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Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet
Obesity is one of the major global health problems. Melatonin deficiency has been demonstrated to correlate with obesity. The aim of the study was to estimate the effect of melatonin on oxidative stress and adipokine levels in obese patients on a calorie-restricted diet. Thirty obese patients were s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632922/ https://www.ncbi.nlm.nih.gov/pubmed/29142618 http://dx.doi.org/10.1155/2017/8494107 |
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author | Szewczyk-Golec, Karolina Rajewski, Paweł Gackowski, Marcin Mila-Kierzenkowska, Celestyna Wesołowski, Roland Sutkowy, Paweł Pawłowska, Marta Woźniak, Alina |
author_facet | Szewczyk-Golec, Karolina Rajewski, Paweł Gackowski, Marcin Mila-Kierzenkowska, Celestyna Wesołowski, Roland Sutkowy, Paweł Pawłowska, Marta Woźniak, Alina |
author_sort | Szewczyk-Golec, Karolina |
collection | PubMed |
description | Obesity is one of the major global health problems. Melatonin deficiency has been demonstrated to correlate with obesity. The aim of the study was to estimate the effect of melatonin on oxidative stress and adipokine levels in obese patients on a calorie-restricted diet. Thirty obese patients were supplemented with a daily dose of 10 mg of melatonin (n = 15) or placebo (n = 15) for 30 days with a calorie-restricted diet. Serum levels of melatonin, 4-hydroxynonenal (HNE), adiponectin, omentin-1, leptin, and resistin, as well as erythrocytic malondialdehyde (MDA) concentration and Zn/Cu-superoxide dismutase, catalase, and glutathione peroxidase (GPx) activities, were measured at baseline and after supplementation. Significant body weight reduction was observed only in the melatonin group. After melatonin supplementation, the adiponectin and omentin-1 levels and GPx activities statistically increased, whereas the MDA concentrations were reduced. In the placebo group, a significant rise in the HNE and a drop in the melatonin concentrations were found. The results show evidence of increased oxidative stress accompanying calorie restriction. Melatonin supplementation facilitated body weight reduction, improved the antioxidant defense, and regulated adipokine secretion. The findings strongly suggest that melatonin should be considered in obesity management. This trial is registered with CTRI/2017/07/009093. |
format | Online Article Text |
id | pubmed-5632922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56329222017-11-15 Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet Szewczyk-Golec, Karolina Rajewski, Paweł Gackowski, Marcin Mila-Kierzenkowska, Celestyna Wesołowski, Roland Sutkowy, Paweł Pawłowska, Marta Woźniak, Alina Oxid Med Cell Longev Research Article Obesity is one of the major global health problems. Melatonin deficiency has been demonstrated to correlate with obesity. The aim of the study was to estimate the effect of melatonin on oxidative stress and adipokine levels in obese patients on a calorie-restricted diet. Thirty obese patients were supplemented with a daily dose of 10 mg of melatonin (n = 15) or placebo (n = 15) for 30 days with a calorie-restricted diet. Serum levels of melatonin, 4-hydroxynonenal (HNE), adiponectin, omentin-1, leptin, and resistin, as well as erythrocytic malondialdehyde (MDA) concentration and Zn/Cu-superoxide dismutase, catalase, and glutathione peroxidase (GPx) activities, were measured at baseline and after supplementation. Significant body weight reduction was observed only in the melatonin group. After melatonin supplementation, the adiponectin and omentin-1 levels and GPx activities statistically increased, whereas the MDA concentrations were reduced. In the placebo group, a significant rise in the HNE and a drop in the melatonin concentrations were found. The results show evidence of increased oxidative stress accompanying calorie restriction. Melatonin supplementation facilitated body weight reduction, improved the antioxidant defense, and regulated adipokine secretion. The findings strongly suggest that melatonin should be considered in obesity management. This trial is registered with CTRI/2017/07/009093. Hindawi 2017 2017-09-21 /pmc/articles/PMC5632922/ /pubmed/29142618 http://dx.doi.org/10.1155/2017/8494107 Text en Copyright © 2017 Karolina Szewczyk-Golec et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Szewczyk-Golec, Karolina Rajewski, Paweł Gackowski, Marcin Mila-Kierzenkowska, Celestyna Wesołowski, Roland Sutkowy, Paweł Pawłowska, Marta Woźniak, Alina Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet |
title | Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet |
title_full | Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet |
title_fullStr | Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet |
title_full_unstemmed | Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet |
title_short | Melatonin Supplementation Lowers Oxidative Stress and Regulates Adipokines in Obese Patients on a Calorie-Restricted Diet |
title_sort | melatonin supplementation lowers oxidative stress and regulates adipokines in obese patients on a calorie-restricted diet |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632922/ https://www.ncbi.nlm.nih.gov/pubmed/29142618 http://dx.doi.org/10.1155/2017/8494107 |
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