首页> 外文期刊>Alcoholism: Clinical and experimental research >Innate differences in the expression of brain-derived neurotrophic factor in the regions within the extended amygdala between alcohol preferring and nonpreferring rats.
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Innate differences in the expression of brain-derived neurotrophic factor in the regions within the extended amygdala between alcohol preferring and nonpreferring rats.

机译:酒精偏爱和不偏爱大鼠之间杏仁核延伸区域内脑源性神经营养因子表达的先天差异。

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BACKGROUND: Animal lines such as alcohol-preferring (P) and nonpreferring (NP) rats appear to be suitable animal models to investigate the biological basis of alcohol-drinking behaviors. The extended amygdala serves as a neuroanatomical substrate for alcohol-drinking behaviors. Brain-derived neurotrophic factor (BDNF) in the amygdala has been implicated in alcohol-drinking behaviors; however, its expression in the extended amygdala of P and NP rats is unknown. Therefore, we examined the basal expression of BDNF in the extended amygdala of alcohol naive P and NP rats. METHODS: We determined the basal mRNA and protein levels of BDNF by in situ RT-PCR and immuno-histochemical procedure, respectively, in the amygdaloid [central nucleus of amygdala (CeA), medial nucleus of amygdala (MeA), and basolateral amygdala (BLA)], nucleus accumbal (NAc shell and core), and bed nucleus of stria terminalis (BNST) [lateral BNST (lBNST), medial BNST (mBNST), and ventral BNST (vBNST)] brain structures of P and NP rats. Inaddition, we examined the localization of BDNF in neurons using double-immunofluorescence labeling of BDNF with neuron-specific nuclear protein (NeuN) and also determined the number of NeuN-positive neurons in the amygdaloid structures of P and NP rats. RESULTS: The mRNA and protein levels of BDNF were found to be significantly lower in both the CeA and MeA, but not in the BLA, of P compared with NP rats. We also found that BDNF was expressed in neurons in the amygdaloid structures of P and NP rats. In addition, we found that the number of NeuN-positive neurons was similar in the amygdaloid structures of P and NP rats. Interestingly, the mRNA and protein levels of BDNF were also significantly lower in the lBNST, mBNST, and vBNST of P compared with NP rats. On the other hand, mRNA and protein levels of BDNF were similar in the NAc shell and core structures of P and NP rats. CONCLUSIONS: P and NP rats are selectively bred for higher and lower alcohol preference, respectively; therefore it is possible that lowerBDNF levels in the amygdaloid and BNST structures may be associated with the excessive alcohol-drinking behaviors of P rats.
机译:背景:喜欢酒精(P)和不喜欢酒精(NP)的大鼠等动物系似乎是研究饮酒行为生物学基础的合适动物模型。扩展的杏仁核可作为饮酒行为的神经解剖学基质。杏仁核中的脑源性神经营养因子(BDNF)与饮酒行为有关。但是,它在P和NP大鼠的延伸杏仁核中的表达尚不清楚。因此,我们研究了初次饮酒的P和NP大鼠的杏仁核中BDNF的基础表达。方法:我们通过原位RT-PCR和免疫组化方法分别测定了杏仁核[杏仁核的中央核(CeA),杏仁核的内侧核(MeA)和基底外侧杏仁核( BLA)],P和NP大鼠的末端结构的纹状体核(NAc壳和核)和终末纹的床核(BNST)[外侧BNST(lBNST),内侧BNST(mBNST)和腹侧BNST(vBNST)]脑结构。此外,我们使用神经元特异性核蛋白(NeuN)对BDNF进行双重免疫荧光标记,检查了BDNF在神经元中的定位,并确定了P和NP大鼠杏仁体结构中NeuN阳性神经元的数量。结果:与NP大鼠相比,P的CeA和MeA中BDNF的mRNA和蛋白质水平均显着降低,但BLA中的BDNF的mRNA和蛋白水平均显着降低。我们还发现BDNF在P和NP大鼠的杏仁状结构的神经元中表达。此外,我们发现,P和NP大鼠的杏仁状结构中NeuN阳性神经元的数量相似。有趣的是,与NP大鼠相比,P的lBNST,mBNST和vBNST中BDNF的mRNA和蛋白质水平也显着降低。另一方面,P和NP大鼠的NAc外壳和核​​心结构中BDNF的mRNA和蛋白水平相似。结论:分别对P和NP大鼠分别进行了较高和较低酒精偏好的饲养。因此,杏仁核和BNST结构中较低的BDNF水平可能与P大鼠过度饮酒行为有关。

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