在 MK-801 诱导的精神分裂症大鼠模型中脂肪动情激素/红色素浓缩激素家族肽的神经化学效应

Şeyma Nur BAŞARIR BOZKURT, O. Mutlu, Daniel BERMEJO RODRİGUEZ, David Kacer, P. Tanyeri, Pınar Cobantürk, Karel Vales
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摘要

目的脂肪动情激素(AKH)在昆虫的糖和脂质代谢中发挥作用。以往对 AKH 的研究表明,在精神分裂症大鼠模型中,AKH 可改善大鼠的记忆力;在大鼠嗅球切除术模型中,AKH 可改善大鼠的记忆力,减少抑郁。在本研究中,我们调查了脂肪动情激素/红色素浓缩激素(AKH/RPCH)家族多肽对精神分裂症大鼠模型中脑神经递质水平和脑神经化学的影响。材料与方法:我们在天真大鼠和 MK-801 诱导的精神分裂症大鼠模型中连续 4 天亚周期给药 AKH/RPCH 肽。使用液相色谱-质谱仪对大鼠神经化学进行了靶向和非靶向分析:结果:AKH 显著降低了 MK-801 肽处理大鼠特有的脑谷氨酸水平升高。此外,AKH 还能提高天真大鼠和 MK-801 大鼠的脑多巴胺水平。代谢组学研究表明,AKH影响脂质和谷氨酸代谢,而高卤素则在糖代谢和炎症中发挥作用:根据我们的研究结果,AKH 可能会影响多巴胺能和谷氨酸能系统,并逆转 MK-801 的作用,可能会影响 NMDA 受体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurochemical Effects of the Adipokinetic Hormone/Red Pigment Concentrating Hormone Family of Peptides in MK-801-Induced Schizophrenia Rat Model
Objective: Adipokinetic hormone (AKH) plays a role in sugar and lipid metabolism in insects. Previous studies of AKH showed memory improvements in a schizophrenia rat model that displayed memory impairment and reduced depression in a rat olfactory bulbectomy model. In this study, we investigated the effects of the adipokinetic hormone/red pigment-concentrating hormone (AKH/RPCH) family of peptides on brain neurotransmitter levels and brain neurochemistry in a schizophrenia rat model. Materials and Methods: We administered AKH/RPCH peptides for 4 days sub-chronically, both in naive rats and also in the MK-801-induced schizophrenia rat model. Liquid chromatography-mass spectrometry apparatus was used for targeted and untargeted analysis of rat neurochemistry. Results: Increased brain glutamate levels characteristic of MK-801 peptide-treated rats were significantly reduced by AKH. Furthermore, AKH also increased brain dopamine levels in both naive and MK-801 rats. Metabolomic studies have shown that AKH affects lipid and glutamate metabolism, while hypertrehalosaemic hormone plays a role in sugar metabolism and inflammation. Conclusion: According to our results, AKH might affect dopaminergic and glutamatergic systems and reverse the effects of MK-801, possibly affecting NMDA receptors.
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