Abstract

The classic concept of how pituitary GH is regulated by somatostatin and GHRH has changed in recent years, following the discovery of peripheral hormones involved in the regulation of energy homeostasis and mineral homeostasis. These hormones are ghrelin, nesfatins, and klotho. Ghrelin is an orexigenic hormone, released primarily by the gastric mucosa, although it is widely expressed in many different tissues, including the central nervous system and the pituitary. To be active, ghrelin must bind to an n-octanoyl group (n = 8, generally) on serine 3, forming acyl ghrelin which can then bind and activate a G-protein-coupled receptor leading to phospholipase C activation that induces the formation of inositol 1,4,5-triphosphate and diacylglycerol that produce an increase in cytosolic calcium that allows the release of GH. In addition to its direct action on somatotrophs, ghrelin co-localizes with GHRH in several neurons, facilitating its release by inhibiting somatostatin, and acts synergistically with GHRH stimulating the synthesis and secretion of pituitary GH. Gastric ghrelin production declines with age, as does GH. Klotho is an anti-aging agent, produced mainly in the kidneys, whose soluble circulating form directly induces GH secretion through the activation of ERK1/2 and inhibits the inhibitory effect that IGF-I exerts on GH. Children and adults with untreated GH-deficiency show reduced plasma levels of klotho, but treatment with GH restores them to normal values. Deletions or mutations of the Klotho gene affect GH production. Nesfatins 1 and 2 are satiety hormones, they inhibit food intake. They have been found in GH3 cell cultures where they significantly reduce the expression of gh mRNA and that of pituitary-specific positive transcription factor 1, consequently acting as inhibitors of GH production. This is a consequence of the down-regulation of the cAMP/PKA/CREB signaling pathway. Interestingly, nesfatins eliminate the strong positive effect that ghrelin has on GH synthesis and secretion. Throughout this review, we will attempt to broadly analyze the role of these hormones in the complex world of GH regulation, a world in which these hormones already play a very important role.

Highlights

  • Our group was the first to describe in humans the existence of an intrinsichypothalamic-somatotrophic rhythm, sexually dimorphic, that conditions the secretion of growth hormone (GH) [1]

  • GH protein levels the expression of pit-1, and that of the gh gene, by negatively regulating the cAMP/PKA/CREB signaling pathway and block the stimulating effects of ghrelin on GH secretion in the pituitary. Given that these inhibitory effects have been demonstrated in cultured GH-producing cells, they appear to be paracrine and independent of any action on hypothalamic somatostatin release, it would be interesting to analyze whether nesfatins play a role in hypothalamic control of the synthesis and secretion of pituitary GH exerted by SS-GHRH, or on the neurotransmitters involved in this hypothalamic regulation of GH

  • Throughout this review, we have analyzed the effects of three peripheral hormonal factors, ghrelin, klotho, and nesfatins, on pituitary GH synthesis and secretion

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Summary

INTRODUCTION

Our group was the first to describe in humans the existence of an intrinsichypothalamic-somatotrophic rhythm, sexually dimorphic, that conditions the secretion of growth hormone (GH) [1]. It is clear that both hormones play an important role in balancing energy expenditure and metabolic homeostasis Another important hormone, such as cortisol, exerts a positive effect on gastric ghrelin secretion [64], which seems to depend directly on cortisol itself and not on CRH or ACTH, since plasma ghrelin concentrations increase in response to stimulation by ACTH (induced by stress or after exogenous ACTH administration), when metyrapone (which blocks cortisol synthesis) was administered, ACTH increases but plasma ghrelin levels decrease [64]. What is the reason why the secretion of an orexigenic hormone, such as ghrelin, and that of an anabolic hormone, such as GH, is lost with aging?

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