Hadj-Kaddour K, Michel A, Chevillard C
Laboratoire de Pharmacodynamie, Faculté de Pharmacie, Montpellier, France.
Eur J Pharmacol. 1996 Mar 7;298(2):145-8. doi: 10.1016/0014-2999(95)00760-1.
The effects of endothelin-1 and endothelin-3 were investigated on carbachol-contracted guinea-pig isolated trachea. Endothelin-1 and endothelin-3 (0.1-100 nM) induced partial dose-dependent relaxation of the precontracted preparations. The endothelin-1-induced relaxation was markedly attenuated by haemoglobin (10 microM) and methylene blue (10 microM) and by epithelium removal. In contrast, endothelin-3-induced relaxation was not affected by haemoglobin, methylene blue or epithelium removal. The large conductance Ca(2+)-activated K(+)-channel blocker, charybdotoxin, antagonized the endothelin-1- and the endothelin-3-induced relaxation to the same extent. These results show that both endothelin-1 and endothelin-3 relaxant activities are modulated by charybdotoxin-sensitive K(+)-channels, while the nitric oxide pathway is only involved in endothelin-1 relaxant effects.
研究了内皮素 -1和内皮素 -3对卡巴胆碱收缩的豚鼠离体气管的影响。内皮素 -1和内皮素 -3(0.1 - 100 nM)可诱导预收缩制剂出现部分剂量依赖性舒张。血红蛋白(10 μM)、亚甲蓝(10 μM)以及去除上皮可显著减弱内皮素 -1诱导的舒张。相比之下,内皮素 -3诱导的舒张不受血红蛋白、亚甲蓝或去除上皮的影响。大电导钙激活钾通道阻滞剂蝎毒素能同等程度地拮抗内皮素 -1和内皮素 -3诱导的舒张。这些结果表明,内皮素 -1和内皮素 -3的舒张活性均受蝎毒素敏感的钾通道调节,而一氧化氮途径仅参与内皮素 -1的舒张作用。