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Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management

Recent advances in molecular biology combined with the wealth of information generated by the Human Genome Project have fostered the emergence of nutrigenomics, a new discipline in the field of nutritional research. Nutrigenomics may provide the strategies for the development of safe and effective d...

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Detalles Bibliográficos
Autores principales: Lau, Francis C, Bagchi, Manashi, Sen, Chandan, Roy, Sashwati, Bagchi, Debasis
Formato: Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2682937/
https://www.ncbi.nlm.nih.gov/pubmed/19452041
http://dx.doi.org/10.2174/138920208784533638
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author Lau, Francis C
Bagchi, Manashi
Sen, Chandan
Roy, Sashwati
Bagchi, Debasis
author_facet Lau, Francis C
Bagchi, Manashi
Sen, Chandan
Roy, Sashwati
Bagchi, Debasis
author_sort Lau, Francis C
collection PubMed
description Recent advances in molecular biology combined with the wealth of information generated by the Human Genome Project have fostered the emergence of nutrigenomics, a new discipline in the field of nutritional research. Nutrigenomics may provide the strategies for the development of safe and effective dietary interventions against the obesity epidemic. According to the World Health Organization, more than 60% of the global disease burden will be attributed to chronic disorders associated with obesity by 2020. Meanwhile in the US, the prevalence of obesity has doubled in adults and tripled in children during the past three decades. In this regard, a number of natural dietary supplements and micronutrients have been studied for their potential in weight management. Among these supplements, (–)-hydroxycitric acid (HCA), a natural extract isolated from the dried fruit rind of Garcinia cambogia, and the micronutrient niacin-bound chromium(III) (NBC) have been shown to be safe and efficacious for weight loss. Utilizing cDNA microarrays, we demonstrated for the first time that HCA-supplementation altered the expression of genes involved in lipolytic and adipogenic pathways in adipocytes from obese women and up-regulated the expression of serotonin receptor gene in the abdominal fat of rats. Similarly, we showed that NBC-supplementation up-regulated the expression of myogenic genes while suppressed the expression of genes that are highly expressed in brown adipose tissue in diabetic obese mice. The potential biological mechanisms underlying the observed beneficial effects of these supplements as elucidated by the state-of-the-art nutrigenomic technologies will be systematically discussed in this review.
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spelling pubmed-26829372009-05-18 Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management Lau, Francis C Bagchi, Manashi Sen, Chandan Roy, Sashwati Bagchi, Debasis Curr Genomics Article Recent advances in molecular biology combined with the wealth of information generated by the Human Genome Project have fostered the emergence of nutrigenomics, a new discipline in the field of nutritional research. Nutrigenomics may provide the strategies for the development of safe and effective dietary interventions against the obesity epidemic. According to the World Health Organization, more than 60% of the global disease burden will be attributed to chronic disorders associated with obesity by 2020. Meanwhile in the US, the prevalence of obesity has doubled in adults and tripled in children during the past three decades. In this regard, a number of natural dietary supplements and micronutrients have been studied for their potential in weight management. Among these supplements, (–)-hydroxycitric acid (HCA), a natural extract isolated from the dried fruit rind of Garcinia cambogia, and the micronutrient niacin-bound chromium(III) (NBC) have been shown to be safe and efficacious for weight loss. Utilizing cDNA microarrays, we demonstrated for the first time that HCA-supplementation altered the expression of genes involved in lipolytic and adipogenic pathways in adipocytes from obese women and up-regulated the expression of serotonin receptor gene in the abdominal fat of rats. Similarly, we showed that NBC-supplementation up-regulated the expression of myogenic genes while suppressed the expression of genes that are highly expressed in brown adipose tissue in diabetic obese mice. The potential biological mechanisms underlying the observed beneficial effects of these supplements as elucidated by the state-of-the-art nutrigenomic technologies will be systematically discussed in this review. Bentham Science Publishers Ltd. 2008-06 /pmc/articles/PMC2682937/ /pubmed/19452041 http://dx.doi.org/10.2174/138920208784533638 Text en ©2008 Bentham Science Publishers Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/) which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Lau, Francis C
Bagchi, Manashi
Sen, Chandan
Roy, Sashwati
Bagchi, Debasis
Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management
title Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management
title_full Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management
title_fullStr Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management
title_full_unstemmed Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management
title_short Nutrigenomic Analysis of Diet-Gene Interactions on Functional Supplements for Weight Management
title_sort nutrigenomic analysis of diet-gene interactions on functional supplements for weight management
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2682937/
https://www.ncbi.nlm.nih.gov/pubmed/19452041
http://dx.doi.org/10.2174/138920208784533638
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