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[布他拉莫尔对映体对大鼠脑下丘脑酪氨酸羟化酶的影响]

[Effect of butaclamol enantiomers on hypothalamic tyrosine hydroxylase in the rat brain].

作者信息

Mineeva M F, Raevskiĭ K S

出版信息

Biull Eksp Biol Med. 1984 Oct;98(10):453-6.

PMID:6208950
Abstract

The authors demonstrate stereospecificity of the action of butaclamol enantiomers on substrate inhibition of hypothalamic tyrosine hydroxylase (TH) and regulation of the tyrosine hydroxylase response by the presynaptic membrane (presynaptic receptors) of rat hypothalamus synaptosomes under membrane activation with dopamine. The effect of (+)-butaclamol on the substrate inhibition of TH was noticeable at a concentration of 10(-8)M, reaching a maximum at 10(-5)M. (-)-Butaclamol administered at the same concentrations did not influence the substrate inhibition of the enzyme. (+)-Butaclamol added to the incubation medium containing hypothalamic synaptosomes concurrently with dopamine (10(-5)M) completely blocked the regulatory action of the latter on TH, with this action mediated via presynaptic receptors. (-)-Butaclamol (10(-5)M) antagonized the action of dopamine under the same conditions. The data obtained indicate high stereo-specificity of butaclamol enantiomers as regards their effect on presynaptic regulation of TH, suggesting that elimination of the substrate inhibition of hypothalamic TH is a stereoselective effect of neuroleptics and can be a prognostically important criterion in the appraisal of compounds with potential neuroleptic activity.

摘要

作者证明了布他拉莫尔对映体作用于下丘脑酪氨酸羟化酶(TH)底物抑制以及在多巴胺激活膜的情况下对大鼠下丘脑突触体突触前膜(突触前受体)调节酪氨酸羟化酶反应的立体特异性。(+)-布他拉莫尔在浓度为10^(-8)M时对TH底物抑制的作用就很明显,在10^(-5)M时达到最大值。以相同浓度给予的(-)-布他拉莫尔对该酶的底物抑制没有影响。与多巴胺(10^(-5)M)同时添加到含有下丘脑突触体的孵育培养基中的(+)-布他拉莫尔完全阻断了后者对TH的调节作用,这种作用是通过突触前受体介导的。在相同条件下,(-)-布他拉莫尔(10^(-5)M)拮抗多巴胺的作用。所获得的数据表明布他拉莫尔对映体在其对TH突触前调节的作用方面具有高度立体特异性,这表明消除下丘脑TH的底物抑制是抗精神病药物的一种立体选择性作用,并且可能是评估具有潜在抗精神病活性化合物的一个具有预后重要性的标准。

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