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血浆酰基肉碱水平随着健康衰老而增加。

Plasma acylcarnitine levels increase with healthy aging.

机构信息

Division of Pulmonary, Allergy and Critical Care Medicine, Atlanta, GA 30322, USA.

Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Aging (Albany NY). 2020 Jun 16;12(13):13555-13570. doi: 10.18632/aging.103462.

DOI:10.18632/aging.103462
PMID:32554854
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7377890/
Abstract

Acylcarnitines transport fatty acids into mitochondria and are essential for β-oxidation and energy metabolism. Decreased mitochondrial activity results in increased plasma acylcarnitines, and increased acylcarnitines activate proinflammatory signaling and associate with age-related disease. Changes in acylcarnitines associated with healthy aging, however, are not well characterized. In the present study, we examined the associations of plasma acylcarnitines with age (range: 20-90) in 163 healthy, non-diseased individuals from the predictive medicine research cohort (NCT00336570) and tested for gender-specific differences. The results show that long-chain and very long-chain acylcarnitines increased with age, while many odd-chain acylcarnitines decreased with age. Gender-specific differences were observed for several acylcarnitines, e.g., eicosadienoylcarnitine varied with age in males, and hydroxystearoylcarnitine varied in females. Metabolome-wide association study (MWAS) of age-associated acylcarnitines with all untargeted metabolic features showed little overlap between genders. These results show that plasma concentrations of acylcarnitines vary with age and gender in individuals selected for criteria of health. Whether these variations reflect mitochondrial dysfunction with aging, mitochondrial reprogramming in response to chronic environmental exposures, early pre-disease change, or an adaptive response to healthy aging, is unclear. The results highlight a potential utility for untargeted metabolomics research to elucidate gender-specific mechanisms of aging and age-related disease.

摘要

酰基辅酶 A 转运脂肪酸进入线粒体,对于β-氧化和能量代谢是必不可少的。线粒体活性的降低导致血浆酰基辅酶 A 增加,而增加的酰基辅酶 A 会激活促炎信号,并与年龄相关的疾病相关联。然而,与健康衰老相关的酰基辅酶 A 变化尚未得到很好的描述。在本研究中,我们研究了与年龄(范围:20-90 岁)相关的血浆酰基辅酶 A 在 163 名来自预测医学研究队列(NCT00336570)的健康、无疾病个体中的相关性,并测试了性别特异性差异。结果表明,长链和超长链酰基辅酶 A 随着年龄的增长而增加,而许多奇数链酰基辅酶 A 随着年龄的增长而减少。几种酰基辅酶 A 存在性别特异性差异,例如,二十碳二烯酰基辅酶 A 在男性中随年龄而变化,而羟十八碳酰基辅酶 A 在女性中随年龄而变化。对与所有非靶向代谢特征相关的年龄相关酰基辅酶 A 进行代谢组学全基因组关联研究(MWAS)显示,性别之间几乎没有重叠。这些结果表明,在选择健康标准的个体中,血浆酰基辅酶 A 的浓度随年龄和性别而变化。这些变化是否反映了衰老过程中线粒体功能障碍、慢性环境暴露的线粒体重编程、早期疾病前变化或健康衰老的适应性反应,目前尚不清楚。这些结果突出表明,非靶向代谢组学研究具有阐明性别特异性衰老和与年龄相关疾病机制的潜力。

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