首页> 外文期刊>European Journal of Pharmacology: An International Journal >Cooling augments vasoconstriction mediated by 5-HT(1) and alpha(2)-adrenoceptors in the isolated equine digital vein: involvement of Rho kinase.
【24h】

Cooling augments vasoconstriction mediated by 5-HT(1) and alpha(2)-adrenoceptors in the isolated equine digital vein: involvement of Rho kinase.

机译:冷却增强了孤立的马数字静脉中5-HT(1)和α(2)-肾上腺素受体介导的血管收缩:Rho激酶的参与。

获取原文
获取原文并翻译 | 示例
       

摘要

The vasculature of the equine digit fulfils an important role in thermoregulation. In other species, it has been found that cooling may enhance the response of cutaneous vessels to 5-hydroxytryptamine (5-HT) and alpha(2)-adrenoceptor agonists. Translocation of alpha(2)-adrenoceptors to the smooth muscle cell membrane, mediated by Rho kinase, is thought to be involved in the cooling-enhanced response in mouse tail arteries. However, little is known about the effect of cooling on 5-HT receptor function. The present investigation compared the response of 5-bromo-6-(2-imidazolin-2-ylamino) quinoxaline (UK14304:1 nM to 30 muM), methoxamine (0.1 nM to 30 muM; in the presence of yohimbine 0.1 muM), 5-carboxamidotryptamine (5-CT; 0.1 nM to 10 muM) and alpha-methyl 5-HT (0.1 nM to 10 muM) in the isolated equine digital vein at 30 degrees C and 22 degrees C. The effect of the Rho kinase inhibitor, fasudil (1 muM), and the recovery of the response after the irreversible blockade of surface receptors with phenoxybenzamine (10 muM) or 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ;10 muM), was established. Moderate cooling significantly increased the maximum response to alpha-methyl 5-HT, 5-CT and UK14304 and shifted their response curves to the left. Cooling also augmented the phenoxybenzamine- and EEDQ-resistant response to UK14304 and 5-CT, respectively. Fasudil had no effect on the contractile response at 30 degrees C, but completely abrogated the effect of cooling on the response to 5-CT and UK14304. The response to methoxamine was not significantly affected by cooling. These results suggest that Rho kinase plays an important role in the cooling-enhanced response mediated by 5-HT(1B/D) receptors and alpha(2)-adrenoceptors. The exact mechanism by which Rho/Rho kinase enhances the functional responses mediated by these receptors in these vessels has yet to be determined.
机译:马手指的脉管系统在温度调节中起重要作用。在其他物种中,已经发现冷却可以增强皮肤血管对5-羟色胺(5-HT)和α(2)-肾上腺素受体激动剂的反应。由Rho激酶介导的α(2)-肾上腺素受体向平滑肌细胞膜的转运被认为与小鼠尾动脉的冷却增强反应有关。然而,关于冷却对5-HT受体功能的影响知之甚少。本研究比较了5-溴-6-(2-咪唑啉-2-基氨基)喹喔啉(UK14304:1 nM至30μM),甲氧胺(0.1 nM至30μM;在育亨宾0.1μM存在下)的响应,在30°C和22°C的分离的马数字静脉中产生5-羧酰胺基色胺(5-CT; 0.1 nM至10μM)和α-甲基5-HT(0.1 nM至10μM).Rho激酶抑制剂的作用,法舒地尔(1μM),以及用苯氧基苯甲胺(10μM)或2-乙氧基-1-乙氧基羰基-1,2-二氢喹啉(EEDQ; 10μM)不可逆转地阻断表面受体后,恢复反应。适度冷却显着提高了对α-甲基5-HT,5-CT和UK14304的最大响应,并将其响应曲线向左移动。冷却还分别增强了对UK14304和5-CT的耐苯氧基苯甲胺和EEDQ的反应。法舒地尔对30摄氏度的收缩反应没有影响,但完全消除了冷却对5-CT和UK14304的反应的影响。冷却对甲氧胺的反应没有显着影响。这些结果表明,Rho激酶在由5-HT(1B / D)受体和alpha(2)-肾上腺素受体介导的冷却增强应答中起重要作用。 Rho / Rho激酶增强这些血管中这些受体介导的功能反应的确切机制尚未确定。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号