| Literature DB >> 28522826 |
Cécile Pagan1,2,3,4,5,6, Hany Goubran-Botros1,2,7, Richard Delorme1,2,7,3,8, Marion Benabou1,2,7, Nathalie Lemière1,2,7, Kerren Murray1,2,7, Frédérique Amsellem1,3,8, Jacques Callebert4,5, Pauline Chaste1,2,7,3,8, Stéphane Jamain3,9, Fabien Fauchereau1,2,7, Guillaume Huguet1,2,7, Erik Maronde10, Marion Leboyer3,9,11, Jean-Marie Launay12,13,14, Thomas Bourgeron15,16,17,18.
Abstract
Autism spectrum disorders (ASD) are characterized by a wide genetic and clinical heterogeneity. However, some biochemical impairments, including decreased melatonin (crucial for circadian regulation) and elevated platelet N-acetylserotonin (the precursor of melatonin) have been reported as very frequent features in individuals with ASD. To address the mechanisms of these dysfunctions, we investigated melatonin synthesis in post-mortem pineal glands - the main source of melatonin (9 patients and 22 controls) - and gut samples - the main source of serotonin (11 patients and 13 controls), and in blood platelets from 239 individuals with ASD, their first-degree relatives and 278 controls. Our results elucidate the enzymatic mechanism for melatonin deficit in ASD, involving a reduction of both enzyme activities contributing to melatonin synthesis (AANAT and ASMT), observed in the pineal gland as well as in gut and platelets of patients. Further investigations suggest new, post-translational (reduced levels of 14-3-3 proteins which regulate AANAT and ASMT activities) and post-transcriptional (increased levels of miR-451, targeting 14-3-3ζ) mechanisms to these impairments. This study thus gives insights into the pathophysiological pathways involved in ASD.Entities:
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Year: 2017 PMID: 28522826 PMCID: PMC5437096 DOI: 10.1038/s41598-017-02152-x
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379