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作 者:韦姗姗[1] 杨和金 黄加文 陆雪萍 彭玲芳 王庆国[1]
机构地区:[1]北京中医药大学基础医学院,100029 [2]云南省药物研究所药物筛选中心,昆明650111
出 处:《国际免疫学杂志》2016年第3期205-209,共5页International Journal of Immunology
基 金:国家重点基础研究发展计划(973计划)(2011CB505100)
摘 要:目的高台应激是一种不可逃避应激,是研究应激对机体神经生理病理变化的重要模型。本研究对急性高台应激后神经内分泌激素、受体表达、脑神经递质变化以及地西泮的干预作用进行探讨。方法大鼠随机分为空白对照组、应激+地西泮(DAP)组与应激+溶剂组。后两组于应激前30min分别腹腔注射地西泮2mg/kg与等量生理盐水。采用酶联免疫法测量应激后各组的血浆促。肾上腺皮质激素(ACTH)、血清皮质酮(CORT)水平;采用实时定量PCR测量下丘脑促肾上腺皮质激素分泌激素(CRH)mRNA、海马糖皮质激素受体(GR)mRNA、盐皮质激素受体(MR)mRNA、5-羟色胺1a受体(5-HT1aR)mRNA水平;采用高效液相色谱电化学法测量大脑皮层匀浆液中去甲肾上腺素(NE)、多巴胺(DA)、5-羟色胺(5-HT)及其代谢产物5一羟吲哚乙酸(5-HIAA)水平。结果与空白组相比,应激+溶剂组大鼠血浆ACTH、血清CORT以及海马5-HT1aRmRNA水平升高(P均〈0.05),此变化可由DAP逆转(P均〈0.05)。此外,DAP还可降低应激后的下丘脑CRHmRNA,海马GRmRNA以及MRmRNA水平(P均〈0.05)。然而大脑皮层匀浆液中NE、DA、5-HT、5-HIAA在应激后无变化。结论急性高台应激可引起大鼠相关神经内分泌激素与受体表达变化,且该效应可被DAP逆转。Objects Elevated platform stress is an important model to study the acute stress-induced neurophysiologic changes of organisms. In this study, we investigated the effect of the elevated platform stress and/or diazepam (DAP) on the expression of neuroendocrine hormones, receptors, and neurotransmitters in rats. Methods Rats were randomly divided into three groups: naive group, stress + DAP group, and stress + vehicle group. The last two groups were given DAP ( 2 mg/kg in vehicle, i. p. ) and vehicle ( i. p. ) 30 min a- head of stress, respectively. The levels of plasma adrenocorticotropie hormone (ACTH) and serum eorticoster- one (CORT) were determined by enzyme-linked immuno sorbent assay (ELISA). The mRNA level of hypo- thalamus eorticotropin releasing hormone ( CRH), hippocampus glueoeorticoid receptors ( GR), mineralocorti- coid receptor (MR), and 5-hydroxytryptophan receptor (5-HT1 aR) were determined by quantitative real-time PCR. The amount of norepinephrine (NE), dopamine (DA), 5-hydroxytryptophan (5-HT), and 5-hydroxyin- doleacetic acid (5-HIAA) were determined by HPLC-Electrochemical Detection. Results Compared with the naive group, levels of plasma ACTH, serum CORT, and hippocampus 5-HT1 aR mRNA in the last two groups increased after exposure to the stress ( all p 〈 0.05 ). Such increases could be reversed by DAP ( all P 〈 0. 05 ). In additional, DAP could down-regulate the mRNA level of hypothalamus CRH, hippocampus GR and MR ( all P 〈 0.05). Meanwhile, elevated stress and DAP have no significant effect on the NE, DA, 5-HT, and 5-HIAA level. Conclusion The acute elevated platform stress induces higher levels of neuroendoerine hormones and re- ceptors in rats. This effect can be reversed by DAP.
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