4.7 Article

Kynurenines link chronic inflammation to functional decline and physical frailty

期刊

JCI INSIGHT
卷 5, 期 16, 页码 -

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/jci.insight.136091

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资金

  1. Johns Hopkins Older Americans Independence Center National Institute on Aging [P30 AG021334]
  2. NIH [R01AG046441, K23 AG035005]
  3. Bright Focus Foundation Research Award
  4. Nathan W. and Margaret T. Shock Aging Research Foundation
  5. Nathan Shock Scholar in Aging
  6. American Federation for Aging Research
  7. Secunda Family Foundation [K08 AG058483, R01 AR071618, P30-AG028747]
  8. Baltimore Veterans Affairs Medical Center Geriatric Education Clinical Center (GRECC)
  9. Miriam and Sheldon G. Adelson Medical Foundation
  10. National Institute on Aging

向作者/读者索取更多资源

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-alpha R1 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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