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重新审视小鼠大脑软脑膜小动脉反应。

Pial arteriolar responses in the mouse brain revisited.

作者信息

Rosenblum W I

出版信息

Stroke. 1976 May-Jun;7(3):283-7. doi: 10.1161/01.str.7.3.283.

Abstract

Arteriolar responses were measured on the cerebral surface of the mouse using an image splitter and TV monitor. The response to locally applied norepinephrine (NOR) was significantly more frequent for vessels greater than 30 mu I.D. than for smaller vessels. However, even the smaller vessels were frequently constricted by NOR in doses of 5 mug per milliliter. Reserpine (5 mg per kilogram) failed to alter the response to NOR at either 24 or 72 hours after reserpinization. At 48 hours the threshold dose of NOR was reduced, but the effect was slight (two-tailed, P = 0.08). Both propranolol (10(-6) M3 and phentolamine (10(-5M) blocked responses to 5 mug per milliliter of NOR, but neither agent altered resting arteriolar diameter. Isoproterenol, tyramine, and histamine had no effect. Serotonin (5HT) constricted the arterioles but did not potentiate the response to NOR. Additive or potentiated effects were not observed with NOR 5HT or histamine in any combination. These data indicate the presence of alpha-adrenergic receptors in murine cerebral surface arterioles, but do not establish a significant tonic effect of norepinephrine. The existence or role of a beta-receptor in these murine cerebral surface arterioles remains an unsettled question.

摘要

使用图像分割器和电视监视器在小鼠脑表面测量小动脉反应。大于30微米内径的血管对局部应用去甲肾上腺素(NOR)的反应比小血管更频繁。然而,即使是小血管也经常被每毫升5微克剂量的NOR收缩。利血平(每千克5毫克)在利血平化后24小时或72小时均未改变对NOR的反应。在48小时时,NOR的阈值剂量降低,但效果轻微(双侧,P = 0.08)。普萘洛尔(10^(-6) M)和酚妥拉明(10^(-5) M)均阻断了对每毫升5微克NOR的反应,但两种药物均未改变小动脉的静息直径。异丙肾上腺素、酪胺和组胺无作用。5-羟色胺(5HT)使小动脉收缩,但不增强对NOR的反应。NOR与5HT或组胺的任何组合均未观察到相加或增强作用。这些数据表明小鼠脑表面小动脉存在α-肾上腺素能受体,但未证实去甲肾上腺素具有显著的张力作用。这些小鼠脑表面小动脉中β-受体的存在或作用仍然是一个未解决的问题。

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