Nishiyama M, Moroi K, Shan L H, Yamamoto M, Takasaki C, Masaki T, Kimura S
Division of Cardiovascular Biology, Chiba University School of Medicine, Japan.
Jpn J Pharmacol. 1995 Jul;68(3):235-43. doi: 10.1254/jjp.68.235.
To study endothelin receptor subtypes that mediate venous smooth muscle contraction, effects of some endothelin receptor agonists and antagonists on the rabbit lateral saphenous vein were examined and compared with those on the saphenous artery. In the artery, endothelin (ET)-1 elicited concentration-dependent contractions, while selective ETB-receptor agonists, IRL1620 (Suc-[Glu9,Ala11,15]ET-1(8-21)) and sarafotoxin 6c (S6c) had almost no effect. The ET-1-induced responses shifted in parallel to the right by BQ-123 (cyclo (-D-Trp-D-Asp-Pro-D-Val-Leu-)), an ETA-receptor antagonist, or PD142893 (Ac-D-Dip-Leu-Asp-Ile-Ile-Trp), an ETA/ETB-receptor antagonist, indicating the involvement of the ETA receptor in this response. In the saphenous vein, not only ET-1 and ET-3, but also ETB-receptor agonists, IRL1620, S6c and [Glu9]sarafotoxin 6b ([Glu9]S6b), produced concentration-dependent, BQ-123-insensitive contractions. PD142893 did not affect the ET-1-induced contraction, but it shifted greatly the IRL1620-induced concentration-response curve in parallel to the right. The major components of ET-3-, S6c- and [Glu9]S6b-induced contractions were resistant to PD142893. These results indicate that two different vasoconstrictive ETB-receptor subtypes, ETB1 (sensitive to IRL1620 and PD142893) and ETB2 (insensitive to IRL1620 and PD142893), are located on the smooth muscle of the saphenous vein.
为研究介导静脉平滑肌收缩的内皮素受体亚型,检测了一些内皮素受体激动剂和拮抗剂对兔隐静脉的作用,并与它们对隐动脉的作用进行比较。在动脉中,内皮素(ET)-1引起浓度依赖性收缩,而选择性ETB受体激动剂IRL1620(Suc-[Glu9,Ala11,15]ET-1(8-21))和沙拉毒素6c(S6c)几乎没有作用。ET-1诱导的反应被ETA受体拮抗剂BQ-123(环(-D-色氨酸-D-天冬氨酸-脯氨酸-D-缬氨酸-亮氨酸-))或ETA/ETB受体拮抗剂PD142893(Ac-D-二苯丙氨酸-亮氨酸-天冬氨酸-异亮氨酸-异亮氨酸-色氨酸)平行右移,表明ETA受体参与了该反应。在隐静脉中,不仅ET-1和ET-3,而且ETB受体激动剂IRL1620、S6c和[Glu9]沙拉毒素6b([Glu9]S6b)都产生浓度依赖性、对BQ-123不敏感的收缩。PD142893不影响ET-1诱导的收缩,但它使IRL1620诱导的浓度-反应曲线平行右移很大。ET-3、S6c和[Glu9]S6b诱导的收缩的主要成分对PD142893有抗性。这些结果表明,两种不同的血管收缩性ETB受体亚型,ETB1(对IRL1620和PD142893敏感)和ETB2(对IRL1620和PD142893不敏感),位于隐静脉平滑肌上。