Paraventricular Dynorphin A Neurons Mediate LH Pulse Suppression Induced by Hindbrain Glucoprivation in Female Rats

被引:23
|
作者
Tsuchida, Hitomi [1 ]
Mostari, Parvin [1 ]
Yamada, Koki [1 ]
Miyazaki, Sae [1 ]
Enomoto, Yuki [1 ]
Inoue, Naoko [1 ]
Uenoyama, Yoshihisa [1 ]
Tsukamura, Hiroko [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Lab Anim Reprod, Nagoya, Aichi 4648601, Japan
基金
日本学术振兴会;
关键词
dynorphin A receptor; Kiss1; malnutrition; LUTEINIZING-HORMONE SECRETION; CORTICOTROPIN-RELEASING HORMONE; FASTING-INDUCED SUPPRESSION; CHRONIC FOOD RESTRICTION; KAPPA-OPIOID RECEPTOR; ARCUATE NUCLEUS; GLUCOSE AVAILABILITY; PULSATILE SECRETION; KISSPEPTIN NEURONS; NEGATIVE FEEDBACK;
D O I
10.1210/endocr/bqaa161
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Malnutrition suppresses reproductive functions in mammals, which is considered to be mostly due to the inhibition of pulsatile gonadotropin-releasing hormone (GnRH)/gonadotropin secretion. Accumulating evidence suggests that kisspeptin neurons in the arcuate nucleus (ARC) play a critical role in the regulation of pulsatile GnRH/gonadotropin release. The present study aimed to examine if the hypothalamic dynorphin A (Dyn) neurons mediate the suppression of GnRH/luteinizing hormone (LH) pulses during malnutrition. Ovariectomized rats treated with a negative feedback level of estradiol-17 beta-treated (OVX+E2) were administered with intravenous (iv) or fourth cerebroventricle (4V) 2-deoxy-D-glucose (2DG), an inhibitor of glucose utilization, to serve as a malnutrition model. Central administration of a Dyn receptor antagonist blocked the iv- or 4V-2DG-induced suppression of LH pulses in OVX+E2 rats. The 4V 2DG administration significantly increased the number of Pdyn (Dyn gene)-positive cells co-expressing fos in the paraventricular nucleus (PVN), but not in the ARC and supraoptic nucleus (SON), and the iv 2DG treatment significantly increased the number of fos and Pdyn-co-expressing cells in the PVN and SON, but decreased it in the ARC. The E2 treatment significantly increased Pdyn expression in the PVN, but not in the ARC and SON. Double in situ hybridization for Kiss1 (kisspeptin gene) and Oprk1 (Dyn receptor gene) revealed that around 60% of ARC Kiss1-expressing cells co-expressed Oprk1. These results suggest that the PVN Dyn neurons, at least in part, mediate LH pulse suppression induced by the hindbrain or peripheral glucoprivation, and Dyn neurons may directly suppress the ARC kisspeptin neurons in female rats.
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页数:18
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