Aging-related changes in RP3V kisspeptin neurons predate the reduced activation of GnRH neurons during the early reproductive decline in female mice

被引:36
作者
Zhang, Jing [1 ,3 ]
Yang, Lumeng [1 ]
Lin, Nan [1 ]
Pan, Xiaodong [1 ,2 ]
Zhu, Yuangui [1 ]
Chen, Xiaochun [1 ,2 ,3 ]
机构
[1] Fujian Med Univ, Affiliated Union Hosp, Fujian Inst Geriatr, Key Lab Brain Aging & Neurodegenerat Dis, Fuzhou 350001, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Union Hosp, Dept Neurol, Fuzhou 350001, Fujian, Peoples R China
[3] Fujian Med Univ, Fujian Key Lab Mol Neurol, Fuzhou 350001, Fujian, Peoples R China
关键词
Aging; GnRH; Kisspeptin; Estrogen receptor-alpha; Progesterone receptor; c-Fos; ESTROGEN-POSITIVE FEEDBACK; LUTEINIZING-HORMONE SURGE; KISS1; GENE-EXPRESSION; MIDDLE-AGED RATS; RECEPTOR-ALPHA; PREOPTIC AREA; LHRH NEURONS; MOUSE-BRAIN; IN-VIVO; P16(INK4A);
D O I
10.1016/j.neurobiolaging.2013.08.038
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Kisspeptin neurons in the rostral periventricular area of the third ventricle (RP3V) play a key role in relaying the positive feedback effects of estradiol that activate gonadotropin-releasing hormone (GnRH) neurons and drive a surge in the GnRH/luteinizing hormone (LH) level. However, the precise role of kisspeptin neurons during female reproductive senescence remains unclear. Focusing on middle-aged intact female mice with irregular estrous cycles, we found a parallel decline in c-Fos-positive kisspeptin neurons and c-Fos-positive GnRH neurons at the time of the GnRH/LH surge. Furthermore, in kisspeptin neurons, the expression of estrogen receptor alpha (ER alpha), but not progesterone receptor (PR), decreased with age. Interestingly, some kisspeptin neurons in the RP3V, but none of the GnRH neurons in the rostral preoptic area (rPOA), had a characteristic cellular senescence in middle-aged mice and old mice. These data suggest that, among the groups of neurons involved in reproductive control, the kisspeptin neurons in the RP3V are likely among the earliest to undergo aging processes and thus participate in initiating the early reproductive decline. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:655 / 668
页数:14
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