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早期丰富环境可预防 MK-801 诱导的精神分裂症动物模型的认知障碍:海马脑源性神经营养因子的作用。

Early enriched environment prevents cognitive impairment in an animal model of schizophrenia induced by MK-801: Role of hippocampal BDNF.

机构信息

Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.

Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Brain Res. 2019 May 15;1711:115-119. doi: 10.1016/j.brainres.2019.01.023. Epub 2019 Jan 21.

Abstract

Early life experience has long-lasting effects on brain and behaviour. This study aims to investigate the long-term effects of enriched environment (EE), which was imposed during the animals' development, on their recognition memory as well as hippocampal levels of brain-derived neurotrophic factor (BDNF), in an animal model of schizophrenia induced by chronic postnatal administration of MK-801. Forty male and female rat pups were separated in four distinct groups for each sex (n = 10). The rats were injected with MK-801 (1 mg/kg) or saline (1 cc/kg) on their postnatal days (P) 6-10. MK-801 and Control rats were maintained in standard or enriched cages (containing toys, tunnels, running wheels, and climbing frame), from their birth up to the time of behavioral experiments at P60. Neonatal challenge with MK-801 significantly impaired novel object recognition (NOR) in both male and female animals. EE exposure reversed the recognition memory only in male rats. MK-801 resulted in decreased levels of BDNF in the hippocampus, and EE exposure restored the decreased level. Our results provide evidence that BDNF plays an important role in pathophysiology of schizophrenia in the present animal model, and is a possible mechanism through which early EE can enhance the cognitive functions.

摘要

早期生活经历对大脑和行为有持久的影响。本研究旨在探讨丰富环境(EE)对精神分裂症动物模型认知记忆的长期影响,该模型是通过在动物发育期间给予慢性 postnatal administration of MK-801 诱导的。40 只雄性和雌性幼鼠被分为四个不同的组(n=10)。幼鼠在出生后的第 6-10 天(P)接受 MK-801(1mg/kg)或生理盐水(1cc/kg)注射。MK-801 和对照大鼠从出生到 P60 进行行为实验时,分别在标准或丰富环境笼中(含有玩具、隧道、跑步轮和攀爬架)饲养。新生期接受 MK-801 挑战显著损害了雄性和雌性幼鼠的新物体识别(NOR)。EE 暴露仅在雄性大鼠中逆转了识别记忆。MK-801 导致海马体 BDNF 水平降低,而 EE 暴露恢复了降低的水平。我们的结果提供了证据,表明 BDNF 在本动物模型的精神分裂症发病机制中发挥重要作用,并且是早期 EE 可以增强认知功能的可能机制。

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