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Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring

BACKGROUND: Intrauterine growth retardation due to maternal under-nutrition increases susceptibility to obesity and insulin resistance. We reported earlier in the offspring of mineral or vitamin restricted rat dams, a high body fat percentage and decreased insulin secretion to glucose challenge. Thi...

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Autores principales: Lagishetty, Venu, Nandiwada, Vijaya Bhanu, Kalashikam, Rajender Rao, Manchala, Raghunath
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2098757/
https://www.ncbi.nlm.nih.gov/pubmed/17937812
http://dx.doi.org/10.1186/1743-7075-4-21
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author Lagishetty, Venu
Nandiwada, Vijaya Bhanu
Kalashikam, Rajender Rao
Manchala, Raghunath
author_facet Lagishetty, Venu
Nandiwada, Vijaya Bhanu
Kalashikam, Rajender Rao
Manchala, Raghunath
author_sort Lagishetty, Venu
collection PubMed
description BACKGROUND: Intrauterine growth retardation due to maternal under-nutrition increases susceptibility to obesity and insulin resistance. We reported earlier in the offspring of mineral or vitamin restricted rat dams, a high body fat percentage and decreased insulin secretion to glucose challenge. This study determined whether or not central adiposity and altered adipocytokine profile were associated with high body fat content. METHODS: Body fat percentage; glucose, insulin and adipocytokine levels in fasting plasma and fresh weights of epididymal fat pads were determined in the six months old male offspring of Wistar NIN rat dams on chronic 50 percent restriction of vitamins or minerals throughout their growth, gestation, lactation and weaned on to restricted diets or restricted mothers/offspring rehabilitated from different time points. RESULTS: In line with high body fat percent, chronic restriction of vitamins and minerals increased the epididymal fat pad weight. Maternal vitamin restriction decreased plasma adiponectin and increased leptin levels whereas mineral restriction decreased both. Both the treatments did not affect plasma TNF-α levels or insulin resistance status (HOMA-IR). Rehabilitation from parturition but not weaning, rescued the changes in the offspring. CONCLUSION: High body fat percentage in the offspring of vitamin restricted or mineral restricted rat dams was associated with increased abdominal adiposity (epididymal fat pad weight) and differential expression of adipocytokines but not insulin resistance. The changes could be mitigated by rehabilitation from birth but not weaning.
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spelling pubmed-20987572007-11-29 Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring Lagishetty, Venu Nandiwada, Vijaya Bhanu Kalashikam, Rajender Rao Manchala, Raghunath Nutr Metab (Lond) Brief Communication BACKGROUND: Intrauterine growth retardation due to maternal under-nutrition increases susceptibility to obesity and insulin resistance. We reported earlier in the offspring of mineral or vitamin restricted rat dams, a high body fat percentage and decreased insulin secretion to glucose challenge. This study determined whether or not central adiposity and altered adipocytokine profile were associated with high body fat content. METHODS: Body fat percentage; glucose, insulin and adipocytokine levels in fasting plasma and fresh weights of epididymal fat pads were determined in the six months old male offspring of Wistar NIN rat dams on chronic 50 percent restriction of vitamins or minerals throughout their growth, gestation, lactation and weaned on to restricted diets or restricted mothers/offspring rehabilitated from different time points. RESULTS: In line with high body fat percent, chronic restriction of vitamins and minerals increased the epididymal fat pad weight. Maternal vitamin restriction decreased plasma adiponectin and increased leptin levels whereas mineral restriction decreased both. Both the treatments did not affect plasma TNF-α levels or insulin resistance status (HOMA-IR). Rehabilitation from parturition but not weaning, rescued the changes in the offspring. CONCLUSION: High body fat percentage in the offspring of vitamin restricted or mineral restricted rat dams was associated with increased abdominal adiposity (epididymal fat pad weight) and differential expression of adipocytokines but not insulin resistance. The changes could be mitigated by rehabilitation from birth but not weaning. BioMed Central 2007-10-15 /pmc/articles/PMC2098757/ /pubmed/17937812 http://dx.doi.org/10.1186/1743-7075-4-21 Text en Copyright © 2007 Lagishetty et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Lagishetty, Venu
Nandiwada, Vijaya Bhanu
Kalashikam, Rajender Rao
Manchala, Raghunath
Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring
title Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring
title_full Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring
title_fullStr Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring
title_full_unstemmed Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring
title_short Effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of WNIN rat offspring
title_sort effect of maternal vitamin and mineral restrictions on the body fat content and adipocytokine levels of wnin rat offspring
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2098757/
https://www.ncbi.nlm.nih.gov/pubmed/17937812
http://dx.doi.org/10.1186/1743-7075-4-21
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