Satoh M, Takada M, Ohshima N, Takayanagi I, Koike K
Department of Chemical Pharmacology, Toho University School of Pharmaceutical Sciences, Funabashi, Chiba, Japan.
Biol Pharm Bull. 1998 Jul;21(7):718-22. doi: 10.1248/bpb.21.718.
We observed endothelin (ET)-induced contractile responses on prostatic and epididymal segments, as well as the facilitation of an electrically stimulated tone on prostatic segments of isolated rat vas deferens. In both segments, the selective ET(B)-receptor agonists, IRL 1620 and sarafotoxin S6c, produced only a small contraction or no contraction at a concentration of 1 microM. The rank order of contraction potencies (pD2 value) was ET-1 = ET-2 > ET-3 >> sarafotoxin S6c = IRL 1620. The maximum responses of ET-induced contractions in the prostatic segments were larger than those in the epididymal segments. The contractile response to ET-3 was antagonized by pretreatment for 30 min with BQ-123 (10 nM), a selective ET(A) receptor antagonist, and BQ-788 (1 microM), a selective ET(B) receptor antagonist. The contractile responses to ET-1 were antagonized by pretreatment with BQ-123 (10 microM), but not with BQ-788 (1 microM). The ET-3-induced facilitation on the twitch response to electrical stimulation in the prostatic segment of the vas deferens was antagonized by BQ-123 (0.1 microM) and BQ-788 (1 microM). The ET-1-induced facilitation was antagonized by pretreatment with BQ-123 (3 microM), but not with BQ-788 (10 microM). These results suggest that in rat vas deferens the ET(A) receptors are divided into BQ-123-sensitive ET(A1) and BQ-123-insensitive ET(A2) subtypes, and the production of a contractile response of smooth muscle as well as the facilitation of neurotransmission are accomplished through mediation by ET(A1)- and ET(A2)-subtypes.
我们观察到内皮素(ET)对前列腺和附睾段的收缩反应,以及对离体大鼠输精管前列腺段电刺激张力的促进作用。在这两个段中,选择性ET(B)受体激动剂IRL 1620和蛙皮素S6c在1 microM浓度下仅产生微小收缩或无收缩。收缩效力(pD2值)的顺序为ET-1 = ET-2 > ET-3 >> 蛙皮素S6c = IRL 1620。ET诱导的前列腺段收缩的最大反应大于附睾段。用选择性ET(A)受体拮抗剂BQ-123(10 nM)和选择性ET(B)受体拮抗剂BQ-788(1 microM)预处理30分钟可拮抗对ET-3的收缩反应。用BQ-123(10 microM)预处理可拮抗对ET-1的收缩反应,但用BQ-788(1 microM)则不能。BQ-123(0.1 microM)和BQ-788(1 microM)可拮抗ET-3对输精管前列腺段电刺激抽搐反应的促进作用。用BQ-123(3 microM)预处理可拮抗ET-1诱导的促进作用,但用BQ-788(10 microM)则不能。这些结果表明,在大鼠输精管中,ET(A)受体分为BQ-123敏感的ET(A1)和BQ-123不敏感的ET(A2)亚型,平滑肌收缩反应的产生以及神经传递的促进是通过ET(A1)和ET(A2)亚型介导完成的。