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Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels

Year 2024, Volume: 28 Issue: 5, 1501 - 1507, 28.06.2025

Abstract

Mammals have approximately 80 genes that encode potassium (K+) channels. They have a wide range of physiological functions, such as modulation of action potential duration and relaxation of smooth muscles. Carvacrol, a compound found in various aromatic plants, has been used traditionally for treating asthma, menstrual spasms, and gastrointestinal disorders. However, its mechanism of action on smooth muscles remains insufficiently understood. This study investigates the role of potassium ion channels in the relaxing effects of carvacrol on isolated rat duodenum smooth muscles. Rats were euthanized and duodenal segments were prepared and placed in an isolated organ bath with Krebs’ solution. The segments were equilibrated for 1 h and then treated with chemicals to obtain concentration-response curves. The data were evaluated using one-way Analysis of Variance (ANOVA) and Tukey's Honest Significant Difference (Tukey’s HSD) test for multiple comparisons. Our findings demonstrate that carvacrol induces a dose-dependent relaxation of these muscles. The relaxation effects were significantly reduced in the presence of specific potassium channel inhibitors, including paxilline, UCL1684, linopirdine, barium chloride, and 4-aminopyridine. They were completely blocked by the combination of barium chloride and tetraethylammonium. However, glibenclamide, ruthenium red, and nitroarginine did not alter the relaxing effects of carvacrol. In conclusion: carvacrol relaxes duodenum smooth muscles by opening barium chloride-sensitive Kir2.1 and Kir3.1, as well as tetraethylammonium-sensitive KCa1.1, KCa2.1, KCa2.2, KCa2.3, Kv1.2, Kv1.4, Kv1.5, Kv2.1, Kv2.2, Kv4.1, Kv4.2, Kv4.3, Kv7.1, Kv7.2, Kv7.3, Kv7.4, and Kv7.5 potassium channels.

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There are 37 citations in total.

Details

Primary Language English
Subjects Basic Pharmacology
Journal Section Articles
Authors

Muhammed Yusuf 0000-0003-2807-7985

Süleyman Aydın 0000-0002-4052-8470

Publication Date June 28, 2025
Submission Date July 9, 2024
Acceptance Date July 27, 2024
Published in Issue Year 2024 Volume: 28 Issue: 5

Cite

APA Yusuf, M., & Aydın, S. (2025). Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels. Journal of Research in Pharmacy, 28(5), 1501-1507.
AMA Yusuf M, Aydın S. Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels. J. Res. Pharm. July 2025;28(5):1501-1507.
Chicago Yusuf, Muhammed, and Süleyman Aydın. “Relaxing Actions of Carvacrol on Isolated Rat Duodenum Smooth Muscles: Evidence for the Role of Potassium Ion Channels”. Journal of Research in Pharmacy 28, no. 5 (July 2025): 1501-7.
EndNote Yusuf M, Aydın S (July 1, 2025) Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels. Journal of Research in Pharmacy 28 5 1501–1507.
IEEE M. Yusuf and S. Aydın, “Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels”, J. Res. Pharm., vol. 28, no. 5, pp. 1501–1507, 2025.
ISNAD Yusuf, Muhammed - Aydın, Süleyman. “Relaxing Actions of Carvacrol on Isolated Rat Duodenum Smooth Muscles: Evidence for the Role of Potassium Ion Channels”. Journal of Research in Pharmacy 28/5 (July2025), 1501-1507.
JAMA Yusuf M, Aydın S. Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels. J. Res. Pharm. 2025;28:1501–1507.
MLA Yusuf, Muhammed and Süleyman Aydın. “Relaxing Actions of Carvacrol on Isolated Rat Duodenum Smooth Muscles: Evidence for the Role of Potassium Ion Channels”. Journal of Research in Pharmacy, vol. 28, no. 5, 2025, pp. 1501-7.
Vancouver Yusuf M, Aydın S. Relaxing actions of carvacrol on isolated rat duodenum smooth muscles: Evidence for the role of potassium ion channels. J. Res. Pharm. 2025;28(5):1501-7.