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H1组胺受体阻滞剂氯苯那敏可完全阻止大鼠因固定应激诱导的快速眼动睡眠增加。

The H1 histamine receptor blocker, chlorpheniramine, completely prevents the increase in REM sleep induced by immobilization stress in rats.

作者信息

Rojas-Zamorano J A, Esqueda-Leon E, Jimenez-Anguiano A, Cintra-McGlone L, Mendoza Melendez M A, Velazquez Moctezuma J

机构信息

Department of Biology of Reproduction, Universidad Autonoma Metropolitana-Iztapalapa, CP 09340, Mexico City, Mexico.

出版信息

Pharmacol Biochem Behav. 2009 Jan;91(3):291-4. doi: 10.1016/j.pbb.2008.07.011. Epub 2008 Jul 22.

Abstract

Chlorpheniramine is a selective antagonist of the H1 histaminergic receptor subtype and its effects in humans include somnolence. Chlorpheniramine affects sleep in rats, mainly by decreasing REM sleep. On the other hand, stress by immobilization induces an important increase in the percentage of REM sleep. In this study we analyzed the effects of blocking histaminergic receptors on REM sleep induced by immobilization stress. Adult male Wistar rats were chronically implanted for sleep recording. Immobilization stress was induced by placing the rat in a small cylinder for 2 h. Experimental conditions were: A. Control; B. Stress; C. Stress plus vehicle and D. Stress plus chlorpheniramine. Independent experiments were done both in the dark, as well as the light period. Results showed that the increase in REM sleep observed after immobilization stress was completely abolished by chlorpheniramine, both in the dark and in the light phase. Furthermore, the decrease in REM sleep was significant even when compared to the non-stressed control rats. REM sleep latency was also significantly longer during both light phases. The present results suggest that REM sleep is quite sensitive to histaminergic blockage. It is possible that chlorpheniramine is also blocking the cholinergic mechanisms generating REM sleep.

摘要

氯苯那敏是H1组胺能受体亚型的选择性拮抗剂,其对人类的影响包括嗜睡。氯苯那敏影响大鼠睡眠,主要是通过减少快速眼动睡眠。另一方面,固定应激会导致快速眼动睡眠百分比显著增加。在本研究中,我们分析了阻断组胺能受体对固定应激诱导的快速眼动睡眠的影响。成年雄性Wistar大鼠被长期植入用于睡眠记录。通过将大鼠置于小圆柱体中2小时来诱导固定应激。实验条件为:A.对照;B.应激;C.应激加赋形剂;D.应激加氯苯那敏。在黑暗期和光照期都进行了独立实验。结果表明,氯苯那敏在黑暗期和光照期均完全消除了固定应激后观察到的快速眼动睡眠增加。此外,即使与非应激对照大鼠相比,快速眼动睡眠的减少也很显著。在两个光照期,快速眼动睡眠潜伏期也显著延长。目前的结果表明,快速眼动睡眠对组胺能阻断相当敏感。氯苯那敏也有可能阻断了产生快速眼动睡眠的胆碱能机制。

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