Soylu-Kucharz Rana, Adlesic Natalie, Baldo Barbara, Kirik Deniz, Petersén Åsa
Translational Neuroendocrine Research Unit, Department of Experimental Medical Sciences, Lund University, Sweden.
Brain Repair and Imaging in Neural Systems (B.R.A.I.N.S.) Unit, Department of Experimental Medical Sciences Lund University, Sweden.
Sci Rep. 2015 Sep 30;5:14598. doi: 10.1038/srep14598.
Expression of mutant huntingtin (htt) protein has been shown to cause metabolic imbalance in animal models of Huntington disease (HD). The pathways involved are not fully understood but dysfunction of both the hypothalamus and brown adipose tissue (BAT) has been implicated. Here we show that targeted expression of mutant HTT in the hypothalamus leads to loss of the A13 dopaminergic cell group located in the zona incerta and reduced mRNA expression of neuropeptide Y1 receptor in the hypothalamus. Furthermore, this is accompanied by downregulation of uncoupling protein 1 expression and PPARγ coactivator-1 alpha in BAT and a rapid body weight gain. Taken together, our data might provide a mechanistic link between expression of mutant HTT, reduced activity of a hypothalamic dopaminergic pathway and dysfunction of BAT and in part explain the development of an obese phenotype in HD mouse models.
在亨廷顿舞蹈症(HD)动物模型中,突变型亨廷顿蛋白(htt)的表达已被证明会导致代谢失衡。所涉及的途径尚未完全了解,但下丘脑和棕色脂肪组织(BAT)功能障碍均与之相关。在这里,我们表明,下丘脑突变型HTT的靶向表达会导致位于未定带的A13多巴胺能细胞群丧失,以及下丘脑神经肽Y1受体的mRNA表达降低。此外,这伴随着BAT中解偶联蛋白1表达和PPARγ辅激活因子-1α的下调以及体重快速增加。综上所述,我们的数据可能为突变型HTT的表达、下丘脑多巴胺能途径活性降低和BAT功能障碍之间提供了一个机制联系,并部分解释了HD小鼠模型中肥胖表型的发展。