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氯丙嗪对鸡脑唾液酸掺入神经节苷脂和糖蛋白的影响(作者译)

[Effect of chlorpromazine on the incorporation of sialic acid into gangliosides and glycoproteins of the chicken brain (author's transl)].

作者信息

Rösner H

出版信息

Psychopharmacology (Berl). 1976 Jul 9;48(1):25-9. doi: 10.1007/BF00423302.

Abstract

Three-days-old White Leghorn chickens were used to study the effect of i.p.-injected chlorpromazine (CP, 2.5 or 5 mg/animal) on the incorporation of N-(3H)-acetylmannosamine into glycoprotein- and ganglioside-bound sialic acid and 14C-histidine into the proteins of the cerebrum, the optic lobes, and the cerebellum after incorporation periods of 1-24 h. All experiments were performed under constant temperature conditions. 1. The incorporation of 14C-histidine into the proteins of the optic lobes was not influenced by CP. 2. Within 24 h in the optic lobes neither the concentration of particle-bound sialic acid (mug sialic acid/mg protein) nor the content of radioactive-labeled sialic acid precursor was affected by the drug. 3. The rate of incorporation of labeled sialic acid into glycoproteins and gangliosides, however, was up to 6 h after the injection of the precursor much lower in the CP-treated animals than in controls. This may indicate, that the turnover of sialo-compounds was diminished by CP. 4. The inhibition was the most intensive in the cerebrum (up to 80%), lower in the optic lobes (up to 70%), and only small in the cerebellum (up to 20%), but was always the same for glycoproteins and gangliosides. The different inhibition rates in the different structures may indicate a correlation between the pharmacologic, sedative effects of the drug and the diminished turnover of sialo compounds.

摘要

使用3日龄的白来航鸡研究腹腔注射氯丙嗪(CP,2.5或5mg/只动物)对N-(3H)-乙酰甘露糖胺掺入糖蛋白和神经节苷脂结合唾液酸以及14C-组氨酸在1-24小时掺入大脑、视叶和小脑蛋白质中的影响。所有实验均在恒温条件下进行。1. 14C-组氨酸掺入视叶蛋白质不受CP影响。2. 在视叶中,24小时内药物既不影响颗粒结合唾液酸(微克唾液酸/毫克蛋白质)的浓度,也不影响放射性标记唾液酸前体的含量。3. 然而,在前体注射后长达6小时,CP处理动物中标记唾液酸掺入糖蛋白和神经节苷脂的速率比对照组低得多。这可能表明CP降低了唾液酸化合物的周转。4. 抑制作用在大脑中最为强烈(高达80%),在视叶中较低(高达70%),在小脑中仅轻微(高达20%),但对糖蛋白和神经节苷脂始终相同。不同结构中不同的抑制率可能表明该药物的药理镇静作用与唾液酸化合物周转减少之间存在相关性。

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