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α-1肾上腺素能受体介导的血管平滑肌收缩脱敏。

Desensitization of alpha-1 adrenergic receptor-mediated vascular smooth muscle contraction.

作者信息

Lurie K G, Tsujimoto G, Hoffman B B

出版信息

J Pharmacol Exp Ther. 1985 Jul;234(1):147-52.

PMID:2989501
Abstract

Desensitization of alpha-1 receptor-mediated smooth muscle contraction was studied in rabbit aorta. Incubation of rabbit aorta ring segments with epinephrine (10(-6) M) for 7 hr resulted in a 10-fold loss in sensitivity of the tissue to alpha-1 adrenergic receptor-mediated contraction with no change in maximal force of contraction. This loss in sensitivity was specific for alpha-1 receptor-mediated contraction because responses to histamine and serotonin were unchanged in these aortas. Conversely, prolonged exposure of vessels to histamine (10(-5) M) led to desensitization of histamine-mediated contraction without altering responses to alpha-1 receptor stimulation. Using [125I] BE2254, a potent alpha-1 receptor antagonist, the loss in sensitivity to catecholamines was found not to be mediated by down-regulation of alpha-1 receptors nor by a loss in their affinity for epinephrine. However, desensitization was associated with a blunting of alpha-1 receptor stimulation of phosphatidylinositol turnover. These results suggest that desensitization of alpha-1 receptor-mediated contraction in rabbit aorta does not appear to be mediated by changes in receptor number or affinity but may involve alterations in receptor coupling.

摘要

在兔主动脉中研究了α-1受体介导的平滑肌收缩脱敏现象。将兔主动脉环段与肾上腺素(10⁻⁶ M)孵育7小时,导致组织对α-1肾上腺素能受体介导的收缩敏感性降低10倍,而最大收缩力无变化。这种敏感性降低对α-1受体介导的收缩具有特异性,因为这些主动脉对组胺和5-羟色胺的反应未改变。相反,血管长时间暴露于组胺(10⁻⁵ M)导致组胺介导的收缩脱敏,而不改变对α-1受体刺激的反应。使用强效α-1受体拮抗剂[¹²⁵I]BE2254,发现对儿茶酚胺敏感性的降低不是由α-1受体下调介导的,也不是由其对肾上腺素亲和力的丧失介导的。然而,脱敏与α-1受体刺激磷脂酰肌醇周转的减弱有关。这些结果表明,兔主动脉中α-1受体介导的收缩脱敏似乎不是由受体数量或亲和力的变化介导的,而是可能涉及受体偶联的改变。

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