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Plasma acylcarnitine levels increase with healthy aging

机译:血浆酰基氨基氨基水平随着健康老化的增加

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摘要

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 ( ) 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.
机译:酰基羧碱将脂肪酸转化为线粒体,对β-氧化和能量代谢至关重要。降低的线粒体活性导致增加的血浆酰基酰基氨基碱,并且增加的酰基碱激活促炎信号和与年龄相关疾病的助剂。然而,与健康衰老相关的酰基羧酸甘油的变化并不具备很好的表征。在本研究中,我们研究了来自预测性医学研究队列()的163名健康,非患病的年龄(范围:20-90)的血浆酰基氨基甲酰胺的关联,并对性别特异性差异进行了测试。结果表明,长链和非常长的酰基氨基碱随着年龄的增长而增加,而许多奇数链酰基氨基碱随着年龄的增长而降低。几种酰基甘油碱观察到性别特异性差异,例如,均沙染生碱随着男性年龄而变化,羟基甲酰氨基在雌性中变化。具有所有未明确的代谢特征的年龄相关酰基甘油碱的代谢物 - 宽协会研究(MWA)在性别之间表现出很少的重叠。这些结果表明,在选择健康标准的个体中,血浆浓度随年龄和性别而变化。这些变异是否反映了随老化的线粒体功能障碍,针对慢性环境暴露的线粒体重编程,早期预疾病变化或对健康老化的适应性反应,尚不清楚。结果突出了未设定的代谢组科研究的潜在效用,以阐明衰老和年龄相关疾病的性别特异性机制。

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