喹啉酸
炎症
犬尿氨酸
犬尿氨酸途径
谷氨酸受体
神经科学
握力
神经退行性变
CX3CR1型
医学
内科学
内分泌学
生物
色氨酸
生理学
生物化学
受体
氨基酸
疾病
趋化因子受体
趋化因子
作者
Reyhan Westbrook,Tae Hwan Chung,Jacqueline Lovett,Christopher W. Ward,Humberto C. Joca,Huanle Yang,Mohammed Khadeer,Jing Tian,Qian‐Li Xue,Anne Le,Luigi Ferrucci,Ruin Moaddel,Rafael de Cabo,Ahmet Höke,Jeremy Walston,Peter M. Abadir
出处
期刊:JCI insight
[American Society for Clinical Investigation]
日期:2020-08-20
卷期号:5 (16)
被引量:63
标识
DOI:10.1172/jci.insight.136091
摘要
Chronic inflammation is associated with physical frailty and functional decline in older adults; however, the molecular mechanisms of this linkage are not understood. A mouse model of chronic inflammation showed reduced motor function and partial denervation at the neuromuscular junction. Metabolomic profiling of these mice and further validation in frail human subjects showed significant dysregulation in the tryptophan degradation pathway, including decreased tryptophan and serotonin, and increased levels of some neurotoxic kynurenines. In humans, kynurenine strongly correlated with age, frailty status, TNF-αR1 and IL-6, weaker grip strength, and slower walking speed. To study the effects of elevated neurotoxic kynurenines on motor neuronal cell viability and axonal degeneration, we used motor neuronal cells treated with 3-hydroxykynurenine and quinolinic acid and observed neurite degeneration in a dose-dependent manner and potentiation of toxicity between 3-hydroxykynurenine and quinolinic acid. These results suggest that kynurenines mediate neuromuscular dysfunction associated with chronic inflammation and aging.
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