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γ-氨基丁酸对脊髓麻醉犬心脏交感神经节中血管紧张素II兴奋作用的拮抗作用。

Antagonism by gamma-aminobutyric acid of the stimulant effect of angiotensin II on cardiac sympathetic ganglia in spinal dogs.

作者信息

Furukawa T, Kushiku K

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):149-53. doi: 10.1007/BF00500071.

Abstract

The effects of angiotensin II and neuro-aminoacids administered through the right subclavian artery (i.a.) to the cardiac sympathetic ganglia were investigated in spinal dogs. Angiotensin II (1--8 micrograms) elicited a dose-dependent positive chronotropic effect which was reduced after i.a. injection of saralasin (100 micrograms). The effect of angiotensin II was not reduced after combined treatment with either hexamethonium (10 mg/kg) plus atropine (0.1 mg/kg) or hemicholinium-3 (5 mg/kg) plus preganglionic stimulation. The dose-dependent response to angiotensin II of heart rate was inhibited by GABA (50, 500 micrograms), GABOB (500 micrograms) and muscimol (50, 100 micrograms). The inhibition of the response to angiotensin II by a small dose of GABA (50 micrograms), but not by a high one (500 micrograms), was antagonized by i.a. injection of picrotoxin (2 mg). The positive chronotropism induced by bethanechol (25, 50 micrograms) and a small dose of acetylcholine (25 micrograms) were significantly inhibited by a high dose (500 micrograms) but not by a low dose (50 micrograms) of GABA. These results confirm that angiotensin II stimulates cardiac chronotropism by acting on the angiotensin II receptor located at the cardiac ganglia and show that this stimulant effect is antagonized by GABA.

摘要

在脊髓犬中研究了经右锁骨下动脉(动脉内)给予心脏交感神经节的血管紧张素II和神经氨基酸的作用。血管紧张素II(1 - 8微克)引起剂量依赖性的正性变时效应,在动脉内注射沙拉新(100微克)后该效应减弱。在与六甲铵(10毫克/千克)加阿托品(0.1毫克/千克)或半胱氨酸-3(5毫克/千克)联合治疗并加上节前刺激后,血管紧张素II的作用并未减弱。GABA(50、500微克)、GABOB(500微克)和蝇蕈醇(50、100微克)抑制了心率对血管紧张素II的剂量依赖性反应。小剂量GABA(50微克)而非大剂量(500微克)对血管紧张素II反应的抑制作用,被动脉内注射苦味毒(2毫克)拮抗。氨甲酰甲胆碱(25、50微克)和小剂量乙酰胆碱(25微克)诱导的正性变时作用,被高剂量(500微克)而非低剂量(50微克)的GABA显著抑制。这些结果证实血管紧张素II通过作用于位于心脏神经节的血管紧张素II受体刺激心脏变时作用,并表明这种刺激作用被GABA拮抗。

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