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Distinct Patterns of Neuropeptide Gene Expression in the Lateral Hypothalamic Area and Arcuate Nucleus Are Associated with Dehydration-Induced Anorexia

机译:下丘脑外侧区和弓状核中神经肽基因表达的不同模式与脱水诱导的厌食症相关。

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摘要

We have investigated the hormonal and hypothalamic neuropeptidergic substrates of dehydration-associated anorexia. In situhybridization and hormone analyses of anorexic and paired food-restricted rats revealed two distinct profiles. First, both groups had the characteristic gene expression and endocrine signatures usually associated with starvation: increased neuropeptide Y and decreased proopiomelanocortin and neurotensin mRNAs in the arcuate nucleus (ARH); increased circulating glucocorticoid but reduced leptin and insulin. Dehydrated animals are strongly anorexic despite these attributes, showing that the output of leptin- and insulin-sensitive ARH neurons that ordinarily stimulate eating must be inhibited. The second pattern occurred only in anorexic animals and had two components: (1) reduced corticotropin-releasing hormone (CRH) mRNA in the neuroendocrine paraventricular nucleus (PVH) and (2) increased CRH and neurotensin mRNAs in the lateral hypothalamic (LHA) and retrochiasmatic areas. However, neither corticosterone nor suppressed PVH CRH gene expression is required for anorexia after dehydration because PVH CRH mRNA in dehydrated adrenalectomized animals is unchanged from euhydrated adrenalectomized controls. We also showed that LHA CRH mRNA was strongly correlated with the intensity of anorexia, increased LHA CRH gene expression preceded the onset of anorexia, and dehydrated adrenalectomized animals (which also develop anorexia) had elevated LHA CRH gene expression with a distribution pattern similar to intact animals. Finally, we identified specific efferents from the CRH-containing region of the LHA to the PVH, thereby providing a neuroanatomical framework for the integration by the PVH of neuropeptidergic signals from the ARH and the LHA. Together, these observations suggest that CRH and neurotensin neurons in the LHA constitute a novel anatomical substrate for their well known anorexic effects.
机译:我们研究了与脱水相关的厌食症的激素和下丘脑神经肽能底物。在厌食症和成对食物受限的大鼠的原位杂交和激素分析中发现了两个不同的特征。首先,两组都具有通常与饥饿相关的特征基因表达和内分泌特征:弓形核(ARH)中神经肽Y升高,原黑素皮质素和神经降压素mRNA降低;循环糖皮质激素增加,但瘦素和胰岛素减少。尽管具有这些属性,脱水动物还是强烈厌食症,这表明必须抑制通常刺激饮食的对瘦素和胰岛素敏感的ARH神经元的输出。第二种模式仅发生在厌食症动物中,并且具有两个组成部分:(1)神经内分泌脑室旁核(PVH)中促肾上腺皮质激素释放激素(CRH)mRNA的降低和(2)下丘脑外侧(LHA)中CRH和神经降压素mRNA的升高和后弯部位。但是,脱水后的厌食症既不需要皮质酮也不抑制PVH CRH基因的表达,因为脱水肾上腺切除术动物体内的PVH CRH mRNA与正常水合肾上腺切除术对照组相比没有变化。我们还显示,LHA CRH mRNA与厌食症的强度密切相关,在厌食症发作之前LHA CRH基因表达增加,并且脱水肾上腺切除动物(也发展为厌食症)的LHA CRH基因表达升高,分布模式与完整相似动物。最后,我们确定了从LHA的含有CRH的区域到PVH的特定传出,从而为PVH整合了来自ARH和LHA的神经肽能信号提供了神经解剖学框架。总之,这些观察结果表明,LHA中的CRH和神经降压素神经元因其众所周知的厌食作用而构成了一种新型的解剖学底物。

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