Guan X M, Yu H, Trumbauer M, Frazier E, Van der Ploeg L H, Chen H
Department of Obesity Research, Merck Research Laboratories, Rahway, NJ 07065, USA.
Neuroreport. 1998 Oct 26;9(15):3415-9. doi: 10.1097/00001756-199810260-00015.
Alterations of hypothalamic neuropeptide Y(NPY) and melanocortinergic functions in diet-induced obese (DIO) C57BL/6J mice were investigated by in situ hybridization. Compared with controls, the DIO mice displayed a profound induction (approximately 40-fold) of NPY expression in the dorsomedial (DMH) and ventromedial (VMH) hypothalamic nuclei, whereas the level of NPY mRNA in the arcuate nucleus (ARC) was reduced by 44%. The expression of pro-opiomelanocortin (POMC) and agouti-related protein was not significantly altered in the ARC of obese mice. Both excess body weight gain and altered hypothalamic NPY expression were reversible. We propose that the highly induced NPY expression in DMH and/or VMH may be a contributing etiological factor for the development of obesity and leptin resistance in the DIO mice.
通过原位杂交技术研究了饮食诱导肥胖(DIO)的C57BL/6J小鼠下丘脑神经肽Y(NPY)和黑皮质素能功能的变化。与对照组相比,DIO小鼠在背内侧(DMH)和腹内侧(VMH)下丘脑核中NPY表达显著增加(约40倍),而弓状核(ARC)中NPY mRNA水平降低了44%。肥胖小鼠ARC中阿黑皮素原(POMC)和刺鼠相关蛋白的表达没有显著改变。体重过度增加和下丘脑NPY表达改变都是可逆的。我们认为,DMH和/或VMH中高度诱导的NPY表达可能是DIO小鼠肥胖和瘦素抵抗发生的一个致病因素。