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应激和糖皮质激素会影响海马体中脑源性神经营养因子和神经营养素-3信使核糖核酸的表达。

Stress and glucocorticoids affect the expression of brain-derived neurotrophic factor and neurotrophin-3 mRNAs in the hippocampus.

作者信息

Smith M A, Makino S, Kvetnansky R, Post R M

机构信息

Biological Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.

出版信息

J Neurosci. 1995 Mar;15(3 Pt 1):1768-77. doi: 10.1523/JNEUROSCI.15-03-01768.1995.

DOI:10.1523/JNEUROSCI.15-03-01768.1995
PMID:7891134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6578156/
Abstract

Chronic stress produces structural changes and neuronal damage especially in the hippocampus. Because neurotrophic factors affect neuron survival, we questioned whether they might be relevant to the heightened vulnerability of hippocampal neurons following stress. To begin investigating this possibility, we examined the effects of immobilization stress (2 hr/d) on the expression of neurotrophic factors in rat brains using in situ hybridization. We found that single or repeated immobilization markedly reduced brain-derived neurotrophic factor (BDNF) mRNA levels in the dentate gyrus and hippocampus. In contrast, NT-3 mRNA levels were increased in the dentate gyrus and hippocampus in response to repeated but not acute stress. Stress did not affect the expression of neurotrophin-4, or tyrosine receptor kinases (trkB or C). Corticosterone negative feedback may have contributed in part to the stress-induced decreases in BDNF mRNA levels, but stress still decreased BDNF in the dentate gyrus in adrenalectomized rats suggesting that additional components of the stress response must also contribute to the observed changes in BDNF. However, corticosterone-mediated increases in NT-3 mRNA expression appeared to be primarily responsible for the effects of stress on NT-3. These findings demonstrate that BDNF and NT-3 are stress-responsive genes and raise the possibility that alterations in the expression of these or other growth factors might be important in producing some of the physiological and pathophysiological effects of stress in the hippocampus.

摘要

慢性应激会产生结构变化和神经元损伤,尤其是在海马体中。由于神经营养因子会影响神经元的存活,我们不禁要问,它们是否与应激后海马神经元的更高易损性有关。为了开始研究这种可能性,我们使用原位杂交技术检测了固定应激(每天2小时)对大鼠大脑中神经营养因子表达的影响。我们发现,单次或反复固定会显著降低齿状回和海马体中脑源性神经营养因子(BDNF)的mRNA水平。相比之下,响应反复而非急性应激时,齿状回和海马体中的NT-3 mRNA水平会升高。应激不会影响神经营养蛋白-4或酪氨酸受体激酶(trkB或C)的表达。皮质酮的负反馈可能部分导致了应激诱导的BDNF mRNA水平下降,但在肾上腺切除的大鼠中,应激仍会降低齿状回中的BDNF,这表明应激反应的其他成分也必定导致了观察到的BDNF变化。然而,皮质酮介导的NT-3 mRNA表达增加似乎是应激对NT-3产生影响的主要原因。这些发现表明BDNF和NT-3是应激反应基因,并增加了一种可能性,即这些或其他生长因子表达的改变可能在产生应激对海马体的一些生理和病理生理影响方面很重要。