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纳洛酮和纳曲酮对促甲状腺激素释放激素诱导的家兔结肠转运刺激的阻断作用。

Blockade by naloxone and naltrexone of the TRH-induced stimulation of colonic transit in the rabbit.

作者信息

Horita A, Carino M A, Pae Y S

出版信息

Eur J Pharmacol. 1985 Feb 5;108(3):289-93. doi: 10.1016/0014-2999(85)90451-0.

Abstract

Thyrotropin releasing hormone (TRH), administered intracerebroventricularly (i.c.v.) in microgram quantities to anesthetized rabbits, produces marked stimulation of colonic motility, transit, fluid accumulation, and accompanied by a portal hyperserotonemia. In this study we found that pretreatment of rabbits with naloxone (2.5 mg/kg) or naltrexone (1.0 mg/kg) attenuated or blocked the TRH-induced colonic transit and increase in luminal fluid, but not the hypermotility nor the hyperserotonemia. In this respect the narcotic antagonist effects resemble those produced by the antiserotonin compounds or opiate agonists.

摘要

向麻醉的兔子脑室内注射微克量的促甲状腺激素释放激素(TRH),可显著刺激结肠运动、运输、液体蓄积,并伴有门静脉高血清素血症。在本研究中,我们发现用纳洛酮(2.5毫克/千克)或纳曲酮(1.0毫克/千克)预处理兔子可减弱或阻断TRH诱导的结肠运输及管腔内液体增加,但不能减弱或阻断结肠运动亢进或高血清素血症。在这方面,麻醉拮抗剂的作用类似于抗血清素化合物或阿片类激动剂产生的作用。

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