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Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective

Melatonin is an endogenously produced indoleamine and secreted by the pineal gland. Melatonin has pleiotropic bioactivities and is involved in epigenetic regulation. Suboptimal conditions during maternal and perinatal phases can elicit epigenetic regulation of genes for nephrogenesis and reset physi...

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Detalles Bibliográficos
Autores principales: Tain, You-Lin, Huang, Li-Tung, Chan, Julie Y. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227227/
https://www.ncbi.nlm.nih.gov/pubmed/25318052
http://dx.doi.org/10.3390/ijms151018484
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author Tain, You-Lin
Huang, Li-Tung
Chan, Julie Y. H.
author_facet Tain, You-Lin
Huang, Li-Tung
Chan, Julie Y. H.
author_sort Tain, You-Lin
collection PubMed
description Melatonin is an endogenously produced indoleamine and secreted by the pineal gland. Melatonin has pleiotropic bioactivities and is involved in epigenetic regulation. Suboptimal conditions during maternal and perinatal phases can elicit epigenetic regulation of genes for nephrogenesis and reset physiological responses to develop programmed hypertension. This review discusses the early utility of melatonin to prevent programmed hypertension in later life by epigenetic regulation in the kidney, with an emphasis on: (1) the role of melatonin in epigenetic regulation; (2) the beneficial effects of melatonin on programmed hypertension; (3) epigenetic regulation of maternal melatonin therapy in different developmental windows of offspring kidneys analyzed by whole-genome RNA next-generation sequencing; and (4) current blocks in the application of melatonin in preventing programmed hypertension.
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spelling pubmed-42272272014-11-12 Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective Tain, You-Lin Huang, Li-Tung Chan, Julie Y. H. Int J Mol Sci Review Melatonin is an endogenously produced indoleamine and secreted by the pineal gland. Melatonin has pleiotropic bioactivities and is involved in epigenetic regulation. Suboptimal conditions during maternal and perinatal phases can elicit epigenetic regulation of genes for nephrogenesis and reset physiological responses to develop programmed hypertension. This review discusses the early utility of melatonin to prevent programmed hypertension in later life by epigenetic regulation in the kidney, with an emphasis on: (1) the role of melatonin in epigenetic regulation; (2) the beneficial effects of melatonin on programmed hypertension; (3) epigenetic regulation of maternal melatonin therapy in different developmental windows of offspring kidneys analyzed by whole-genome RNA next-generation sequencing; and (4) current blocks in the application of melatonin in preventing programmed hypertension. MDPI 2014-10-14 /pmc/articles/PMC4227227/ /pubmed/25318052 http://dx.doi.org/10.3390/ijms151018484 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tain, You-Lin
Huang, Li-Tung
Chan, Julie Y. H.
Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective
title Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective
title_full Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective
title_fullStr Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective
title_full_unstemmed Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective
title_short Transcriptional Regulation of Programmed Hypertension by Melatonin: An Epigenetic Perspective
title_sort transcriptional regulation of programmed hypertension by melatonin: an epigenetic perspective
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227227/
https://www.ncbi.nlm.nih.gov/pubmed/25318052
http://dx.doi.org/10.3390/ijms151018484
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