Kynurenine pathway metabolites selectively associate with impaired associative memory function in depression

Margherita Chirico, James Custer, Ifeoluwa Shoyombo, Crystal Cooper Cortes, Sheila Meldrum, Robert Dantzer, Madhukar H. Trivedi, Paul Rathouz, Marisa S. Toups

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


Activation of the kynurenine pathway (KP), an important downstream effect of inflammation, is a driver of depression and neurodegeneration. Damage from the end product of KP activation, quinolinic acid, may be responsible specifically for impairment in hippocampally mediated memory function, among its effects. We hypothesized that associative memory – the ability to recall relationships between items – would be sensitive to KP activation because it is heavily dependent on the hippocampus. We tested a sample of N ​= ​80 adults with unmedicated depression using a face-name task which assesses the ability to recognize, as well as to recall correct pairings, of faces and names. Plasma samples were analyzed for KP metabolites – tryptophan (TRP), kynurenine (KYN), quinolinic acid (QUIN) and kynurenic acid (KYNA). Using linear models we examined whether the KYN/TRP and QUIN/KYNA ratios predicted performance of recognition memory and associative memory, accounting for item type and the number of learning exposures to items (1 vs. 3). We found that for rearranged items viewed three times, associative memory performance was inversely related to the QUIN/KYNA ratio (p ​= ​0.01, p ​= ​0.001 adjusted for age, gender and race/ethnicity). Recognition memory was not associated with KP activation. The results support our hypothesis that KP activation most sensitively impacts hippocampally mediated memory function.

Original languageEnglish (US)
Article number100126
JournalBrain, Behavior, and Immunity - Health
StatePublished - Oct 2020


  • Cognition
  • Depression
  • Kynurenine
  • Memory

ASJC Scopus subject areas

  • Nephrology


Dive into the research topics of 'Kynurenine pathway metabolites selectively associate with impaired associative memory function in depression'. Together they form a unique fingerprint.

Cite this