Notably, since this antagonist does not hinder heat-induced receptor activation, the suppression of TRPV1 led to hyperthermia in humans, a pattern similarly observed in rats, dogs, and monkeys [164]. This notion finds support in a separate study using SB-705498, a compound that antagonizes all modalities of TRPV1 activation, where no hyperthermia was observed [165]. This compelling evidence could potentially indicate how compensatory mechanisms played a role in causing hyperthermia in the first study, in contrast to the second one. Consequently, another concern arises, pertaining to the gradual decline in cells’ sensitivity to TRPV-targeted drugs over time. This development of tolerance and desensitization could lead to a diminished therapeutic response, potentially necessitating elevated drug doses for comparable effects or causing a decline in treatment effectiveness. Consequently, this poses a challenge for pharmaceutical companies to create enduring and safe drugs. Furthermore, compensatory responses can differ among individuals, reigniting the concerns associated with personalized medicine discussed earlier.

Finally, emerging evidence in the field of TRPV channel research brings to light the intricacies of these channels’ functions, posing both opportunities and challenges for therapeutic interventions. As our understanding of TRPV channels’ roles continues to evolve, the potential for unexpected interactions and off-target effects becomes a significant challenge. These channels are found in various tissues throughout the body, and as new roles are uncovered, the risk of unintended consequences when targeting them for therapy increases. Emerging research might reveal that a TRPV channel assumes a role not solely within the intended therapeutic pathway but also in other unforeseen systems, leading to unpredicted outcomes. This underscores the importance of comprehensive exploration, cautious therapeutic design, and constant adaptation as we navigate the evolving landscape of TRPV channels functions in the pursuit of effective and safe treatments.

8. Conclusions

In conclusion, TRPV channels, being extensively distributed throughout the GIT, assume crucial roles in its function and are thus subject to tight regulation. TRPV channels are integral in governing both normal physiological functions and pathological conditions. In normal body physiology, they modulate gut motility, secretions, and nutrient absorption. Conversely, in pathological conditions, they contribute to gut pain sensation and inflammation. TRPV channels are also involved in key cellular processes, such as proliferation and migration, which are critical in both ulcer formation and mucosal healing. Hence, their involvement underscores the therapeutic potential of targeting TRPV channels for treating GI disorders. Moreover, TRPV channels have been associated with various GI tumors, presenting potential breakthrough targets for innovative cancer therapies. Nonetheless, several challenges hinder the clinical application of TRPV-targeted therapies. These include potential unintended systemic effects due to their widespread distribution, altered responses to different stimuli, loss of essential physiological roles, compensatory mechanisms following channel antagonism, and the necessity of a personalized approach to therapy. Despite significant progress, important gaps remain. Future studies should aim to clarify the cell-type-specific and context-dependent roles of TRPV channels, better delineate the systemic consequences of TRPV modulation, and develop more selective modulators and targeted delivery systems. It will also be important to account for patient-specific factors that may influence therapeutic responses. Addressing these gaps will be critical to fully harnessing the therapeutic potential of TRPV channels and translating experimental insights into effective, safe, and personalized interventions for gastrointestinal disease.