Cardiovascular Nutrition Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging; Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA, USA.
USDA, ARS, Beltsville Human Nutrition Research Center, Diet Genomics and Immunology Laboratory, Beltsville, MD, USA.
J Nutr Biochem. 2021 Apr;90:108577. doi: 10.1016/j.jnutbio.2020.108577. Epub 2020 Dec 31.
Diet quality and statin therapy are established modulators of coronary artery disease (CAD) progression, but their effect on the gastrointestinal tract and subsequent sequelae that could affect CAD progression are relatively unexplored. To address this gap, Ossabaw pigs (N = 32) were randomly assigned to receive isocaloric amounts of a Western-type diet (WD; high in saturated fat, refined carbohydrate, and cholesterol, and low in fiber) or a heart healthy-type diet (HHD; high in unsaturated fat, whole grains, fruits and vegetables, supplemented with fish oil, and low in cholesterol), with or without atorvastatin, for 6 months. At the end of the study, RNA sequencing with 100 base pair single end reads on NextSeq 500 platform was conducted in isolated pig jejunal mucosa. A two-factor edgeR analysis revealed that the dietary patterns resulted in three differentially expressed genes related to lipid metabolism (SCD, FADS1, and SQLE). The expression of these genes was associated with cardiometabolic risk factors and atherosclerotic lesion severity. Subsequent gene enrichment analysis indicated the WD, compared to the HHD, resulted in higher interferon signaling and inflammation, with some of these genes being significantly associated with serum TNF-α and/or hsCRP concentrations, but not atherosclerotic lesion severity. No significant effect of atorvastatin therapy on gene expression, nor its interaction with dietary patterns, was identified. In conclusion, Western and heart healthy-type dietary patterns differentially affect the expression of genes associated with lipid metabolism, interferon signaling, and inflammation in the jejunum of Ossabaw pigs.
饮食质量和他汀类药物治疗是冠心病(CAD)进展的既定调节剂,但它们对胃肠道的影响以及随后可能影响 CAD 进展的后果相对较少被探索。为了解决这一差距,奥萨鲍(Ossabaw)猪(N=32)被随机分配接受等热量的西式饮食(WD;富含饱和脂肪、精制碳水化合物和胆固醇,纤维含量低)或心脏健康型饮食(HHD;富含不饱和脂肪、全谷物、水果和蔬菜,补充鱼油,胆固醇含量低),并同时或不同时给予阿托伐他汀治疗,为期 6 个月。在研究结束时,使用 NextSeq 500 平台进行 100 碱基对单端读取的 RNA 测序,对分离的猪空肠黏膜进行测序。双因素 edgeR 分析显示,饮食模式导致了 3 个与脂质代谢相关的差异表达基因(SCD、FADS1 和 SQLE)。这些基因的表达与心血管代谢风险因素和动脉粥样硬化病变严重程度相关。随后的基因富集分析表明,与 HHD 相比,WD 导致更高的干扰素信号和炎症,其中一些基因与血清 TNF-α 和/或 hsCRP 浓度显著相关,但与动脉粥样硬化病变严重程度无关。阿托伐他汀治疗对基因表达没有显著影响,也没有发现其与饮食模式的相互作用。总之,西方和心脏健康型饮食模式在奥萨鲍猪空肠中对与脂质代谢、干扰素信号和炎症相关的基因表达产生了不同的影响。