Antioxidant Activity And Stress-Protective Mechanisms Of Bile Acid Derivatives In Rat Aorta
Keywords:
bile acid derivatives, ursodeoxycholic acid, taurocholic acid, rat aorta, smooth muscle, vasorelaxation, nitric oxide synthesis, calcium channels, myography, antioxidant activityAbstract
This study investigates the effects of bile acid derivatives — ursodeoxycholic acid (UDCA) and taurocholic acid (TCA) — on the contractile activity of smooth muscles in the rat aorta. The research confirmed that both compounds induce dose-dependent vasorelaxation, and their mechanisms of action were analyzed in detail. The vasodilatory effect of UDCA was found to be associated with nitric oxide (NO) synthesis via the endothelium, while TCA’s effect was attributed to the restriction of calcium ion influx into cells. The sensitivity of phenylephrine-induced smooth muscle contraction to these substances was assessed using myographic methods. The results suggest that UDCA and TCA may serve as potential natural therapeutic agents for cardiovascular diseases.
References
Zhao, Y., Zhang, L., Wang, S., et al. (2016). Ursodeoxycholic acid stimulates nitric oxide production and protects endothelial function in rats. European Journal of Pharmacology, 789, 34–42. https://doi.org/10.1016/j.ejphar.2016.06.023
Kim, H. J., Lee, J. H., Park, E. J., et al. (2021). Inhibitory effects of ursodeoxycholic acid on calcium influx in vascular smooth muscle cells. Biomedicine & Pharmacotherapy, 138, 111504. https://doi.org/10.1016/j.biopha.2021.111504
Lee, M. J., Kim, S. H., Cho, H. J. (2018). Differential effects of bile acid derivatives on vascular relaxation in rat aorta. Vascular Pharmacology, 106, 16–23. https://doi.org/10.1016/j.vph.2018.02.003
Rodríguez, R. M., et al. (2020). Taurocholic acid modulates vascular tone via FXR-dependent pathways in isolated rat arteries. Frontiers in Physiology, 11, 124. https://doi.org/10.3389/fphys.2020.00124
Sies, H., & Jones, D. P. (2020). Reactive oxygen species (ROS) as pleiotropic physiological signalling agents. Nature Reviews Molecular Cell Biology, 21(7), 363–383. https://doi.org/10.1038/s41580-020-0230-3
Bernardi, M., et al. (2011). Ursodeoxycholic acid in the treatment of liver diseases: a review of its pharmacological properties and clinical use. Drugs, 71(9), 1201–1228. https://doi.org/10.2165/11589410-000000000-00000
Lapenna, D., et al. (1998). Antioxidant properties of ursodeoxycholic acid. Biochemical Pharmacology, 56(3), 331–336. https://doi.org/10.1016/S0006-2952(98)00112-1
Halliwell, B., & Gutteridge, J. M. C. (2015). Free Radicals in Biology and Medicine (5th ed.). Oxford University Press.
Nrf2–Keap1 signaling pathway and cardiovascular diseases: role in redox homeostasis and inflammation – Zhang, D. D. (2017). Cardiovascular Research, 114(5), 653–665. https://doi.org/10.1093/cvr/cvx020.