4.5 Article

Metabolic control of puberty onset: New players, new mechanisms

Journal

MOLECULAR AND CELLULAR ENDOCRINOLOGY
Volume 324, Issue 1-2, Pages 87-94

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2009.12.018

Keywords

Puberty; Energy balance; Leptin; Ghrelin; Kiss1; Kisspeptins; GPR54; mTOR; Crtc1

Funding

  1. Ministerio de Ciencia e Innovacion, Spain [BFU 2005-07446, BFU 2008-00984]
  2. Instituto de Salud Carlos III, Ministerio de Sanidad, Spain [RCMN C03/08, PI042082]
  3. Junta de Andalucia, Spain [P08-CVI-03788]
  4. EU [EDEN QLK4-CT-2002-00603, DEER FP7-ENV-2007-1]

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Puberty, as the end-point of a complex series of maturational events affecting the components of the hypothalamic-pituitary-gonadal (HPG) axis, is gated by the state of body energy reserves and sensitive to different metabolic cues; conditions of severe metabolic stress and energy unbalance (from anorexia to morbid obesity) being commonly linked to perturbation of the onset of puberty. In the last two decades, the neuroendocrine mechanisms responsible for the tight coupling between energy homeostasis and puberty onset have begun to be deciphered. These seemingly involve a plethora of metabolic hormones and neuropeptides, which impinge and integrate (mostly) at the hypothalamic centers governing reproduction. Yet, characterization of the mechanisms of action of such regulators (and even their nature and physiological relevance) still remains incomplete. In this review, we will summarize some recent developments in our knowledge of the effects and mechanisms of action of two key metabolic hormones, leptin and ghrelin, in the control of puberty onset. In addition, the roles of the hypothalamic Kiss1 system in the metabolic gating of puberty will be reviewed, with special attention to its regulation by leptin and the recent identification of the putative roles of Crtc1 and mTOR signaling as molecular conduits for the metabolic control of Kiss1 expression. Elucidation of these novel players and regulatory mechanisms will help for a better understanding of the determinants of the timing of puberty, and its eventual alterations in adverse metabolic conditions. (C) 2009 Elsevier Ireland Ltd. All rights reserved.

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