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使用酚苄明区分外周和中枢神经激肽受体。

A differentiation between peripheral and central neurokinin receptors using phenoxybenzamine.

作者信息

Vaught J L, Scott R W, Jacoby H I

出版信息

Eur J Pharmacol. 1986 Jun 24;125(3):325-31. doi: 10.1016/0014-2999(86)90788-0.

Abstract

Concentrations of phenoxybenzamine ranging from 0.33-33 micron produced a competitive block of kassinin-, neurokinin A- and neurokinin B-induced contractions of the guinea-pig ileum with pA2 values of 6.6, 5.6 and 6.2, respectively. Physalaemin- and substance P-induced contractions were insensitive to phenoxybenzamine treatment. Differences in sensitivity to phenoxybenzamine and pA2 values suggest the existence of at least two and possibly three neurokinin receptors in the guinea-pig ileum. Injected intrathecally to mice, phenoxybenzamine blocked neurokinin-induced, but not bombesin- or somatostatin-induced, reciprocal hind limb scratching. Phenozybenzamine was 6-32 times more effective in blocking neurokinin B-induced scratching than substance P, kassinin, physalaemin or neurokinin A-induced scratching. These results suggest that multiple peripheral and central neurokinin receptors can be differentiated from one another by phenoxybenzamine treatment. They also suggest the existence of a distinct neurokinin B receptor in the mouse spinal cord and the apparent identification of a third neurokinin receptor in the guinea-pig ileum.

摘要

苯氧苄胺浓度在0.33 - 33微摩尔范围内,可竞争性阻断卡辛宁、神经激肽A和神经激肽B诱导的豚鼠回肠收缩,其pA2值分别为6.6、5.6和6.2。促胰液素和P物质诱导的收缩对苯氧苄胺处理不敏感。对苯氧苄胺敏感性和pA2值的差异表明豚鼠回肠中至少存在两种,可能三种神经激肽受体。鞘内注射到小鼠体内时,苯氧苄胺可阻断神经激肽诱导的,但不阻断蛙皮素或生长抑素诱导的后肢交替抓挠。苯氧苄胺阻断神经激肽B诱导的抓挠比阻断P物质、卡辛宁、促胰液素或神经激肽A诱导的抓挠有效6 - 32倍。这些结果表明,通过苯氧苄胺处理可区分多种外周和中枢神经激肽受体。它们还表明小鼠脊髓中存在一种独特的神经激肽B受体,并且在豚鼠回肠中明显鉴定出第三种神经激肽受体。

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