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Open AccessJournal ArticleDOI

A Role for Kisspeptins in the Regulation of Gonadotropin Secretion in the Mouse

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TLDR
Kisspeptins are products of the KiSS-1 gene, which bind to a G protein-coupled receptor known as GPR54, and it is concluded that kisspeptin-GPR54 signaling may be part of the hypothalamus circuitry that governs the hypothalamic secretion of GnRH.
Abstract
Kisspeptins are products of the KiSS-1 gene, which bind to a G protein-coupled receptor known as GPR54. Mutations or targeted disruptions in the GPR54 gene cause hypogonadotropic hypogonadism in humans and mice, suggesting that kisspeptin signaling may be important for the regulation of gonadotropin secretion. To examine the effects of kisspeptin-54 (metastin) and kisspeptin-10 (the biologically active C-terminal decapeptide) on gonadotropin secretion in the mouse, we administered the kisspeptins directly into the lateral cerebral ventricle of the brain and demonstrated that both peptides stimulate LH secretion. Further characterization of kisspeptin-54 demonstrated that it stimulated both LH and FSH secretion, at doses as low as 1 fmol; moreover, this effect was shown to be blocked by pretreatment with acyline, a potent GnRH antagonist. To learn more about the functional anatomy of kisspeptins, we mapped the distribution of KiSS-1 mRNA in the hypothalamus. We observed that KiSS-1 mRNA is expressed in areas of the hypothalamus implicated in the neuroendocrine regulation of gonadotropin secretion, including the anteroventral periventricular nucleus, the periventricular nucleus, and the arcuate nucleus. We conclude that kisspeptin-GPR54 signaling may be part of the hypothalamic circuitry that governs the hypothalamic secretion of GnRH.

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Journal ArticleDOI

Kisspeptin as a Behavioral Hormone

TL;DR: This review details the emerging roles of kisspeptin signaling in the broader aspects of behavioral, emotional, and cognitive control and informs the pharmacological development ofkisspeptin as a potential therapeutic strategy for individuals suffering from associated reproductive, emotional and cognitive disorders.
Journal ArticleDOI

Exposure of female mice to perfluorooctanoic acid suppresses hypothalamic kisspeptin-reproductive endocrine system through enhanced hepatic fibroblast growth factor 21 synthesis, leading to ovulation failure and prolonged dioestrus.

TL;DR: In vivo evidence is provided that exposure to PFOA (≥2 mg kg‐1) in mice causes down‐regulation of the kisspeptin‐reproductive endocrine system by enhancing PPARα‐mediated hepatic FGF21 expression.
Journal ArticleDOI

Characterization of the receptor binding residues of kisspeptins by positional scanning using peptide photoaffinity probes

TL;DR: The design and synthesis of novel kisspeptin-based photoaffinity probes are reported, and the application to crosslinking experiments for GPR54-expressing cells is reported.
Journal ArticleDOI

Neuroendocrine interactions of the stress and reproductive axes.

TL;DR: The hypothalamo-pituitary-gonadal (HPG) axis is one of the major pathways that is activated during the stress response in the human reproductive system.
Journal ArticleDOI

Serum Kisspeptin levels in unexplained infertility, polycystic ovary syndrome, and male factor infertility.

TL;DR: KP may be treated by KP injection therapies and higher levels of KP may be a reliable marker for AFC and diagnosis of PCOS, according to an observational cohort study conducted.
References
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Book

The Physiology of Reproduction

Ernst Knobil, +1 more
TL;DR: The gametes, fertilization and early embryogenesis the reproductive systems - the female, the male the pituitary and the hypothalmus, and the reproductive processes and their control.
Journal ArticleDOI

The GPR54 gene as a regulator of puberty

TL;DR: Puberty is initiated when gonadotropin-releasing hormone begins to be secreted by the hypothalamus, and complementary genetic approaches in humans and mice identified genetic factors that determine the onset of puberty.
Journal ArticleDOI

Comparative distribution of estrogen receptor-alpha and -beta mRNA in the rat central nervous system.

TL;DR: Comparing the distribution of the classical and novel forms of ER mRNA‐expressing neurons in the central nervous system (CNS) of the rat with in situ hybridization histochemistry provides evidence that the region‐specific expression of ER‐α, ER‐β, or both may be important in determining the physiological responses of neuronal populations to estrogen action.
Journal ArticleDOI

Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

TL;DR: The present study shows that loss of function of GPR54 is a cause of IHH, and it identifies GPR 54 and possibly KiSS1 protein-derived peptide as playing a major and previously unsuspected role in the physiology of the gonadotropic axis.
Journal ArticleDOI

Distribution of androgen and estrogen receptor mRNA‐containing cells in the rat brain: An in situ hybridization study

TL;DR: AR and ER may modulate nonolfactory sensory information as well since labeled cells were found in regions involved in the central relay of somatosensory information, including the mesencephalic nucleus of the trigeminal nerve, the ventral thalamic nuclear group, and the dorsal horn of the spinal cord.
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