{"title":"Individual differences in response to a chronic high-fat diet in striped hamsters (Cricetulus barabensis)","authors":"Wenting Li , Binxin Yin , Xinyuan Dong , Boyang Ding , Jing Wen","doi":"10.1016/j.cbpa.2025.111896","DOIUrl":null,"url":null,"abstract":"<div><div>Adult male striped hamsters (<em>Cricetulus barabensis</em>) were fed an HFD for 12 weeks to examine individual differences in response to chronic exposure to a high-fat diet (HFD). The hamsters were subsequently assigned to three experimental groups according to those that exhibited body weight gain (GW), a stable body weight (SW), or body weight loss (LW). The GW group showed a profile of HFD-induced obesity, with the highest levels of energy intake, fat content, brown adipose tissue (BAT) mass, <em>UCP1</em> gene expression in the BAT, and lipid metabolism. The SW group was resistant to HFD, showing lower levels of the above-mentioned markers than those of the GW group. In addition, the LW group appeared to be aversive to HFD, displaying a negative body mass gain compared to the other two groups. Group differences in the relative abundance of several strains of the gut microbiota were also observed, suggesting the potential involvement of the gut microbiota in individual variation in the sensitivity, resistance, and aversive responses to HFD-induced obesity. These data demonstrate the utility of the striped hamster model in functional studies of the mechanisms underlying HFD-induced obesity and its potential treatment and prevention.</div></div>","PeriodicalId":55237,"journal":{"name":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","volume":"307 ","pages":"Article 111896"},"PeriodicalIF":2.1000,"publicationDate":"2025-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1095643325000959","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Adult male striped hamsters (Cricetulus barabensis) were fed an HFD for 12 weeks to examine individual differences in response to chronic exposure to a high-fat diet (HFD). The hamsters were subsequently assigned to three experimental groups according to those that exhibited body weight gain (GW), a stable body weight (SW), or body weight loss (LW). The GW group showed a profile of HFD-induced obesity, with the highest levels of energy intake, fat content, brown adipose tissue (BAT) mass, UCP1 gene expression in the BAT, and lipid metabolism. The SW group was resistant to HFD, showing lower levels of the above-mentioned markers than those of the GW group. In addition, the LW group appeared to be aversive to HFD, displaying a negative body mass gain compared to the other two groups. Group differences in the relative abundance of several strains of the gut microbiota were also observed, suggesting the potential involvement of the gut microbiota in individual variation in the sensitivity, resistance, and aversive responses to HFD-induced obesity. These data demonstrate the utility of the striped hamster model in functional studies of the mechanisms underlying HFD-induced obesity and its potential treatment and prevention.
期刊介绍:
Part A: Molecular & Integrative Physiology of Comparative Biochemistry and Physiology. This journal covers molecular, cellular, integrative, and ecological physiology. Topics include bioenergetics, circulation, development, excretion, ion regulation, endocrinology, neurobiology, nutrition, respiration, and thermal biology. Study on regulatory mechanisms at any level of organization such as signal transduction and cellular interaction and control of behavior are also published.