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Neuroplasticity-dependent and -independent mechanisms of chronic deep brain stimulation in stressed rats

机译:应激大鼠慢性深部脑刺激的神经可塑性依赖性和非依赖性机制

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摘要

Chronic ventromedial prefrontal cortex (vmPFC) deep brain stimulation (DBS) improves depressive-like behaviour in rats via serotonergic and neurotrophic-related mechanisms. We hypothesise that, in addition to these substrates, DBS-induced increases in hippocampal neurogenesis may also be involved. Our results show that stress-induced behavioural deficits in the sucrose preference test, forced swim test, novelty-suppressed feeding test (NSFT) and elevated plus maze were countered by chronic vmPFC DBS. In addition, stressed rats receiving stimulation had significant increases in hippocampal neurogenesis, PFC and hippocampal brain-derived neurotrophic factor levels. To block neurogenesis, stressed animals given DBS were injected with temozolomide. Such treatment reversed the anxiolytic-like effect of stimulation in the NSFT without significantly affecting performance in other behavioural tests. Taken together, our findings suggest that neuroplastic changes, including neurogenesis, may be involved in specific anxiolytic effects of DBS without affecting its general antidepressant-like response.
机译:慢性腹膜前额叶皮层(vmPFC)深部脑刺激(DBS)通过血清素能和神经营养相关机制改善了大鼠的抑郁样行为。我们假设除这些底物外,DBS诱导的海马神经发生增加也可能涉及。我们的结果表明,慢性vmPFC DBS可以抵消蔗糖偏好测试,强迫游泳测试,新奇抑制喂养测试(NSFT)和高架迷宫中压力引起的行为缺陷。此外,接受刺激的应激大鼠海马神经发生,PFC和海马脑源性神经营养因子水平显着增加。为了阻止神经发生,给给予DBS的应激动物注射替莫唑胺。这种治疗可以逆转NSFT中类似抗焦虑药的刺激作用,而不会显着影响其他行为测试的表现。综上所述,我们的研究结果表明,神经形成性改变,包括神经发生,可能参与了DBS的特定抗焦虑作用,而不影响其一般的抗抑郁样反应。

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