Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H 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...
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Public Library of Science (PLoS)
2013-01-01
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Online Access: | http://europepmc.org/articles/PMC3789719?pdf=render |
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author | Eun-Young Won Mi-Kyung Yoon Sang-Woo Kim Youngae Jung Hyun-Whee Bae Daeyoup Lee Sung Goo Park Chul-Ho Lee Geum-Sook Hwang Seung-Wook Chi |
author_facet | Eun-Young Won Mi-Kyung Yoon Sang-Woo Kim Youngae Jung Hyun-Whee Bae Daeyoup Lee Sung Goo Park Chul-Ho Lee Geum-Sook Hwang Seung-Wook Chi |
author_sort | Eun-Young Won |
collection | DOAJ |
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. |
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institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-11T18:22:00Z |
publishDate | 2013-01-01 |
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spelling | doaj.art-ecec787d5be64224bbe10c0d052a35062022-12-22T00:55:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01810e7599810.1371/journal.pone.0075998Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy.Eun-Young WonMi-Kyung YoonSang-Woo KimYoungae JungHyun-Whee BaeDaeyoup LeeSung Goo ParkChul-Ho LeeGeum-Sook HwangSeung-Wook ChiDespite 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.http://europepmc.org/articles/PMC3789719?pdf=render |
spellingShingle | Eun-Young Won Mi-Kyung Yoon Sang-Woo Kim Youngae Jung Hyun-Whee Bae Daeyoup Lee Sung Goo Park Chul-Ho Lee Geum-Sook Hwang Seung-Wook Chi Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy. PLoS ONE |
title | Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy. |
title_full | Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy. |
title_fullStr | Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy. |
title_full_unstemmed | Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy. |
title_short | Gender-specific metabolomic profiling of obesity in leptin-deficient ob/ob mice by 1H NMR spectroscopy. |
title_sort | gender specific metabolomic profiling of obesity in leptin deficient ob ob mice by 1h nmr spectroscopy |
url | http://europepmc.org/articles/PMC3789719?pdf=render |
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