Télémaque S, D'Orléans-Juste P
Department of Pharmacology, School of Medicine, University of Sherbrooke, Quebec, Canada.
Naunyn Schmiedebergs Arch Pharmacol. 1991 Oct;344(4):505-7. doi: 10.1007/BF00172593.
Endothelin-1 (ET-1) enhanced field stimulation-evoked (0.1 Hz), nerve-mediated contractions of the prostatic portion of the rat vas deferens. The human precursor of ET-1, big-endothelin (1-38) (big-ET-1) was only two-fold less potent than ET-1 (pD2 values: 7.30 and 7.49, respectively). The threshold concentrations necessary to elicit an increase of the response to electrical stimulation was lower for ET-1 (5 nmol/l) than for big-ET-1 (25 nmol/l). Endothelin-3 (ET-3) also markedly enhanced the response of the tissue to field stimulation with a potency similar to ET-1 (pD2 value: 7.59). In contrast, the precursor of ET-3, big-endothelin (1-41) (big-ET-3), was inactive at concentrations up to 0.5 mumol/l. Treatment of the preparations with phosphoramidon (50 mumol/l) markedly reduced the twitch enhancement by big-ET-1 without affecting the response to ET-1. Our results suggest the presence of a specific phosphoramidon-sensitive endothelin-converting enzyme which converts big-ET-1 to ET-1 in the rat vas deferens.
内皮素 -1(ET -1)增强了大鼠输精管前列腺部由场刺激诱发(0.1赫兹)的神经介导收缩。ET -1的人类前体,大内皮素(1 - 38)(big - ET -1)的效力仅比ET -1低两倍(pD2值分别为7.30和7.49)。引发对电刺激反应增强所需的阈浓度,ET -1(5纳摩尔/升)低于big - ET -1(25纳摩尔/升)。内皮素 -3(ET -3)也显著增强了组织对场刺激的反应,其效力与ET -1相似(pD2值:7.59)。相比之下,ET -3的前体,大内皮素(1 - 41)(big - ET -3)在浓度高达0.5微摩尔/升时无活性。用磷酰胺(50微摩尔/升)处理制剂可显著降低big - ET -1引起的抽搐增强,而不影响对ET -1的反应。我们的结果表明,在大鼠输精管中存在一种特定的对磷酰胺敏感的内皮素转换酶,它可将big - ET -1转化为ET -1。