Hsuan-Chih N Kuo, Zachary LaRussa, Flora Mengyang Xu, Leslie A Consitt, Min Liu, W Sean Davidson, Vishwajeet Puri, Karen T Coschigano, Haifei Shi, Chunmin C Lo
{"title":"载脂蛋白 A4 可减轻高脂饮食引起的体重增加。","authors":"Hsuan-Chih N Kuo, Zachary LaRussa, Flora Mengyang Xu, Leslie A Consitt, Min Liu, W Sean Davidson, Vishwajeet Puri, Karen T Coschigano, Haifei Shi, Chunmin C Lo","doi":"10.1002/oby.24155","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Apolipoprotein A4 (APOA4) is synthesized by the small intestine in response to dietary lipids. Chronic exposure to a high-fat diet (HFD) desensitizes lipid-induced APOA4 production and attenuates brown adipose tissue (BAT) thermogenesis. We hypothesized that exogenous APOA4 could increase BAT thermogenesis and energy expenditure in HFD-fed mice, resulting in decreased obesity and improved glucose tolerance.</p><p><strong>Methods: </strong>BAT and inguinal white adipose tissue (IWAT) thermogenesis, body composition, energy intake and expenditure, and locomotor activity were measured using an infrared camera, immunoblots, quantitative magnetic resonance imaging, and a comprehensive lab animal monitoring system. An intraperitoneal glucose tolerance test and hepatic lipid accumulation and steatosis were assayed.</p><p><strong>Results: </strong>Mice receiving continuous infusion of APOA4 for the last 4 weeks of 10 weeks of HFD feeding gained no additional body weight and had reduced fat mass but enhanced BAT and IWAT thermogenesis and energy expenditure, despite unaltered food intake and locomotor activity. Additionally, APOA4 infusion elevated fatty acid β oxidation; decreased lipogenesis, lipid accumulation, and steatosis in liver; and improved glucose tolerance.</p><p><strong>Conclusions: </strong>Maintenance of plasma APOA4 via exogenous APOA4 protein parallels elevation of BAT and IWAT thermogenesis, hepatic fatty acid β oxidation, and overall energy expenditure, with subsequent prevention of additional weight gain in HFD-fed obese mice.</p>","PeriodicalId":94163,"journal":{"name":"Obesity (Silver Spring, Md.)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Attenuation of high-fat diet-induced weight gain by apolipoprotein A4.\",\"authors\":\"Hsuan-Chih N Kuo, Zachary LaRussa, Flora Mengyang Xu, Leslie A Consitt, Min Liu, W Sean Davidson, Vishwajeet Puri, Karen T Coschigano, Haifei Shi, Chunmin C Lo\",\"doi\":\"10.1002/oby.24155\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Apolipoprotein A4 (APOA4) is synthesized by the small intestine in response to dietary lipids. Chronic exposure to a high-fat diet (HFD) desensitizes lipid-induced APOA4 production and attenuates brown adipose tissue (BAT) thermogenesis. We hypothesized that exogenous APOA4 could increase BAT thermogenesis and energy expenditure in HFD-fed mice, resulting in decreased obesity and improved glucose tolerance.</p><p><strong>Methods: </strong>BAT and inguinal white adipose tissue (IWAT) thermogenesis, body composition, energy intake and expenditure, and locomotor activity were measured using an infrared camera, immunoblots, quantitative magnetic resonance imaging, and a comprehensive lab animal monitoring system. An intraperitoneal glucose tolerance test and hepatic lipid accumulation and steatosis were assayed.</p><p><strong>Results: </strong>Mice receiving continuous infusion of APOA4 for the last 4 weeks of 10 weeks of HFD feeding gained no additional body weight and had reduced fat mass but enhanced BAT and IWAT thermogenesis and energy expenditure, despite unaltered food intake and locomotor activity. Additionally, APOA4 infusion elevated fatty acid β oxidation; decreased lipogenesis, lipid accumulation, and steatosis in liver; and improved glucose tolerance.</p><p><strong>Conclusions: </strong>Maintenance of plasma APOA4 via exogenous APOA4 protein parallels elevation of BAT and IWAT thermogenesis, hepatic fatty acid β oxidation, and overall energy expenditure, with subsequent prevention of additional weight gain in HFD-fed obese mice.</p>\",\"PeriodicalId\":94163,\"journal\":{\"name\":\"Obesity (Silver Spring, Md.)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Obesity (Silver Spring, Md.)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/oby.24155\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Obesity (Silver Spring, Md.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/oby.24155","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的:载脂蛋白 A4(APOA4)是由小肠对膳食脂质做出反应而合成的。长期暴露于高脂饮食(HFD)会使脂质诱导的 APOA4 生成脱敏,并削弱棕色脂肪组织(BAT)的产热。我们假设外源性 APOA4 可增加高脂饮食小鼠 BAT 的产热和能量消耗,从而减少肥胖并改善葡萄糖耐量:方法:使用红外摄像机、免疫印迹、定量磁共振成像和综合实验动物监测系统测量了BAT和腹股沟白色脂肪组织(IWAT)的产热、身体成分、能量摄入和消耗以及运动活动。此外,还进行了腹腔葡萄糖耐量试验以及肝脏脂质积累和脂肪变性检测:结果:在喂食高纤维食物 10 周的最后 4 周,小鼠持续输注 APOA4,体重没有增加,脂肪量减少,但 BAT 和 IWAT 产热和能量消耗增加,尽管食物摄入量和运动活动没有改变。此外,APOA4输注可提高脂肪酸β氧化;减少脂肪生成、脂质积累和肝脏脂肪变性;改善葡萄糖耐量:结论:通过外源性 APOA4 蛋白维持血浆 APOA4 可提高 BAT 和 IWAT 产热、肝脏脂肪酸 β 氧化和总体能量消耗,从而防止高密度脂蛋白喂养肥胖小鼠体重增加。
Attenuation of high-fat diet-induced weight gain by apolipoprotein A4.
Objective: Apolipoprotein A4 (APOA4) is synthesized by the small intestine in response to dietary lipids. Chronic exposure to a high-fat diet (HFD) desensitizes lipid-induced APOA4 production and attenuates brown adipose tissue (BAT) thermogenesis. We hypothesized that exogenous APOA4 could increase BAT thermogenesis and energy expenditure in HFD-fed mice, resulting in decreased obesity and improved glucose tolerance.
Methods: BAT and inguinal white adipose tissue (IWAT) thermogenesis, body composition, energy intake and expenditure, and locomotor activity were measured using an infrared camera, immunoblots, quantitative magnetic resonance imaging, and a comprehensive lab animal monitoring system. An intraperitoneal glucose tolerance test and hepatic lipid accumulation and steatosis were assayed.
Results: Mice receiving continuous infusion of APOA4 for the last 4 weeks of 10 weeks of HFD feeding gained no additional body weight and had reduced fat mass but enhanced BAT and IWAT thermogenesis and energy expenditure, despite unaltered food intake and locomotor activity. Additionally, APOA4 infusion elevated fatty acid β oxidation; decreased lipogenesis, lipid accumulation, and steatosis in liver; and improved glucose tolerance.
Conclusions: Maintenance of plasma APOA4 via exogenous APOA4 protein parallels elevation of BAT and IWAT thermogenesis, hepatic fatty acid β oxidation, and overall energy expenditure, with subsequent prevention of additional weight gain in HFD-fed obese mice.