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硝苯地平对交感神经血管收缩的抑制作用:血管α2-肾上腺素能受体的作用

Attenuation of sympathetic vasoconstriction by nifedipine: the role of vascular alpha 2-adrenoceptors.

作者信息

Saeed M, Holtz J, Elsner D, Bassenge E

出版信息

Eur J Pharmacol. 1983 Oct 14;94(1-2):149-53. doi: 10.1016/0014-2999(83)90453-3.

Abstract

The effects of nifedipine on hindlimb vasoconstriction caused by norepinephrine infusion and sympathetic stimulation (0.1-1.0 Hz) were compared in dogs given 0.12 mg/kg prazosin or 0.3 mg/kg rauwolscine. Constrictions due to stimulation or norephinephrine with prazosin, presumed to be mediated by vascular alpha 2-adrenoceptors, were significantly attenuated by 30 micrograms/kg nifedipine, while constrictions with rauwolscine, presumably alpha 1-mediated, remained unaffected. These data support the hypothesis that the antihypertensive effect of calcium antagonists is based upon interference with alpha 2-mediated sympathetic vasoconstriction.

摘要

在给予0.12mg/kg哌唑嗪或0.3mg/kg萝芙木碱的犬中,比较了硝苯地平对去甲肾上腺素输注和交感神经刺激(0.1 - 1.0Hz)引起的后肢血管收缩的影响。用哌唑嗪时,由刺激或去甲肾上腺素引起的血管收缩,推测是由血管α2 - 肾上腺素能受体介导的,可被30μg/kg硝苯地平显著减弱,而用萝芙木碱时,推测是由α1介导的血管收缩则不受影响。这些数据支持了钙拮抗剂的降压作用是基于干扰α2介导的交感神经血管收缩这一假说。

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