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氨基葡萄糖诱导的摄食抑制受大鼠下丘脑神经元组胺调控。

Aminoglucose-induced feeding suppression is regulated by hypothalamic neuronal histamine in rats.

作者信息

Kang M, Yoshimatsu H, Kurokawa M, Oohara A, Sakata T

机构信息

Department of Internal Medicine I, School of Medicine, Oita Medical University, Japan.

出版信息

Brain Res. 1993 Dec 24;631(2):181-6. doi: 10.1016/0006-8993(93)91533-x.

Abstract

Central mechanisms involved in feeding suppression produced by 1-deoxy-D-glucosamine (1-DGlcN) and 1-deoxy-N-acetylglucosamine (1-DGlcNAc) are unclear. To clarify the mechanisms, we investigated the role of hypothalamic neuronal histamine (HA) in feeding suppression induced by 1-DGlcN and 1-DGlcNAc in rats. Food intake was suppressed for 3 days after a single infusion of 24 mumol 1-DGlcN into the third cerebroventricle (i.c.v.). Depletion of presynaptic HA due to intraperitoneal infusion (i.p.) of alpha-fluoromethylhistidine (FMH), a specific inhibitor of the HA synthesizing enzyme histidine decarboxylase (HDC), abolished feeding suppression completely. Blockade of postsynaptic H1-receptors by i.p. injection of 26 mumol chlorpheniramine also abolished the suppression. Oral administration of 2.4 mmol 1-DGlcNAc suppressed food intake. However, depletion of neuronal HA due to FMH did not affect the suppression. I.c.v. infusion of 24 mumol 1-DGlcN increased turnover rate of HA at 1 h after the infusion. Hypothalamic HA concentration, but not that of tele-methylhistamine (t-MH), increased at 24 h after i.c.v. infusion of 1-DGlcN, which suggests a correlation between HA concentration and the behavioral response. These results indicate that 1-DGlcN, but not 1-DGlcNAc, modulates feeding suppression through HA neurons in the hypothalamus. Differences in mechanisms of feeding suppression by these aminoglucoses may depend on the principal sites of action in the brain and/or peripheral organs.

摘要

1-脱氧-D-葡萄糖胺(1-DGlcN)和1-脱氧-N-乙酰葡萄糖胺(1-DGlcNAc)产生摄食抑制作用的中枢机制尚不清楚。为了阐明这些机制,我们研究了下丘脑神经元组胺(HA)在1-DGlcN和1-DGlcNAc诱导的大鼠摄食抑制中的作用。向第三脑室(i.c.v.)单次注入24 μmol 1-DGlcN后,食物摄入量被抑制了3天。腹腔注射(i.p.)α-氟甲基组胺(FMH),一种组胺合成酶组氨酸脱羧酶(HDC)的特异性抑制剂,导致突触前HA耗竭,完全消除了摄食抑制。腹腔注射26 μmol氯苯那敏阻断突触后H1受体也消除了这种抑制作用。口服2.4 mmol 1-DGlcNAc可抑制食物摄入。然而,FMH导致的神经元HA耗竭并未影响这种抑制作用。向第三脑室注入24 μmol 1-DGlcN后1小时,HA的周转率增加。向第三脑室注入1-DGlcN后24小时,下丘脑HA浓度升高,但甲基组胺(t-MH)浓度未升高,这表明HA浓度与行为反应之间存在相关性。这些结果表明,1-DGlcN而非1-DGlcNAc通过下丘脑的HA神经元调节摄食抑制。这些氨基葡萄糖在摄食抑制机制上的差异可能取决于它们在大脑和/或外周器官中的主要作用部位。

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