Adenosine triphosphate inhibits melatonin synthesis in the rat pineal gland. Issue 2 (29th January 2016)

• Record Type: Journal Article
• Authors: Souza‐Teodoro, Luis Henrique; Dargenio‐Garcia, Letícia; Petrilli‐Lapa, Camila Lopes; Souza, Ewerton da Silva; Fernandes, Pedro A. C. M.; Markus, Regina P.; Ferreira, Zulma S.
• Is Part Of: Journal of pineal research. Volume 60:Issue 2(2016)
• Page Start: 242
• Page End: 249
• Publication Date: 2016-01-29
• Subjects: acetylserotonin O‐methyltransferase -- P2Y1 receptors -- pinealocytes -- purinergic signaling; Pineal gland -- Periodicals; Pineal Gland -- Periodicals; Épiphyse (Glande); Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 612.492
• DOI: 10.1111/jpi.12309
• Languages: English
• ISSNs: 0742-3098

Abstract

Abstract: Adenosine triphosphate (ATP) is released onto the pinealocyte, along with noradrenaline, from sympathetic neurons and triggers P2Y1 receptors that enhance β ‐adrenergic‐induced N‐acetylserotonin (NAS) synthesis. Nevertheless, the biotransformation of NAS into melatonin, which occurs due to the subsequent methylation by acetylserotonin O‐methyltransferase (ASMT; EC 2.1.1.4), has not yet been evaluated in the presence of purinergic stimulation. We therefore evaluated the effects of purinergic signaling on melatonin synthesis induced by β ‐adrenergic stimulation. ATP increased NAS levels, but, surprisingly, inhibited melatonin synthesis in an inverse, concentration‐dependent manner. Our results demonstrate that enhanced NAS levels, which depend on phospholipase C (PLC) activity (but not the induction of gene transcription), are a post‐translational effect. By contrast, melatonin reduction is related to an ASMT inhibition of expression at both the gene transcription and protein levels. These results were independent of nuclear factor‐kappa B (NF‐kB) translocation. Neither the P2Y1 receptor activation nor the PLC‐mediated pathway was involved in the decrease in melatonin, indicating that ATP regulates pineal metabolism through different mechanisms. Taken together, our data demonstrate that purinergic signaling differentially modulates NAS and melatonin synthesis and point to a regulatory role for ATP as a cotransmitter in the control of ASMT, the rate‐limiting enzyme in melatonin synthesis. The endogenous production of melatonin regulates defense responses; therefore, understanding the mechanisms involving ASMT regulation might provide novel insights into the development and progression of neurological disorders since melatonin presents anti‐inflammatory, neuroprotective, and neurogenic effects.