2010
DOI: 10.1002/pmic.201000391
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Plasma proteome analysis in diet‐induced obesity‐prone and obesity‐resistant rats

Abstract: One of the major issues in the field of obesity is why some humans become obese and others resist development of obesity when exposed to high-calorie diets. Despite the same genetic background, namely obesity-prone (OP) and -resistant (OR) rats, differing responses have been demonstrated in a high fat diet-induced rodent model. The aim of the present study was to discover novel obesity-related biomarkers for susceptibility and/or resistance to obesity by proteomic analysis of OP and OR rat plasma. After feedin… Show more

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Cited by 32 publications
(28 citation statements)
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“…In our previous studies, we found that male rats are more susceptible to obesity when fed a HFD, and many proteins play roles in obesity resistance in different metabolic tissues [13][16]. In conjunction with the present data, an earlier report demonstrated the anti-obesity effects of CAV1, as evidenced by reduced Cav1 expression in visceral adipose tissue of obese patients [10].…”
Section: Introductionsupporting
confidence: 89%
“…In our previous studies, we found that male rats are more susceptible to obesity when fed a HFD, and many proteins play roles in obesity resistance in different metabolic tissues [13][16]. In conjunction with the present data, an earlier report demonstrated the anti-obesity effects of CAV1, as evidenced by reduced Cav1 expression in visceral adipose tissue of obese patients [10].…”
Section: Introductionsupporting
confidence: 89%
“…Microarray analysis revealed differences in expression of genes encoding metabolic enzymes in adipose tissue from OP and OR rats (13). Plasma proteome analysis showed changes related to inflammation and oxidative stress (14). We confirmed accelerated weight gain, increased adiposity, and altered metabolic parameters in OP rats.…”
Section: Discussionsupporting
confidence: 62%
“…Of the 16 differentially expressed proteins identified in this study, 14 have already been associated with other chronic diseases in rats [28], humans [18-22,24,29,30], and horses [26] using DIGE. To our knowledge, coagulation factor X and IgA have not been associated with either acute or chronic diseases using DIGE based proteomics.…”
Section: Discussionmentioning
confidence: 99%