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兔膝关节血管的肾上腺素能受体概况

Adrenoceptor profile of blood vessels in the knee joint of the rabbit.

作者信息

Ferrell W R, Khoshbaten A

机构信息

Institute of Physiology, University of Glasgow.

出版信息

J Physiol. 1989 Jul;414:377-83. doi: 10.1113/jphysiol.1989.sp017693.

Abstract
  1. An in vitro preparation of the rabbit knee joint, perfused with oxygenated Locke solution, was used to assess the nature of adrenoceptors within articular blood vessels. 2. Dose/response relationships were obtained to intra-arterial injection of alpha- and beta-adrenoceptor agonists. 3. Adrenaline and noradrenaline produced a similar pattern of increasing constriction of articular vessels with increasing dose of drug. 4. The alpha 1-agonist, phenylephrine, also produced dose-dependent constrictor responses, but the alpha 2-agonist; clonidine, had no effect. The alpha 2-agonist UK-14304 did, however, produce modest vasoconstriction which was not greatly altered by the alpha 1-blocker prazosin. The constrictor effect of noradrenaline was abolished by both the alpha 1,2-blocker phenoxybenzamine and by prazosin but not by the alpha 2-blocker rauwalscine. 5. The beta-adrenoceptor agonist, isoprenaline, had little effect at a dose of 10(-6) M or lower, but gave rise to a constrictor effect at higher concentrations. This response was blocked by phenoxybenzamine but not by the beta 1,2-blocker propranolol, suggesting that the constrictor effect was mediated via alpha-adrenoceptors. 6. The results suggest that alpha 1- and alpha 2-adrenoceptors are present within articular blood vessels, but that beta-receptors are absent. The effects of noradrenaline appear to be mediated principally via alpha 1-adrenoceptors.
摘要
  1. 使用灌注含氧洛克溶液的兔膝关节体外制剂来评估关节血管内肾上腺素能受体的性质。2. 通过动脉内注射α和β肾上腺素能受体激动剂获得剂量/反应关系。3. 肾上腺素和去甲肾上腺素随着药物剂量增加产生类似的关节血管收缩增强模式。4. α1激动剂苯肾上腺素也产生剂量依赖性收缩反应,但α2激动剂可乐定无作用。然而,α2激动剂UK-14304确实产生适度血管收缩,且α1阻滞剂哌唑嗪对此作用影响不大。去甲肾上腺素的收缩作用被α1,2阻滞剂酚苄明和哌唑嗪消除,但未被α2阻滞剂萝芙木碱消除。5. β肾上腺素能受体激动剂异丙肾上腺素在10(-6)M或更低剂量时作用很小,但在较高浓度时产生收缩作用。此反应被酚苄明阻断,但未被β1,2阻滞剂普萘洛尔阻断,提示收缩作用是通过α肾上腺素能受体介导的。6. 结果表明关节血管内存在α1和α2肾上腺素能受体,但不存在β受体。去甲肾上腺素的作用似乎主要通过α1肾上腺素能受体介导。

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