Department of Veterinary and Biomedical Sciences and Center for Excellence in Nutrigenomics, Penn State University, University Park, Pennsylvania, USA.
Prog Mol Biol Transl Sci. 2012;108:75-112. doi: 10.1016/B978-0-12-398397-8.00004-6.
Diets rich in ω3 polyunsaturated fatty acids (ω3-PUFAs) such as alpha-linolenic acid, eicosapentaenoic acid, and docosahexaenoic acid are associated with decreased incidence and severity of several chronic diseases including cardiovascular disease (CVD) and cancer. At least some of the beneficial effects of these dietary fatty acids are via metabolites such as prostaglandins, leukotrienes, thromboxanes, and resolvins. The effects of ω3-PUFAs are in contrast to those of fatty acids with virtually identical structures, such as the ω6-PUFAs linoleic acid and arachidonic acid, and their corresponding metabolites. The purpose of this chapter is to discuss both the nutrigenomics (nutrient-gene interactions) and nutrigenetics (genetic variation in nutrition) of dietary fatty acids with a focus on the ω3-PUFAs (Gebauer et al., 2007(1)). Important in the biological response for these fatty acids or their metabolites are cognate receptors that are able to regulate gene expression and coordinately affect metabolic or signaling pathways associated with CVD and cancer. Four nuclear receptor (NR) subfamilies will be emphasized as receptors that respond to dietary and endogenous ligands: (1) peroxisome proliferator-activated receptors, (2) retinoid X receptors, (3) liver X receptors, and (4) farnesoid X receptor. In addition to the different responses elicited by varying structures of fatty acids, responses may vary because of genetic variation in enzymes that metabolize ω3- and ω6 fatty acids or that respond to them. In particular, polymorphisms in the fatty acid desaturases and the aforementioned NRs contribute to the complexity of nutritional effects seen with ω3-PUFAs. Following a brief introduction to the health benefits of ω3-PUFAs, the regulation of gene expression by these dietary fatty acids via NRs will be characterized. Subsequently, the effects of single-nucleotide polymorphisms (SNPs) in key enzymes involved in the metabolism and response to ω3-PUFAs will be described. An outline of the events to be explored is shown in Fig. 1. Understanding the nutrigenomics and nutrigenetics of dietary fatty acids is key to understanding the etiology, as well as prevention, of critically important human diseases including CVD and cancer.
富含 ω3 多不饱和脂肪酸(ω3-PUFAs)的饮食,如α-亚麻酸、二十碳五烯酸和二十二碳六烯酸,与多种慢性疾病的发病率和严重程度降低有关,包括心血管疾病(CVD)和癌症。这些膳食脂肪酸的一些有益作用至少部分是通过代谢产物如前列腺素、白三烯、血栓素和解析素实现的。ω3-PUFAs 的作用与具有几乎相同结构的脂肪酸(如 ω6-PUFAs 亚油酸和花生四烯酸)及其相应的代谢产物相反。本章的目的是讨论膳食脂肪酸的营养基因组学(营养素-基因相互作用)和营养遗传学(营养的遗传变异),重点是 ω3-PUFAs(Gebauer 等人,2007(1))。对于这些脂肪酸或其代谢产物,重要的是能够调节基因表达并协调影响与 CVD 和癌症相关的代谢或信号通路的同源受体。将强调四个核受体(NR)亚家族作为对膳食和内源性配体有反应的受体:(1)过氧化物酶体增殖物激活受体,(2)视黄酸 X 受体,(3)肝 X 受体,和(4)法尼醇 X 受体。除了不同结构的脂肪酸引起的不同反应外,由于代谢 ω3-和 ω6 脂肪酸或对其作出反应的酶的遗传变异,反应也可能有所不同。特别是,脂肪酸去饱和酶和上述 NR 中的多态性导致了 ω3-PUFAs 所表现出的复杂的营养效应。在简要介绍 ω3-PUFAs 的健康益处后,将描述这些膳食脂肪酸通过 NR 对基因表达的调节。随后,将描述参与 ω3-PUFAs 代谢和反应的关键酶中的单核苷酸多态性(SNP)的影响。如图 1 所示,概述了将要探索的事件。了解膳食脂肪酸的营养基因组学和营养遗传学是理解包括心血管疾病(CVD)和癌症在内的重要人类疾病的病因以及预防的关键。