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血清素受体拮抗剂的高血糖特性。

Hyperglycemic properties of serotonin receptor antagonists.

作者信息

Wozniak K M, Linnoila M

机构信息

Laboratory of Clinical Studies, National Institute on Alcohol Abuse & Alcoholism, DICBR, Bethesda, MD 20892.

出版信息

Life Sci. 1991;49(2):101-9. doi: 10.1016/0024-3205(91)90023-5.

Abstract

Several serotonin (5-HT) receptor antagonists with varying specificities for the 5-HT receptor types, were studied with regard to their effects on blood glucose levels in mice. The non-selective antagonists, metergoline and methysergide, proved to be hyperglycemic at doses commonly used to antagonize 5-HT receptors. In contrast, ritanserin (a 5-HT2 and 5-HT1c antagonist) and MDL 72222 (a 5-HT3 antagonist) were effective only at doses which surpassed the dose range considered to be selective for their respective receptors. The results suggest that 5-HT systems play a role in maintaining glucose homeostasis and that 5-HT1 receptors may be particularly important in this function. Furthermore, the inherent hyperglycemic properties of non-selective serotonin antagonists described here, are pertinent to studies using these agents to investigate glucose metabolism.

摘要

研究了几种对5-羟色胺(5-HT)受体类型具有不同特异性的5-HT受体拮抗剂对小鼠血糖水平的影响。非选择性拮抗剂麦角苄酯和甲基麦角新碱在通常用于拮抗5-HT受体的剂量下被证明会导致血糖升高。相比之下,利坦色林(一种5-HT2和5-HT1c拮抗剂)和MDL 72222(一种5-HT3拮抗剂)仅在超过被认为对其各自受体具有选择性的剂量范围内才有效。结果表明,5-HT系统在维持葡萄糖稳态中起作用,并且5-HT1受体在该功能中可能特别重要。此外,此处描述的非选择性血清素拮抗剂固有的高血糖特性与使用这些药物研究葡萄糖代谢的研究相关。

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