Mepivacaine-induced contraction is attenuated by endothelial nitric oxide release in isolated rat aorta |
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Authors: | Sung Hui-Jin Choi Mun-Jeoung Ok Seong-Ho Lee Soo Hee Hwang Il Jeong Kim Hee Sook Chang Ki Churl Shin Il-Woo Lee Heon-Keun Park Kyeong-Eon Chung Young-Kyun Sohn Ju-Tae |
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Institution: | Department of Anesthesiology, Charmjoeun Obstetrics and Gynecology Clinic, Jinju, Korea. |
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Abstract: | Mepivacaine is an aminoamide-linked local anesthetic with an intermediate duration that intrinsically produces vasoconstriction both in vivo and in vitro. The aims of this in-vitro study were to examine the direct effect of mepivacaine in isolated rat aortic rings and to determine the associated cellular mechanism with a particular focus on endothelium-derived vasodilators, which modulate vascular tone. In the aortic rings with or without endothelium, cumulative mepivacaine concentration-response curves were generated in the presence or absence of the following antagonists: N(ω)-nitro-L-arginine methyl ester L-NAME], indomethacin, fluconazole, methylene blue, 1H-1,2,4]oxadiazolo4,3-a]quinoxalin-1-one ODQ], verapamil, and calcium-free Krebs solution. Mepivacaine produced vasoconstriction at low concentrations (1 × 10(-3) and 3 × 10(-3) mol/L) followed by vasodilation at a high concentration (1 × 10(-2) mol/L). The mepivacaine-induced contraction was higher in endothelium-denuded aortae than in endothelium-intact aortae. Pretreatment with L-NAME, ODQ, and methylene blue enhanced mepivacaine-induced contraction in the endothelium-intact rings, whereas fluconazole had no effect. Indomethacin slightly attenuated mepivacaine-induced contraction, whereas verapamil and calcium-free Krebs solution more strongly attenuated this contraction. The vasoconstriction induced by mepivacaine is attenuated mainly by the endothelial nitric oxide - cyclic guanosine monophosphate pathway. In addition, mepivacaine-induced contraction involves cyclooxygenase pathway activation and extracellular calcium influx via voltage-operated calcium channels. |
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