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偏侧帕金森病猴的多巴胺能机制

Dopaminergic mechanisms in hemiparkinsonian monkeys.

作者信息

Barone P, Bankiewicz K S, Corsini G U, Kopin I J, Chase T N

机构信息

Experimental Therapeutics Branch, National Institute of Neurological and Communicative Disorders and Stroke, Bethesda, MD 20892.

出版信息

Neurology. 1987 Oct;37(10):1592-5. doi: 10.1212/wnl.37.10.1592.

Abstract

The motor effects of direct agonists which act selectively on certain dopamine receptors were studied in monkeys rendered hemiparkinsonian by unilateral intracarotid injection of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). The D-2 dopamine agonist, LY 171555, but not the D-1 agonist, SKF 38393, reduced parkinsonian signs and induced rotation away from the side of the nigral lesion. When administered together, SKF 38393 diminished the LY 171555-induced turning in a dose-dependent manner. A selective D-1 antagonist, SCH 23390, induced mild and brief rotation when administered alone. These results suggest that D-2 receptor stimulation is necessary to ameliorate parkinsonism, but that pharmacologic manipulation of both D-1 and D-2 receptors may be required for an optimal therapeutic response.

摘要

在通过单侧颈内注射1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)而导致偏侧帕金森病的猴子中,研究了选择性作用于某些多巴胺受体的直接激动剂的运动效应。D-2多巴胺激动剂LY 171555可减轻帕金森病症状并诱导动物向远离黑质损伤侧旋转,而D-1激动剂SKF 38393则无此作用。当同时给药时,SKF 38393以剂量依赖方式减弱LY 171555诱导的旋转。选择性D-1拮抗剂SCH 23390单独给药时可诱导轻微且短暂的旋转。这些结果表明,刺激D-2受体对于改善帕金森病是必要的,但要获得最佳治疗反应可能需要对D-1和D-2受体进行药物调控。

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