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Metformin attenuates antipsychotic-induced metabolic dysfunctions in MK801-induced schizophrenia-like rats

机译:二甲双胍在MK801诱导的精神分裂症样大鼠中衰减抗精神病药诱导的代谢功能障碍

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Rationale Second-generation antipsychotics are the first-line medications prescribed for schizophrenic patients; however, some of them, such as olanzapine and risperidone, may induce metabolic dysfunctions during short-term treatment. Metformin is an effective adjuvant that attenuates antipsychotic-induced metabolic dysfunctions (AIMD) in clinical practice. Whether metformin can reverse AIMD and whether metformin affects the therapeutic effects of antipsychotics in animal models of schizophrenia are questions that still need to be investigated. Methods In this study, an animal model of schizophrenia was established by consecutive injections of MK801 during the neurodevelopmental period. In adulthood, different dosages of olanzapine or risperidone treatment were administered to the schizophrenia model animals for 14 days. Both therapeutic effects and metabolic adverse effects were measured by behavioral tests, histopathological tests, and biochemical tests. The coadministration of different doses of metformin with olanzapine or risperidone was used to evaluate the effects of metformin on both AIMD and the therapeutic effect of those antipsychotics. Results The MK801-treated rats showed schizophrenia-like behavior and variations in the shape and volume of the hippocampus. Both olanzapine and risperidone reversed the MK801-induced behavioral abnormalities as the dosage increased; however, they degenerated the hepatocytes in the liver and influenced the blood lipid levels and blood glucose levels. The coadministration of metformin did not affect the therapeutic effects of olanzapine or risperidone on behavioral abnormalities but attenuated the metabolic dysfunctions induced by those antipsychotics. Conclusion Metformin attenuated the olanzapine- and risperidone-induced metabolic dysfunctions in MK801-induced schizophrenia-like rats without reducing the therapeutic effects of the antipsychotics.
机译:理由第二代抗精神病药是精神分裂症患者规定的一线药物;然而,其中一些,例如奥氮藻和立妥酮,可能在短期治疗期间诱导代谢功能障碍。二甲双胍是一种有效的佐剂,可在临床实践中衰减抗精神病药诱导的代谢功能障碍(AIMD)。二甲双胍是否可以逆转,二甲双胍是否影响抗精神病药在精神分裂症的动物模型中是仍然需要调查的问题。方法在本研究中,通过在神经发育期间的MK801进行了连续注射了精神分裂症的动物模型。在成年期间,将不同剂量的奥氮滨或立体酮处理施用于精神分裂症模型动物14天。通过行为测试,组织病理学试验和生物化学测试来测量治疗效果和代谢不良反应。不同剂量二甲双胍与奥氮滨或立牛酮的共同分析用于评估二甲双胍对抗精神病药的治疗效果的影响。结果MK801处理的大鼠表现出精神分裂症状行为和海马形状和体积的变化。奥拉扎宁和利培酮都逆转了MK801诱导的行为异常,因为剂量增加;然而,他们退化了肝脏中的肝细胞并影响了血脂水平和血糖水平。二甲双胍的共同分析不影响奥氮翼或立酮对行为异常的治疗作用,但减弱了这些抗精神病药诱导的代谢功能障碍。结论二甲双胍在MK801诱导的精神分裂症类动物中衰减奥氮平和立体酮诱导的代谢功能障碍,而不降低抗精神病药的治疗效果。

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