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Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation

BACKGROUND: Adipose tissue patterning has a major influence on the risk of developing chronic disease. Environmental influences on both body fat patterning and appetite regulation are not fully understood. This study was performed to investigate the impact of resistant starch (RS) on adipose tissue...

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Autores principales: So, Po-Wah, Yu, Wei-Sheng, Kuo, Yu-Ting, Wasserfall, Clive, Goldstone, Anthony P., Bell, Jimmy D., Frost, Gary
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111051/
https://www.ncbi.nlm.nih.gov/pubmed/18074032
http://dx.doi.org/10.1371/journal.pone.0001309
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author So, Po-Wah
Yu, Wei-Sheng
Kuo, Yu-Ting
Wasserfall, Clive
Goldstone, Anthony P.
Bell, Jimmy D.
Frost, Gary
author_facet So, Po-Wah
Yu, Wei-Sheng
Kuo, Yu-Ting
Wasserfall, Clive
Goldstone, Anthony P.
Bell, Jimmy D.
Frost, Gary
author_sort So, Po-Wah
collection PubMed
description BACKGROUND: Adipose tissue patterning has a major influence on the risk of developing chronic disease. Environmental influences on both body fat patterning and appetite regulation are not fully understood. This study was performed to investigate the impact of resistant starch (RS) on adipose tissue deposition and central regulation of appetite in mice. METHODOLOGY AND PRINCIPLE FINDINGS: Forty mice were randomised to a diet supplemented with either the high resistant starch (HRS), or the readily digestible starch (LRS). Using (1)H magnetic resonance (MR) methods, whole body adiposity, intrahepatocellular lipids (IHCL) and intramyocellular lipids (IMCL) were measured. Manganese-enhanced MRI (MEMRI) was used to investigate neuronal activity in hypothalamic regions involved in appetite control when fed ad libitum. At the end of the interventional period, adipocytes were isolated from epididymal adipose tissue and fasting plasma collected for hormonal and adipokine measurement. Mice on the HRS and LRS diet had similar body weights although total body adiposity, subcutaneous and visceral fat, IHCL, plasma leptin, plasma adiponectin plasma insulin/glucose ratios was significantly greater in the latter group. Adipocytes isolated from the LRS group were significantly larger and had lower insulin-stimulated glucose uptake. MEMRI data obtained from the ventromedial and paraventricular hypothalamic nuclei suggests a satiating effect of the HRS diet despite a lower energy intake. CONCLUSION AND SIGNIFICANCE: Dietary RS significantly impacts on adipose tissue patterning, adipocyte morphology and metabolism, glucose and insulin metabolism, as well as affecting appetite regulation, supported by changes in neuronal activity in hypothalamic appetite regulation centres which are suggestive of satiation.
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spelling pubmed-21110512007-12-12 Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation So, Po-Wah Yu, Wei-Sheng Kuo, Yu-Ting Wasserfall, Clive Goldstone, Anthony P. Bell, Jimmy D. Frost, Gary PLoS One Research Article BACKGROUND: Adipose tissue patterning has a major influence on the risk of developing chronic disease. Environmental influences on both body fat patterning and appetite regulation are not fully understood. This study was performed to investigate the impact of resistant starch (RS) on adipose tissue deposition and central regulation of appetite in mice. METHODOLOGY AND PRINCIPLE FINDINGS: Forty mice were randomised to a diet supplemented with either the high resistant starch (HRS), or the readily digestible starch (LRS). Using (1)H magnetic resonance (MR) methods, whole body adiposity, intrahepatocellular lipids (IHCL) and intramyocellular lipids (IMCL) were measured. Manganese-enhanced MRI (MEMRI) was used to investigate neuronal activity in hypothalamic regions involved in appetite control when fed ad libitum. At the end of the interventional period, adipocytes were isolated from epididymal adipose tissue and fasting plasma collected for hormonal and adipokine measurement. Mice on the HRS and LRS diet had similar body weights although total body adiposity, subcutaneous and visceral fat, IHCL, plasma leptin, plasma adiponectin plasma insulin/glucose ratios was significantly greater in the latter group. Adipocytes isolated from the LRS group were significantly larger and had lower insulin-stimulated glucose uptake. MEMRI data obtained from the ventromedial and paraventricular hypothalamic nuclei suggests a satiating effect of the HRS diet despite a lower energy intake. CONCLUSION AND SIGNIFICANCE: Dietary RS significantly impacts on adipose tissue patterning, adipocyte morphology and metabolism, glucose and insulin metabolism, as well as affecting appetite regulation, supported by changes in neuronal activity in hypothalamic appetite regulation centres which are suggestive of satiation. Public Library of Science 2007-12-12 /pmc/articles/PMC2111051/ /pubmed/18074032 http://dx.doi.org/10.1371/journal.pone.0001309 Text en So et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
So, Po-Wah
Yu, Wei-Sheng
Kuo, Yu-Ting
Wasserfall, Clive
Goldstone, Anthony P.
Bell, Jimmy D.
Frost, Gary
Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation
title Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation
title_full Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation
title_fullStr Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation
title_full_unstemmed Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation
title_short Impact of Resistant Starch on Body Fat Patterning and Central Appetite Regulation
title_sort impact of resistant starch on body fat patterning and central appetite regulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111051/
https://www.ncbi.nlm.nih.gov/pubmed/18074032
http://dx.doi.org/10.1371/journal.pone.0001309
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