Submitted:
08 September 2025
Posted:
09 September 2025
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Abstract
Keywords:
1. Introduction
2. Fundamentals and Action Mechanism
- i.
- Cellular Light Absorption and Primary Chromophores. The main intracellular chromophore targeted by BMF is CcO, located in the mitochondrial electron transport chain. Light absorption by this enzyme induces an increase in ATP production, a transient increase in reactive oxygen species (ROS), and the release of NO [1]. NO, when displaced from CcO, allows for greater respiratory efficiency, thus improving cellular energy production [24].
- ii.
- Activation of intracellular signaling pathways. Increased mitochondrial activity triggers cellular signaling pathways such as PI3K/AKT, MAPK/ERK, and NF-κB, which are involved in processes such as cell proliferation, protein synthesis, and the inhibition of apoptosis [23,25]. Activation of the PI3K/AKT system is particularly relevant for the migration and proliferation of fibroblasts, endothelial cells, and keratinocytes [26].
- iii.
- Stimulation of angiogenesis. PBM also promotes angiogenesis through the activation of the VEGF/VEGFR2/STAT3 pathway. This pathway has been implicated in the nuclear translocation of growth factors, which stimulate the formation of new blood vessels, essential for tissue regeneration in surgical wounds [23].
- iv.
- Modulation of oxidative stress and inflammatory processes. The controlled release of ROS during PBM acts as a cellular second messenger, regulating inflammatory processes. A reduction in the expression of proinflammatory cytokines such as -6 and TNF-α, and an increase in IL-10, an anti-inflammatory cytokine, has been observed, facilitating a more rapid resolution of the post-surgical inflammatory process [22].
- v.
- Regulation of Intracellular Calcium and Ion Channels. Voltage-gated calcium channels and TRP channels have also been identified as targets of BMF. Modulation of these channels can impact muscle contraction, neuronal signaling, and cell secretion [24].
- vi.
- Promotion of Cell Differentiation and Proliferation. In the presence of growth factors, such as platelet-rich plasma, BMF enhances cell proliferation and bone mineralization, as observed in osteoblastic cell lines and bone models [27].
- vii.
- viii.
- Application in in vivo animal models. Studies in rat and dog wound models have shown that PBM applied daily with 600-800 nm lasers accelerates wound closure, increases type I collagen expression, and improves tissue architecture [21]. In canines, PBM applied after dental procedures significantly reduced gingival inflammation [4].
- ix.
- Applications in the nervous and musculoskeletal systems. PBM has also been shown to be effective in pain modulation and nerve recovery, especially in cases of intervertebral disc disease in dogs, by targeting spinal cord inflammation and promoting axonal regeneration [28,29]. However, the biological response to PBM follows a dose-response curve in the form of a “therapeutic window,” where low doses are biostimulatory, but high doses can be inhibitory or even harmful [30].
3. Clinical Evidence in Veterinary Surgery
3.1. Wound Healing and Tissue Regeneration
Preclinical Experimental Studies
Clinical Evidence in Domestic Animals
Effective Protocols and Optimal Parameters
3.2. Postoperative Pain Control
Mechanisms Involved in PBM-Induced Analgesia
Clinical Evidence in Canines and Felines
Barriers to Clinical Practice and Pain Perception
Equine and Other Species Surgery
3.3. Safety and Adverse Effects in Veterinary Surgery
General Security Profile
Considerations According to Type of Laser and Class of Equipment
Contraindications and precautions in the application of PBM.
- ○
- Active neoplasia: Applying PBM directly to tumors is not recommended, as there is uncertainty about its proliferative effect on neoplastic cells [57].
- ○
- Thyroid gland: Direct irradiation of this area should be avoided, especially in growing animals or those with hormonal disorders, due to potential effects on thyroid function [33].
- ○
- Pregnancy: There is insufficient evidence to support safety in developing fetuses, so caution is recommended in pregnant females [58].
