National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan.
PLoS One. 2012;7(5):e37581. doi: 10.1371/journal.pone.0037581. Epub 2012 May 25.
Hyperlipidemia animal models have been established, but complete gene expression profiles of the transition from normal lipid levels have not been obtained. Miniature pigs are useful model animals for gene expression studies on dietary-induced hyperlipidemia because they have a similar anatomy and digestive physiology to humans, and blood samples can be obtained from them repeatedly.
Two typical dietary treatments were used for dietary-induced hyperlipidemia models, by using specific pathogen-free (SPF) Clawn miniature pigs. One was a high-fat and high-cholesterol diet (HFCD) and the other was a high-fat, high-cholesterol, and high-sucrose diet (HFCSD). Microarray analyses were conducted from whole blood samples during the dietary period and from white blood cells at the end of the dietary period to evaluate the transition of expression profiles of the two dietary models.
Variations in whole blood gene expression intensity within the HFCD or the HFCSD group were in the same range as the controls provide with normal diet at all periods. This indicates uniformity of dietary-induced hyperlipidemia for our dietary protocols. Gene ontology- (GO) based functional analyses revealed that characteristics of the common changes between HFCD and HFCSD were involved in inflammatory responses and reproduction. The correlation coefficient between whole blood and white blood cell expression profiles at 27 weeks with the HFCSD diet was significantly lower than that of the control and HFCD diet groups. This may be due to the effects of RNA originating from the tissues and/or organs.
No statistically significant differences in fasting plasma lipids and glucose levels between the HFCD and HFCSD groups were observed. However, blood RNA analyses revealed different characteristics corresponding to the dietary protocols. In this study, whole blood RNA analyses proved to be a useful tool to evaluate transitions in dietary-induced hyperlipidemia gene expression profiles in miniature pigs.
已经建立了高脂血症动物模型,但尚未获得正常血脂水平转变的完整基因表达谱。小型猪是研究饮食诱导高脂血症基因表达的有用模型动物,因为它们的解剖结构和消化生理学与人类相似,并且可以从它们身上反复采集血样。
使用特定病原体(SPF)克劳恩小型猪,使用两种典型的饮食处理方法建立饮食诱导的高脂血症模型。一种是高脂肪高胆固醇饮食(HFCD),另一种是高脂肪、高胆固醇和高蔗糖饮食(HFCSD)。在饮食期间,从全血样本和饮食结束时从白细胞中进行微阵列分析,以评估两种饮食模型的表达谱转变。
在 HFCD 或 HFCSD 组中,全血基因表达强度的变化在各个时期与提供正常饮食的对照组相同。这表明我们的饮食方案诱导的高脂血症具有一致性。基于基因本体论(GO)的功能分析表明,HFCD 和 HFCSD 之间共同变化的特征涉及炎症反应和生殖。用 HFCSD 饮食喂养 27 周时,全血和白细胞表达谱之间的相关系数明显低于对照组和 HFCD 饮食组。这可能是由于来自组织和/或器官的 RNA 的影响。
HFCD 和 HFCSD 组之间的空腹血浆脂质和葡萄糖水平没有统计学上的显著差异。然而,血液 RNA 分析显示出与饮食方案相对应的不同特征。在这项研究中,全血 RNA 分析被证明是评估小型猪饮食诱导高脂血症基因表达谱转变的有用工具。