Mentzel Caroline M Junker, Cardoso Tainã Figueiredo, Lex Annika M J, Sørensen Dorte Bratbo, Fredholm Merete, Cirera Susanna
Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg, Denmark.
Department of Animal Genetics, Center for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Mamm Genome. 2017 Jun;28(5-6):166-175. doi: 10.1007/s00335-017-9690-y. Epub 2017 Apr 10.
In human health, there is interest in developing specific diets to reduce body weight. These studies are mainly focused on phenotypic changes induced in blood measurements, i.e., triglycerides, HDL, LDL, and insulin, and on physical changes, i.e., body weight and BMI. To evaluate the biological impact of diet interventions, it is very important to investigate the molecular mechanisms driving the diet-induced phenotypic changes in relevant tissues. However, studying these effects in humans is difficult due to ethical concerns in doing interventions and obtaining tissue samples and good animal models are therefore needed. Göttingen minipigs, a small size obesity prone pig breed, have previously been shown to be a useful translational animal model for metabolic studies. In this study, 16 Göttingen minipig males (2-month old) were submitted to 13 weeks of differential diets to investigate the initial stages of diet-induced metabolic changes. Half of them were fed a high-fat/cholesterol, low-carbohydrate (HFLC) diet, and the other half were fed a low- fat/cholesterol, high-carbohydrate (LFHC) diet. After 13 weeks, the HFLC group weighted less and had dyslipidemia compared to the LFHC group. Liver, pancreas, and adipose tissues were collected at slaughter. Gene expression profiling of 83 metabolism-relevant genes was performed using high-throughput qPCR. In total, 41 genes were deregulated in at least one of the five tissues analyzed, with liver being the most drastically affected tissue. The new knowledge gained in this study could potentially be of value for considering direct modulation of gene expression by nutrient content in the diet.
在人类健康领域,人们对开发特定饮食以减轻体重很感兴趣。这些研究主要集中在血液检测指标(即甘油三酯、高密度脂蛋白、低密度脂蛋白和胰岛素)所诱导的表型变化,以及身体变化(即体重和身体质量指数)上。为了评估饮食干预的生物学影响,研究相关组织中驱动饮食诱导表型变化的分子机制非常重要。然而,由于进行干预和获取组织样本存在伦理问题,在人类中研究这些影响很困难,因此需要良好的动物模型。哥廷根小型猪是一种易于肥胖的小型猪品种,先前已被证明是代谢研究中一种有用的转化动物模型。在本研究中,16只2月龄的雄性哥廷根小型猪接受了13周的不同饮食,以研究饮食诱导的代谢变化的初始阶段。其中一半喂食高脂肪/高胆固醇、低碳水化合物(HFLC)饮食,另一半喂食低脂肪/低胆固醇、高碳水化合物(LFHC)饮食。13周后,与LFHC组相比,HFLC组体重更轻且存在血脂异常。屠宰时收集肝脏、胰腺和脂肪组织。使用高通量定量PCR对83个与代谢相关的基因进行基因表达谱分析。总共,在分析的五个组织中的至少一个组织中,有41个基因的表达失调,其中肝脏是受影响最严重的组织。本研究中获得的新知识可能对于考虑通过饮食中的营养成分直接调节基因表达具有潜在价值。