Reported Adverse Effects
- ○
- Local hyperemia or mild heat after prolonged exposure or with improperly applied high-power devices [60].
- ○
- Transient increase in pain in areas of intense acute inflammation, likely due to superficial nerve activation before modulation [36].
- ○
- Patient restlessness or refusal, especially in areas with cutaneous hypersensitivity [50].
3.4. Specific Applications in Veterinary Surgery
Orthopedic Surgery
Oral Surgery and Dentistry
Soft Tissue Surgery
Neurosurgery
3.5. Limitations and Challenges in the Clinical Application of PBM in Veterinary Surgery
Variability in Application Protocols
Small Sample Size and Heterogeneity of Studies
Lack of Blinding and Adequate Control Groups
Difficulty in Objective Evaluation of Results
Initial Cost of Equipment and Specific Training Required
Low Inclusion in Clinical Guidelines and Lack of Legal Recognition
4. Relevant Technical Parameters in PBM Applied to Veterinary Surgery
4.1. Wavelength
- ○
- 630–660 nm (visible red): Good absorption by CcO, useful for skin and superficial wounds.
- ○
- 800–980 nm (near-infrared (NIR)): Greater penetration, recommended for joints, deep muscles, and subcutaneous tissues.
4.2. Power and Irradiance
- -
- Typical power levels: 30 mW–3 W.
- -
- Recommended irradiance: <100 mW/cm2 to avoid cellular overheating and maintain photobiomodulatory effects without thermal damage.
4.3. Energy and Energy Density (Fluence)
4.4. Exposure Time and Frequency
- -
- Time per application point: 10 to 120 seconds, depending on the intensity and size of the irradiated area.
- -
- Treatment frequency: Daily or every other day for acute protocols; 2–3 times per week for chronic treatments.
- -
- Total number of sessions: Varies between 3 and 10 in postoperative treatments, longer for chronic or degenerative diseases.
4.5. Emission form (Continuous vs. Pulsed)
- -
- Continuous mode: generates constant stimulation, greater thermal accumulation, and is useful for direct mitochondrial stimulation [72].
- -
4.6. Beam Size and Tissue Characteristics
- ○
- Small areas: require precision and lower power.
- ○
- Deep tissue or dense hair: require more power or pre-shaving to allow for better transmission.
5. Future Perspectives and Emerging Research
6. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
Abbreviations
| AI | Artificial intelligence |
| ATP | Adenosine triphosphate |
| CcO | Cytochrome c oxidase |
| COX-2 | Cyclooxygenase-2 |
| J | Joules |
| LLLT | Low-level laser therapy |
| NIR | Near infrared |
| nm | Nanometers |
| NO | Nitric oxide |
| PBM | Photobiomodulation |
| PS | Post-Surgical |
| ROS | Reactive oxygen species |
| TPLO | Tibial plate leveling osteotomy |
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| Clinic application1,3 | Wavelength (nm) | Energy density (J/cm2) | Emission form | Frequency | N. of sessions | Additional comments |
|---|---|---|---|---|---|---|
| Healing of surgical wounds | 630-660 (red) / 810-980 (NIR) | 4-8 | Continuous or pulsed | 1 time/day PS | 5-7 | Ideally within 48h PS |
| Postoperative soft tissue pain | 810–980 | 6-12 | Pulsed | 1 time/day | 3-5 | With conventional analgesia |
| Orthopedic surgery | 980 | 10-20 | Pulsed | 2-3 times/week | 6-10 | Shave2 for better penetration |
| Oral surgery / dentistry | 630-660 | 3-6 | Continuous | Immediate PS | 3-5 | With conventional analgesia |
| Joint or perilesional inflammation | 810-980 | 8-15 | Pulsed | 2 times/week | According to evolution | Monitor clinical response |
| Neurosurgery / spinal cord injury | 810-850 | 8-10 | Pulsed | Daily | Up to 2 weeks | Data still preliminary |
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