Lebel N, D'Orléans-Juste P, Fournier A, Sirois P
Department of Pharmacology, Faculty of Medicine, University of Sherbrooke, Québec, Canada.
J Cardiovasc Pharmacol. 1995;26 Suppl 3:S81-3.
We studied the pharmacologic effects of big endothelin-1 (big ET-1), big endothelin-2 (big ET-2), and big endothelin-3 (big ET-3), and characterized the enzyme involved in the conversion of the three peptides in guinea pig upper bronchus (GPUB). ET-1, ET-2 and ET-3 (0.1-300 nM) elicited similar concentration-dependent contractions of GPUB. Big ET-1 and big ET-2, but not big ET-3, also elicited potent concentration-dependent contractions of GPUB. The conversion of big ET-1 to ET-1 in the GPUB is sensitive to phosphoramidon but not to thiorphan or captopril. Phosphoramidon inhibited the conversion of big ET-2 to ET-2, thiorphan had minimal effect, and captopril was without effect. These results suggest that the putative endothelin-converting enzyme (ECE) is involved in the conversion of big ET-1 to ET-1 in GPUB and the conversion of big ET-2 to ET-2 by a nonselective enzymatic process.
我们研究了大内皮素-1(big ET-1)、大内皮素-2(big ET-2)和大内皮素-3(big ET-3)的药理作用,并对豚鼠上支气管(GPUB)中参与这三种肽转化的酶进行了特性分析。ET-1、ET-2和ET-3(0.1 - 300 nM)引起了类似的GPUB浓度依赖性收缩。Big ET-1和big ET-2,但不是big ET-3,也引起了GPUB强烈的浓度依赖性收缩。在GPUB中,big ET-1向ET-1的转化对磷酰胺敏感,但对硫磷酰胺或卡托普利不敏感。磷酰胺抑制big ET-2向ET-2的转化,硫磷酰胺影响最小,卡托普利则无作用。这些结果表明,假定的内皮素转化酶(ECE)通过非选择性酶促过程参与了GPUB中big ET-1向ET-1的转化以及big ET-2向ET-2的转化。