Regulation of gonadotropin-releasing hormone neurons by glucose

被引:35
|
作者
Roland, Alison V. [1 ]
Moenter, Suzanne M. [2 ,3 ,4 ]
机构
[1] Univ Penn, Dept Anim Biol, Philadelphia, PA 19104 USA
[2] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Obstet & Gynecol, Ann Arbor, MI 48109 USA
来源
基金
美国国家卫生研究院;
关键词
PULSATILE LUTEINIZING-HORMONE; PULSE-GENERATOR ACTIVITY; INSULIN-INDUCED HYPOGLYCEMIA; ACTIVATED PROTEIN-KINASE; PRIMED OVARIECTOMIZED RAT; K-ATP CHANNELS; LH-SECRETION; RHESUS-MONKEY; INDUCED SUPPRESSION; ENERGY HOMEOSTASIS;
D O I
10.1016/j.tem.2011.07.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reproduction is influenced by energy balance, but the physiological pathways mediating their relationship have not been fully elucidated. As the central regulators of fertility, gonadotropin-releasing hormone (GnRH) neurons integrate numerous physiological signals, including metabolic cues. Circulating glucose levels regulate GnRH release and might in part mediate the effects of negative energy balance on fertility. Existing evidence suggests that neural pathways originating in the hind-brain, as well as in the hypothalamic feeding nuclei, transmit information concerning glucose availability to GnRH neurons. Here we review recent evidence suggesting that GnRH neurons might directly sense changes in glucose availability by a mechanism involving AMP-activated protein kinase. These findings expand our understanding of how metabolic signaling in the brain regulates reproduction.
引用
收藏
页码:443 / 449
页数:7
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