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A novel insulin sensitizer drug candidate-BGP-15-can prevent metabolic side effects of atypical antipsychotics

机译:新型胰岛素增敏药物候选药物BGP-15-可以预防非典型抗精神病药的代谢副作用

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摘要

Atypical antipsychotic drugs (AAPD) are widely used to treat severe psychiatric disorders, have well documented metabolic side effects such as disturbances in glucose metabolism, insulin resistance and weight gain. It has been shown that BGP-15, a hydroxylamine derivative with insulin sensitizing activity can prevent AAPD provoked fat accumulation in adipocyte cultures, and insulin resistance in animal experiments and in healthy volunteers. The aim of this study was to compare the preventive effect of BGP-15 with conventional oral antidiabetics on metabolic side effects of AAPDs. We found that BGP-15 that does not belong to either conventional insulin sensitizers or oral antidiabetics, is able to counteract insulin resistance and weight gain provoked by antipsychotic agents in rats while rosiglitazone and metformin were not effective in the applied doses. Our results confirm that BGP-15 is a promising new drug candidate to control the metabolic side effects of atypical antipsychotics. Data indicate that this rat model is suitable to analyze the metabolic side effects of AAPDs and the protective mechanism of BGP-15.
机译:非典型抗精神病药物(AAPD)被广泛用于治疗严重的精神疾病,并具有充分记录的代谢副作用,例如葡萄糖代谢紊乱,胰岛素抵抗和体重增加。已经显示,具有胰岛素敏化活性的羟胺衍生物BGP-15可以防止AAPD引起脂肪在脂肪细胞培养物中的蓄积,并防止动物实验和健康志愿者的胰岛素抵抗。这项研究的目的是比较BGP-15与常规口服降糖药对AAPDs代谢副作用的预防作用。我们发现不属于常规胰岛素敏化剂或口服抗糖尿病药的BGP-15能够抵消大鼠抗胰岛素药和抗精神病药引起的体重增加,而罗格列酮和二甲双胍在所应用的剂量中无效。我们的结果证实BGP-15是控制非典型抗精神病药的代谢副作用的有希望的新药候选者。数据表明,该大鼠模型适用于分析AAPD的代谢副作用和BGP-15的保护机制。

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