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抗精神病药物对给予地佐环平后神经毒性、脾后皮质中Fos样蛋白表达及c-fos mRNA的影响。

Effects of antipsychotic drugs on neurotoxicity, expression of fos-like protein and c-fos mRNA in the retrosplenial cortex after administration of dizocilpine.

作者信息

Fujimura M, Hashimoto K, Yamagami K

机构信息

Tokyo Laboratories, Pharmaceutical Research Division, Yoshitomi Pharmaceutical Industries, Ltd, Saitama, Iruma, Japan.

出版信息

Eur J Pharmacol. 2000 Jun 9;398(1):1-10. doi: 10.1016/s0014-2999(00)00235-1.

Abstract

In this study, we examined the effect of clozapine, olanzapine, risperidone and haloperidol on the neuropathology (i.e. neuronal vacuolization) and the expression of Fos-like protein and c-fos mRNA in the retrosplenial cortex of female Sprague-Dawley rats induced by the NMDA receptor antagonist dizocilpine. Pretreatment (15 min) with clozapine or olanzapine, but not risperidone or haloperidol, blocked the neuronal vacuolization produced by dizocilpine (0.5 mg/kg, s.c.) in the rat retrosplenial cortex in a dose-dependent manner. Furthermore, pretreatment (15 min) with clozapine or olanzapine, but not risperidone or haloperidol, significantly attenuated the expression of Fos-like protein in the retrosplenial cortex induced by dizocilpine (0.5 mg/kg, s.c.) in a dose-dependent manner. The marked expression of c-fos mRNA in the rat retrosplenial cortex induced by the administration of dizocilpine (0.5 mg/kg, s.c.) was significantly attenuated by pretreatment (15 min) with clozapine (10 mg/kg) or olanzapine (10 mg/kg), but not risperidone (10 mg/kg) or haloperidol (10 mg/kg). The present results suggest that pharmacologically relevant doses of clozapine or olanzapine, but not risperidone or haloperidol, block the neuropathological changes and the expression of Fos-like protein and c-fos mRNA in the rat retrosplenial cortex elicited by the administration of dizocilpine. It is possible that the blockade of dizocilpine-induced neuropathological changes by clozapine and olanzapine may be related to the unique antipsychotic actions of these drugs in schizophrenic patients, although this remains to be verified.

摘要

在本研究中,我们检测了氯氮平、奥氮平、利培酮和氟哌啶醇对由N-甲基-D-天冬氨酸(NMDA)受体拮抗剂地佐环平诱导的雌性Sprague-Dawley大鼠脾后皮质神经病理学(即神经元空泡化)以及Fos样蛋白和c-fos mRNA表达的影响。氯氮平或奥氮平预处理(15分钟),而非利培酮或氟哌啶醇,能以剂量依赖性方式阻断地佐环平(0.5mg/kg,皮下注射)在大鼠脾后皮质产生的神经元空泡化。此外,氯氮平或奥氮平预处理(15分钟),而非利培酮或氟哌啶醇,能以剂量依赖性方式显著减弱地佐环平(0.5mg/kg,皮下注射)诱导的大鼠脾后皮质Fos样蛋白的表达。地佐环平(0.5mg/kg,皮下注射)给药诱导的大鼠脾后皮质c-fos mRNA的显著表达,在氯氮平(10mg/kg)或奥氮平(10mg/kg)预处理(15分钟)后显著减弱,但利培酮(10mg/kg)或氟哌啶醇(10mg/kg)预处理则无此效果。目前的结果表明,药理学相关剂量的氯氮平或奥氮平,而非利培酮或氟哌啶醇,可阻断地佐环平给药引起的大鼠脾后皮质神经病理学变化以及Fos样蛋白和c-fos mRNA的表达。氯氮平和奥氮平对由地佐环平诱导的神经病理学变化的阻断作用,可能与这些药物在精神分裂症患者中的独特抗精神病作用有关,尽管这一点仍有待验证。

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