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氟哌啶醇和阿立哌唑对大鼠海马体和前额叶皮质中脑源性神经营养因子(BDNF)及糖皮质激素受体水平的影响:慢性轻度应激的作用

Haloperidol and aripiprazole impact on the BDNF and glucocorticoid receptor levels in the rat hippocampus and prefrontal cortex: effect of the chronic mild stress.

作者信息

Osacka Jana, Koprdova Romana, Tillinger Andrej, Pirnik Zdenko, Kiss Alexander

机构信息

Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of Sciences, Bratislava, Slovakia.

Institute of Experimental Pharmacology and Toxicology, Centre of Experimental Medicine, Slovak Academy of Sciences, Bratislava, Slovak Republic.

出版信息

Endocr Regul. 2021 Sep 13;55(3):153-162. doi: 10.2478/enr-2021-0016.

Abstract

Changes in the brain derived neurotrophic factor (BDNF) and glucocorticoid receptor (GR) expression in the prefrontal cortex (PFC) and hippocampus (HIP) are associated with psychiatric diseases and stress response. Chronic mild stress (CMS) may alter BDNF as well as GR levels in both the PFC and the HIP. The aim of the present study was to find out whether chronic treatment with a typical antipsychotic haloperidol (HAL) and an atypical antipsychotic aripiprazole (ARI) may modify the CMS effect on the BDNF and GR expression in the above-mentioned structures. The rats were exposed to CMS for 3 weeks and from the 7 day of CMS injected with vehicle (VEH), HAL (1 mg/kg) or ARI (10 mg/kg) for 4 weeks. BDNF and GR mRNA levels were established in the PFC and the HIP by Real Time PCR, whereas, PFC and HIP samples were obtained by punching them from 500 µm thick frozen sections. C-Fos immunoreactivity was analyzed in the PFC and the HIP on 30 µm thick paraformaldehyde fixed sections. Weight gain and corticosterone (CORT) levels were also measured. The CMS and HAL suppressed the BDNF and GR mRNA levels in the PFC. In the HIP, CMS elevated BDNF mRNA levels that were suppressed by HAL and ARI treatments. The CMS decreased the c-Fos immunoreactivity in the PFC in both HAL- and ARI-treated animals. In the HIP, HAL increased the c-Fos immunoreactivity that was again diminished in animals exposed to CMS. Stressed animals gained markedly less weight until the 7 day of CMS, however, later their weight gain did not differ from the unstressed ones or was even higher in CMS+HAL group. Un-stressed HAL and ARI animals gained less weight than the VEH ones. Neither CMS nor HAL/ARI affected the plasma CORT levels. The present data indicate that HAL and ARI in the doses 1 mg/kg or 10 mg/kg, respectively, does not modify the effect of the CMS preconditioning on the BDNF and GR mRNA levels in the PFC or the HIP. However, HAL seems to modify the CMS effect on the HIP activation.

摘要

前额叶皮质(PFC)和海马体(HIP)中脑源性神经营养因子(BDNF)和糖皮质激素受体(GR)表达的变化与精神疾病和应激反应相关。慢性轻度应激(CMS)可能会改变PFC和HIP中BDNF以及GR的水平。本研究的目的是探究使用典型抗精神病药物氟哌啶醇(HAL)和非典型抗精神病药物阿立哌唑(ARI)进行长期治疗是否可以改变CMS对上述结构中BDNF和GR表达的影响。将大鼠暴露于CMS 3周,从CMS第7天开始,分别注射溶剂(VEH)、HAL(1 mg/kg)或ARI(10 mg/kg),持续4周。通过实时PCR测定PFC和HIP中BDNF和GR mRNA水平,而PFC和HIP样本是从500 µm厚的冷冻切片中打孔获得的。在30 µm厚的经多聚甲醛固定的切片上分析PFC和HIP中的C-Fos免疫反应性。还测量了体重增加和皮质酮(CORT)水平。CMS和HAL抑制了PFC中BDNF和GR mRNA水平。在HIP中,CMS升高了BDNF mRNA水平,而HAL和ARI治疗可抑制该水平。在接受HAL和ARI治疗的动物中,CMS均降低了PFC中的C-Fos免疫反应性。在HIP中,HAL增加了C-Fos免疫反应性,而在暴露于CMS的动物中该反应性再次降低。应激动物在CMS第7天之前体重明显增加较少,但之后它们的体重增加与非应激动物没有差异,或者在CMS + HAL组中甚至更高。未应激的HAL和ARI动物比VEH组动物体重增加更少。CMS以及HAL/ARI均未影响血浆CORT水平。目前的数据表明,分别为1 mg/kg或10 mg/kg剂量的HAL和ARI不会改变CMS预处理对PFC或HIP中BDNF和GR mRNA水平的影响。然而,HAL似乎改变了CMS对HIP激活的影响。

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