Kamata K, Miyata N, Kasuya Y
Department of Pharmacology, School of Pharmacy, Hoshi University, Tokyo, Japan.
Gen Pharmacol. 1990;21(1):127-9. doi: 10.1016/0306-3623(90)90607-n.
The effects of endothelin, a novel potent vasoconstrictor peptide, on isolated portal veins were examined in spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY). Endothelin contarcted the portal vein from SHR and WKY, in a concentration-dependent manner. However, both twitch contraction and tonic contraction of portal veins in response to endothelin were significantly enhanced in SHR. In contrast to the effects of endothelin, twitch contractile responses to Bay K 8644 were not significantly different between vessels from SHR and WKY. These results indicate that endothelin is a potent vasoconstrictor peptide in the portal vein, and that the increased sensitivity in SHR may be due to an increase in the activity of voltage-dependent Ca2+ channels which is modulated by endothelin, but not to an increase in the activity of voltage-dependent Ca2+ channels which can be stimulated by Bay K 8644.
在自发性高血压大鼠(SHR)和Wistar Kyoto大鼠(WKY)中,研究了一种新型强效血管收缩肽内皮素对离体门静脉的作用。内皮素使SHR和WKY的门静脉收缩,且呈浓度依赖性。然而,SHR中门静脉对内皮素的抽动收缩和强直收缩均显著增强。与内皮素的作用相反,SHR和WKY血管对Bay K 8644的抽动收缩反应无显著差异。这些结果表明,内皮素是门静脉中的一种强效血管收缩肽,SHR中敏感性增加可能是由于内皮素调节的电压依赖性Ca2+通道活性增加,而非Bay K 8644刺激的电压依赖性Ca2+通道活性增加。