Department of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa Carver College of Medicine, Iowa City, IA 52242.
Department of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa Carver College of Medicine, Iowa City, IA 52242
J Lipid Res. 2020 Aug;61(8):1161-1167. doi: 10.1194/jlr.R120000922. Epub 2020 Jun 25.
The risk for metabolic disease, including metabolic syndrome, insulin resistance, and diabetes, increases with age. Altered plasma TG metabolism and changes in fatty acid partitioning are also major contributors to metabolic disease. Plasma TG metabolism itself is altered by age in humans and rodents. As discussed in this review, the age-induced changes in human TG metabolism include increased plasma TG levels, reduced postprandial plasma TG clearance rates, reduced postheparin LPL activity, decreased adipose tissue lipolysis, and elevated ectopic fat deposition, all of which could potentially contribute to age-associated metabolic diseases. Similar observations have been made in aged rats. We highlight the limitations of currently available data and propose that mechanistic studies are needed to understand the extent to which age-induced alterations in TG metabolism contribute to metabolic disease. Such mechanistic insights could aid in therapeutic strategies for preventing or managing metabolic disease in older individuals.
随着年龄的增长,代谢性疾病(包括代谢综合征、胰岛素抵抗和糖尿病)的风险也会增加。血浆甘油三酯(TG)代谢的改变和脂肪酸分布的变化也是代谢性疾病的主要原因。人类和啮齿动物的血浆 TG 代谢本身会随着年龄的增长而发生变化。正如本综述中所讨论的,人类 TG 代谢的年龄诱导变化包括血浆 TG 水平升高、餐后血浆 TG 清除率降低、肝素后脂蛋白脂肪酶(LPL)活性降低、脂肪组织脂解减少和异位脂肪沉积增加,所有这些都可能导致与年龄相关的代谢性疾病。在老年大鼠中也观察到了类似的现象。我们强调了现有数据的局限性,并提出需要进行机制研究,以了解 TG 代谢的年龄诱导改变在多大程度上导致代谢性疾病。这种机制上的见解可以帮助制定预防或治疗老年人代谢性疾病的治疗策略。