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血清素诱导的犬肾血管收缩。

Serotonin-induced vasoconstriction in dog kidney.

作者信息

Takahashi T, Hisa H, Satoh S

机构信息

Department of Pharmacology, Tohoku University, Sendai, Japan.

出版信息

J Cardiovasc Pharmacol. 1992;20(5):779-84.

PMID:1280741
Abstract

Serotonin (5-HT 0.1 and 0.3 micrograms/kg) was injected as a bolus into the renal artery of anesthetized dogs. Renal blood flow (RBF) decreased initially after 5-HT injection and then increased. The 5-HT-induced decrease in RBF was potentiated during intrarenal infusion of a 5-HT1 and 5-HT2 antagonist methysergide at 3 micrograms/kg/min or of a 5-HT2 antagonist ketanserin (3-30 micrograms/kg/min), but methysergide at 30 micrograms/kg/min attenuated the decrease in RBF. The delayed increase in RBF was suppressed during ketanserin or methysergide infusion. In ketanserin-pretreated dogs, methysergide (3-30 micrograms/kg/min) dose-dependently suppressed the 5-HT-induced decrease in RBF. A 5-HT3 antagonist, ICS 205-930 (3-30 micrograms/kg/min), did not affect the 5-HT-induced RBF responses. A Ca2+ entry blocker CD-349 (30 and 100 ng/kg/min) and a Ca2+ release inhibitor TMB-8 (30 and 100 micrograms/kg/min) suppressed the 5-HT-induced decrease in RBF. These results suggest that 5-HT activates 5-HT1 receptors to induce vasoconstriction by mobilization of extracellular and intracellular Ca2+, but simultaneous activation of 5-HT2 receptors attenuates the vasoconstriction, probably by causing vasodilation in dog kidney.

摘要

将血清素(5-羟色胺,0.1和0.3微克/千克)以大剂量注射到麻醉犬的肾动脉中。注射5-羟色胺后,肾血流量(RBF)起初下降,随后上升。在肾内以3微克/千克/分钟的速度输注5-羟色胺1和5-羟色胺2拮抗剂美西麦角或5-羟色胺2拮抗剂酮色林(3 - 30微克/千克/分钟)时,5-羟色胺诱导的肾血流量下降增强,但30微克/千克/分钟的美西麦角可减弱肾血流量的下降。在输注酮色林或美西麦角期间,肾血流量的延迟增加受到抑制。在预先用酮色林处理的犬中,美西麦角(3 - 30微克/千克/分钟)剂量依赖性地抑制5-羟色胺诱导的肾血流量下降。5-羟色胺3拮抗剂ICS 205 - 930(3 - 30微克/千克/分钟)不影响5-羟色胺诱导的肾血流量反应。钙离子内流阻滞剂CD - 349(30和100纳克/千克/分钟)和钙离子释放抑制剂TMB - 8(30和100微克/千克/分钟)抑制5-羟色胺诱导的肾血流量下降。这些结果表明,5-羟色胺激活5-羟色胺1受体,通过动员细胞外和细胞内钙离子来诱导血管收缩,但5-羟色胺2受体的同时激活可能通过引起犬肾血管舒张来减弱血管收缩。

相似文献

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Serotonin-induced renin release in the dog kidney.血清素诱导犬肾素释放
Eur J Pharmacol. 1991 Feb 14;193(3):315-20. doi: 10.1016/0014-2999(91)90145-g.

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