Version 1
: Received: 25 May 2017 / Approved: 26 May 2017 / Online: 26 May 2017 (04:52:12 CEST)
How to cite:
Sha, Y.; Zhang, Y.; Cao, J.; Qian, K.; Niu, B.; Chen, Q. Insulin Secretion with the Effect of Loureirin B through KATP Channel–Dependent Pathway. Preprints2017, 2017050189. https://doi.org/10.20944/preprints201705.0189.v1
Sha, Y.; Zhang, Y.; Cao, J.; Qian, K.; Niu, B.; Chen, Q. Insulin Secretion with the Effect of Loureirin B through KATP Channel–Dependent Pathway. Preprints 2017, 2017050189. https://doi.org/10.20944/preprints201705.0189.v1
Sha, Y.; Zhang, Y.; Cao, J.; Qian, K.; Niu, B.; Chen, Q. Insulin Secretion with the Effect of Loureirin B through KATP Channel–Dependent Pathway. Preprints2017, 2017050189. https://doi.org/10.20944/preprints201705.0189.v1
APA Style
Sha, Y., Zhang, Y., Cao, J., Qian, K., Niu, B., & Chen, Q. (2017). Insulin Secretion with the Effect of Loureirin B through K<sub>ATP </sub>Channel–Dependent Pathway. Preprints. https://doi.org/10.20944/preprints201705.0189.v1
Chicago/Turabian Style
Sha, Y., Bing Niu and Qin Chen. 2017 "Insulin Secretion with the Effect of Loureirin B through K<sub>ATP </sub>Channel–Dependent Pathway" Preprints. https://doi.org/10.20944/preprints201705.0189.v1
Abstract
The development of new diabetes drugs continues to be explored. Loureirin B, a flavonoid, extracted from Dracaena cochinchinensis, has been confirmed to increase insulin secretion and decrease blood glucose levels. For understanding the mechanism, a series of experiments had been employed based on computational methods and cell experiments. The insulin secretion significantly increased with the incubation of 0.01μM loureirin B for 4 hours. The viability of Ins-1 cells showed no significant difference with the treatment of loureirin B. Through computational methods, we hypothesized that loureirin B could interacts with KATP channels to promote insulin secretion. In cell experiments, it could be found that the current of KATP channel of Ins-1 cells was inhibited by the effect of loureirin B. After then, the voltage-dependent calcium channels were activated, the increase of Cx43 protein expression might mediate the Ca2+ to the intracellular. In summary, it could be concluded that loureirin B promoted insulin secretion mainly through inhibiting KATP current, the influx of Ca2+ to the Intracellular and the expression of Cx43.
Keywords
loureirin B; Ins-1 cells; Insulin secretion; KATP channel; influx of Ca2+; expression of Cx43
Subject
Biology and Life Sciences, Biochemistry and Molecular Biology
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
