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豚鼠中5-羟色胺依赖的肌阵挛:通过5-羟色胺1A-5-羟色胺2受体相互作用介导

5-HT-dependent myoclonus in guinea pigs: mediation through 5-HT1A-5-HT2 receptor interaction.

作者信息

Eison A S, Wright R N, Freeman R P, Gylys J A

机构信息

CNS Drug Discovery, Bristol-Myers Squibb Company, Wallingford, CT 06492.

出版信息

Brain Res Bull. 1993;30(5-6):687-9. doi: 10.1016/0361-9230(93)90100-p.

Abstract

Investigations utilizing agonists for 5-HT receptor subtypes have been conducted to determine which 5-HT receptor subtype(s) subserve myoclonus in the guinea pig. Administration of a nonselective 5-HT agonist such as 5-MeODMT (5-HT1A/5-HT2 agonist) induces a dose-dependent behavior characterized by head jerking at low doses (1-2 mg/kg, SC) and full-blown myoclonus (continuous rhythmic whole-body jerking) at higher doses (2.5-5 mg/kg, SC). In contrast, the selective 5-HT1A receptor agonist 8-OH-DPAT and the selective 5-HT2 receptor agonist DOI do not induce myoclonus, and elicit only limited head jerking across an otherwise behaviorally active range of doses (1-5 mg/kg, SC). Importantly, the coadministration of both 8-OH-DPAT and DOI results in the emergence of dose-dependent myoclonic behavior. These data suggest that coactivation of 5-HT1A and 5-HT2 receptors may be required for the induction of myoclonus in the guinea pig.

摘要

研究人员利用5-羟色胺(5-HT)受体亚型的激动剂进行了研究,以确定哪种5-HT受体亚型在豚鼠中引起肌阵挛。给予非选择性5-HT激动剂,如5-甲氧基-N,N-二甲基色胺(5-MeODMT,一种5-HT1A/5-HT2激动剂),会诱导出剂量依赖性行为,其特征为低剂量(1-2毫克/千克,皮下注射)时出现头部抽搐,高剂量(2.5-5毫克/千克,皮下注射)时出现全面的肌阵挛(持续有节奏的全身抽搐)。相比之下,选择性5-HT1A受体激动剂8-羟基二丙胺基四氢萘(8-OH-DPAT)和选择性5-HT2受体激动剂1,2-二甲基-4,5-亚甲基二氧基苯丙胺(DOI)不会诱导肌阵挛,并且在整个行为活跃的剂量范围内(1-5毫克/千克,皮下注射)仅引起有限的头部抽搐。重要的是,同时给予8-OH-DPAT和DOI会导致剂量依赖性肌阵挛行为的出现。这些数据表明,5-HT1A和5-HT2受体的共同激活可能是豚鼠诱导肌阵挛所必需的。

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