Suppr超能文献

去大脑大鼠中5-羟色胺诱发心动过速的机制研究

Study on the mechanism of 5-HT-induced tachycardia in the pithed rat.

作者信息

Midol-Monnet M, Heimburger M, Davy M, Beslot F, Cohen Y

机构信息

Laboratoire de Pharmacologie, U.A.-C.N.R.S. 594, Faculté de Pharmacie, Chatenay-Malabry, France.

出版信息

Gen Pharmacol. 1989;20(6):755-8. doi: 10.1016/0306-3623(89)90324-8.

Abstract
  1. Intravenous infusion of serotonin (5-HT) (2.5, 5, 10 and 20 micrograms/kg/min) in pithed rats induced a dose-dependent sustained tachycardia. 2. Pretreatment by phentolamine or diltiazem did not modify the chronotropic response to 5-HT. In contrast, atenolol antagonized this tachycardia and the 5-HT antagonists methysergide, ketanserin and MDL 72222 reduced it. 3. The 5-HT-induced tachycardia was abolished by desipramine and was not affected by fluvoxamine, a specific 5-HT uptake inhibitor. Surrenalectomy did not change the response to 5-HT but catecholamine depletion by reserpine markedly inhibited it. 4. Infusion of 5-HT increased the ratio of noradrenaline (NA) in the heart to NA in plasma, from 1.70 in control group to 2.76 in treated group (P less than 0.05). Desipramine inhibited this effect. 5. It was concluded that the tachycardia induced by an infusion of 5-HT in pithed rat results from a complex mechanism involving mainly the release of NA from the cardiac sympathetic nerves and a less important direct 5-HT2 mechanism.
摘要
  1. 向脊髓损毁大鼠静脉输注5-羟色胺(5-HT)(2.5、5、10和20微克/千克/分钟)可诱发剂量依赖性的持续性心动过速。2. 用酚妥拉明或地尔硫䓬预处理并未改变对5-HT的变时反应。相比之下,阿替洛尔可拮抗这种心动过速,5-HT拮抗剂美西麦角、酮色林和MDL 72222可使其减慢。3. 5-HT诱发的心动过速可被地昔帕明消除,且不受特异性5-HT摄取抑制剂氟伏沙明的影响。肾上腺切除并未改变对5-HT的反应,但利血平使儿茶酚胺耗竭可显著抑制该反应。4. 输注5-HT可使心脏中去甲肾上腺素(NA)与血浆中NA的比值从对照组的1.70增加至处理组的2.76(P<0.05)。地昔帕明可抑制这种作用。5. 得出的结论是,向脊髓损毁大鼠输注5-HT所诱发的心动过速是由一种复杂机制引起的,该机制主要涉及心脏交感神经释放NA以及不太重要的直接5-HT2机制。

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