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组胺在觉醒和认知调节中的作用:人脑组胺H1受体的功能神经影像学研究

Roles of histamine in regulation of arousal and cognition: functional neuroimaging of histamine H1 receptors in human brain.

作者信息

Tashiro Manabu, Mochizuki Hideki, Iwabuchi Kentaro, Sakurada Yumiko, Itoh Masatoshi, Watanabe Takehiko, Yanai Kazuhiko

机构信息

Department of Pharmacology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Miyagi, 980-8575, Sendai-shi, Japan.

出版信息

Life Sci. 2002 Dec 20;72(4-5):409-14. doi: 10.1016/s0024-3205(02)02276-2.

Abstract

Brain histamine is involved in a wide range of physiological functions such as regulation of the sleep-wake cycle, arousal, cognition, and memory mainly through interactions with histamine H1 receptors (H1Rs). Neurons producing histamine, histaminergic neurons, are exclusively located in the posterior hypothalamus and transmit histamine to almost all regions of the brain. Histamine H1 antagonists, or antihistamines, often prescribed for treatment of allergic disorders, sometimes induce sleepiness and cognitive deficits. It is understood that the mechanism of such CNS side effects is that antihistamine blocks H1Rs in the brain. The purpose of the present study was to compare the CNS side effects of different antihistamines. Subjective sleepiness was measured using the Stanford Sleepiness Scale (SSS) and psychomotor performance was examined by a tachistoscope testing system in healthy, young, Japanese volunteers (16 males, 20-28 yrs.) before and after oral administration of antihistamines such as fexofenadine (FEX) and cetirizine (CET). Additionally, H1R occupancy by antihistamines was examined by PET with 11C-doxepin in 8 volunteers. The results of SSS and psychomotor tests demonstrated that FEX tended to be less sedative than CET though the difference was not statistically significant. PET measurements revealed that no H1Rs in the cerebral cortex were occupied by FEX while about 30% of H1Rs were occupied by CET. In summary, it was confirmed that histamine and H1Rs are involved in maintaining arousal and cognition in humans, and that the severity of clinical symptoms is correlated to the amount of antihistamine that penetrated into the brain.

摘要

脑内组胺主要通过与组胺H1受体(H1Rs)相互作用,参与广泛的生理功能,如调节睡眠 - 觉醒周期、唤醒、认知和记忆。产生组胺的神经元,即组胺能神经元,仅位于下丘脑后部,并将组胺传递至大脑的几乎所有区域。常用于治疗过敏性疾病的组胺H1拮抗剂,即抗组胺药,有时会引起嗜睡和认知缺陷。据了解,这种中枢神经系统副作用的机制是抗组胺药阻断了脑内的H1Rs。本研究的目的是比较不同抗组胺药的中枢神经系统副作用。在健康、年轻的日本志愿者(16名男性,20 - 28岁)口服抗组胺药如非索非那定(FEX)和西替利嗪(CET)之前和之后,使用斯坦福嗜睡量表(SSS)测量主观嗜睡程度,并通过速示仪测试系统检测精神运动表现。此外,在8名志愿者中通过PET使用11C - 多塞平检测抗组胺药对H1R的占有率。SSS和精神运动测试结果表明,虽然差异无统计学意义,但FEX的镇静作用往往比CET小。PET测量显示,FEX未占据大脑皮层中的H1Rs,而CET占据了约30%的H1Rs。总之,证实了组胺和H1Rs参与维持人类的觉醒和认知,并且临床症状的严重程度与渗透到脑内的抗组胺药的量相关。

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