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大鼠脑内的胆囊收缩素八肽水平在亚慢性抗精神病药物治疗后会发生变化。

Cholecystokinin octapeptide levels in rat brain are changed after subchronic neuroleptic treatment.

作者信息

Frey P

出版信息

Eur J Pharmacol. 1983 Nov 11;95(1-2):87-92. doi: 10.1016/0014-2999(83)90270-4.

Abstract

Cholecystokinin octapeptide sulfate (CCK-8-S), nonsulfated cholecystokinin octapeptide (CCK-8-NS) and cholecystokinin tetrapeptide (CCK-4) levels in rat brain were measured by a combination of high pressure liquid chromatography (HPLC) and radioimmunoassay (RIA) after acute and subchronic treatment of the animals with haloperidol. CCK levels did not change after acute treatment. However, CCK-8-S concentrations were increased in the striatum and the mesolimbic system after two weeks of haloperidol treatment and remained increased after four weeks of haloperidol treatment. A transient decrease in CCK-8-S concentrations was observed in the cortex. Treatment with chlorpromazine or clozapine gave similar results. No changes in CCK-8-NS or CCK-4 concentrations were seen in any of the experiments.

摘要

在用氟哌啶醇对大鼠进行急性和亚慢性处理后,通过高压液相色谱法(HPLC)和放射免疫分析法(RIA)相结合的方法,测定了大鼠脑中的硫酸缩胆囊素八肽(CCK-8-S)、非硫酸化缩胆囊素八肽(CCK-8-NS)和缩胆囊素四肽(CCK-4)水平。急性处理后CCK水平未发生变化。然而,在氟哌啶醇处理两周后,纹状体和中脑边缘系统中的CCK-8-S浓度升高,且在氟哌啶醇处理四周后仍保持升高。在皮质中观察到CCK-8-S浓度出现短暂下降。用氯丙嗪或氯氮平处理也得到了类似的结果。在任何实验中均未观察到CCK-8-NS或CCK-4浓度的变化。

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