The Role of Neurokinin B Signalling in Reproductive Neuroendocrinology

被引:47
作者
Grachev, P. [1 ]
Millar, R. P. [2 ,3 ,4 ]
O'Byrne, K. T. [1 ]
机构
[1] Kings Coll London, Div Womens Hlth, Sch Med, London SE1 1UL, England
[2] Univ Edinburgh, Ctr Integrat Physiol, Edinburgh, Midlothian, Scotland
[3] Univ Pretoria, Mammal Res Inst, ZA-0002 Pretoria, South Africa
[4] Univ Cape Town, UCT MRC Receptor Biol Grp, ZA-7925 Cape Town, South Africa
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Neurokinin B; Kisspeptin; Dynorphin A; Gonadotropin-releasing hormone; Luteinising hormone; GONADOTROPIN-RELEASING-HORMONE; MONKEY MACACA-MULATTA; KAPPA-OPIOID RECEPTORS; GNRH PULSE-GENERATOR; MEDIAL PREOPTIC AREA; ESTROGEN NEGATIVE FEEDBACK; FEMALE MOUSE-BRAIN; LUTEINIZING-HORMONE; ARCUATE NUCLEUS; RHESUS-MONKEY;
D O I
10.1159/000357734
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The KNDy neuropeptides, kisspeptin, neurokinin B (NKB) and dynorphin A (Dyn), have been implicated in regulating pulsatile luteinising hormone (LH) secretion. Studies of the interactions between KNDy signalling systems, however, are currently few. Although the stimulatory effect of kisspeptin and the inhibitory effect of Dyn on the gonadotropin-releasing hormone pulse generator are widely accepted, the effects of NKB in rodents are variable and sometimes controversial. Literature describing increased LH secretion in response to NKB receptor agonism predominates and is in line with human physiology, as well as the pathophysiology of pubertal failure associated with disruption of NKB signalling. However, the robust suppression of the LH pulse, induced by the same treatment under hypoestrogenic conditions, may hold clues as to the mechanisms of reproductive inhibition under pathological conditions. This review discusses the recent evidence for this paradox and outlines a revised working model incorporating the mechanisms by which KNDy neuropeptides modulate the reproductive axis. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:7 / 17
页数:11
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