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Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy
Despite the numerous metabolic studies on obesity, gender bias in obesity has rarely been investigated. Here, we report the metabolomic analysis of obesity by using leptin-deficient ob/ob mice based on the gender. Metabolomic analyses of urine and serum from ob/ob mice compared with those from C57BL...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789719/ https://www.ncbi.nlm.nih.gov/pubmed/24098417 http://dx.doi.org/10.1371/journal.pone.0075998 |
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author | Won, Eun-Young Yoon, Mi-Kyung Kim, Sang-Woo Jung, Youngae Bae, Hyun-Whee Lee, Daeyoup Park, Sung Goo Lee, Chul-Ho Hwang, Geum-Sook Chi, Seung-Wook |
author_facet | Won, Eun-Young Yoon, Mi-Kyung Kim, Sang-Woo Jung, Youngae Bae, Hyun-Whee Lee, Daeyoup Park, Sung Goo Lee, Chul-Ho Hwang, Geum-Sook Chi, Seung-Wook |
author_sort | Won, Eun-Young |
collection | PubMed |
description | Despite the numerous metabolic studies on obesity, gender bias in obesity has rarely been investigated. Here, we report the metabolomic analysis of obesity by using leptin-deficient ob/ob mice based on the gender. Metabolomic analyses of urine and serum from ob/ob mice compared with those from C57BL/6J lean mice, based on the (1)H NMR spectroscopy in combination with multivariate statistical analysis, revealed clear metabolic differences between obese and lean mice. We also identified 48 urine and 22 serum metabolites that were statistically significantly altered in obese mice compared to lean controls. These metabolites are involved in amino acid metabolism (leucine, alanine, ariginine, lysine, and methionine), tricarbocylic acid cycle and glucose metabolism (pyruvate, citrate, glycolate, acetoacetate, and acetone), lipid metabolism (cholesterol and carnitine), creatine metabolism (creatine and creatinine), and gut-microbiome-derived metabolism (choline, TMAO, hippurate, p-cresol, isobutyrate, 2-hydroxyisobutyrate, methylamine, and trigonelline). Notably, our metabolomic studies showed distinct gender variations. The obese male mice metabolism was specifically associated with insulin signaling, whereas the obese female mice metabolism was associated with lipid metabolism. Taken together, our study identifies the biomarker signature for obesity in ob/ob mice and provides biochemical insights into the metabolic alteration in obesity based on gender. |
format | Online Article Text |
id | pubmed-3789719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37897192013-10-04 Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy Won, Eun-Young Yoon, Mi-Kyung Kim, Sang-Woo Jung, Youngae Bae, Hyun-Whee Lee, Daeyoup Park, Sung Goo Lee, Chul-Ho Hwang, Geum-Sook Chi, Seung-Wook PLoS One Research Article Despite the numerous metabolic studies on obesity, gender bias in obesity has rarely been investigated. Here, we report the metabolomic analysis of obesity by using leptin-deficient ob/ob mice based on the gender. Metabolomic analyses of urine and serum from ob/ob mice compared with those from C57BL/6J lean mice, based on the (1)H NMR spectroscopy in combination with multivariate statistical analysis, revealed clear metabolic differences between obese and lean mice. We also identified 48 urine and 22 serum metabolites that were statistically significantly altered in obese mice compared to lean controls. These metabolites are involved in amino acid metabolism (leucine, alanine, ariginine, lysine, and methionine), tricarbocylic acid cycle and glucose metabolism (pyruvate, citrate, glycolate, acetoacetate, and acetone), lipid metabolism (cholesterol and carnitine), creatine metabolism (creatine and creatinine), and gut-microbiome-derived metabolism (choline, TMAO, hippurate, p-cresol, isobutyrate, 2-hydroxyisobutyrate, methylamine, and trigonelline). Notably, our metabolomic studies showed distinct gender variations. The obese male mice metabolism was specifically associated with insulin signaling, whereas the obese female mice metabolism was associated with lipid metabolism. Taken together, our study identifies the biomarker signature for obesity in ob/ob mice and provides biochemical insights into the metabolic alteration in obesity based on gender. Public Library of Science 2013-10-03 /pmc/articles/PMC3789719/ /pubmed/24098417 http://dx.doi.org/10.1371/journal.pone.0075998 Text en © 2013 Won 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 Won, Eun-Young Yoon, Mi-Kyung Kim, Sang-Woo Jung, Youngae Bae, Hyun-Whee Lee, Daeyoup Park, Sung Goo Lee, Chul-Ho Hwang, Geum-Sook Chi, Seung-Wook Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy |
title | Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy |
title_full | Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy |
title_fullStr | Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy |
title_full_unstemmed | Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy |
title_short | Gender-Specific Metabolomic Profiling of Obesity in Leptin-Deficient ob/ob Mice by (1)H NMR Spectroscopy |
title_sort | gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by (1)h nmr spectroscopy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789719/ https://www.ncbi.nlm.nih.gov/pubmed/24098417 http://dx.doi.org/10.1371/journal.pone.0075998 |
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