Suppr超能文献

去大脑自发性高血压大鼠中钾通道开放剂与交感神经系统之间的全身和局部血流动力学相互作用

Systemic and regional haemodynamic interactions between K+ channel openers and the sympathetic nervous system in the pithed SHR.

作者信息

Richer C, Mulder P, Doussau M P, Gautier P, Giudicelli J F

机构信息

Département de Pharmacologie, Faculté de Médecine Paris-Sud, Le Kremlin-Bicêtre, France.

出版信息

Br J Pharmacol. 1990 Jul;100(3):557-63. doi: 10.1111/j.1476-5381.1990.tb15846.x.

Abstract
  1. The interactions between two K+ channel openers, cromakalim and SR 44866 (infused i.v. at equihypotensive doses), and the sympathetic nervous system at the systemic and regional (mesentery, kidney, hindlimb) vascular levels were investigated in the pithed spontaneously hypertensive rat (SHR) by use of the pulsed Doppler technique. 2. The two K+ channel openers did not affect postsynaptic alpha 1- but slightly reduced postsynaptic alpha 2-adrenoceptor mediated systemic pressor and regional vasoconstrictor responses. 3. Both drugs significantly decreased the systemic pressor and regional vasoconstrictor responses elicited by spinal cord stimulation. These sympathoinhibitory effects were not homogeneously distributed among the different vascular beds, the decreasing rank order being: mesentery greater than kidney greater than hindlimb. Simultaneously, the spinal cord stimulation-induced tachycardia remained unaffected. 4. After treatment with K+ channel openers, restoration of initial blood pressure and vascular tone values by infusion of prostaglandin F2 alpha (PGF2 alpha) and vasopressin respectively did not affect and abolished the sympathoinhibitory effects of cromakalim and SR 44866. 5. We conclude that in SHRs the two K+ channel openers that we investigated exert similar sympathohibitory effects which affect some vascular beds more than others. These effects are not dependent upon the arterial blood pressure level and are most likely prejunctionally located.
摘要
  1. 采用脉冲多普勒技术,在脊髓横断的自发性高血压大鼠(SHR)中研究了两种钾通道开放剂——克罗卡林和SR 44866(以等降压剂量静脉输注)与全身及局部(肠系膜、肾脏、后肢)血管水平的交感神经系统之间的相互作用。2. 这两种钾通道开放剂不影响突触后α1 - 肾上腺素能受体介导的反应,但略微降低了突触后α2 - 肾上腺素能受体介导的全身升压和局部血管收缩反应。3. 两种药物均显著降低了脊髓刺激引起的全身升压和局部血管收缩反应。这些交感抑制作用在不同血管床中分布不均,降低程度的顺序为:肠系膜>肾脏>后肢。同时,脊髓刺激引起的心动过速不受影响。4. 用钾通道开放剂治疗后,分别输注前列腺素F2α(PGF2α)和血管加压素恢复初始血压和血管张力值,并未影响且消除了克罗卡林和SR 44866的交感抑制作用。5. 我们得出结论,在SHR中,我们研究的两种钾通道开放剂发挥相似的交感抑制作用,对某些血管床的影响大于其他血管床。这些作用不依赖于动脉血压水平,且很可能位于突触前。

相似文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验