# Fasting-Induced Changes in Serum Kynurenines Do Not Always Reflect Their Urinary Excretion

**Authors:** Zuzanna Margas, Andżelika Borkowska, Konrad Kowalski, Ulana Juhas, Joanna Reczkowicz, Jakub Kortas, Anna Pilis, Inga Cytrych, Ewa Ziemann, Jędrzej Antosiewicz

PMC · DOI: 10.3390/nu18040689 · Nutrients · 2026-02-20

## TL;DR

Fasting increases most serum kynurenines but does not always increase their urinary excretion, suggesting complex regulation of these metabolites.

## Contribution

This study is the first to compare fasting effects on serum and urinary kynurenines, revealing discrepancies in excretion patterns.

## Key findings

- Fasting increased serum 3-HK, AA, PA, KYNA, and XANA but decreased KYN and QA.
- Urinary excretion increased for KYN, 3-HK, XANA, and QA but not for AA and PA.
- Serum KYN and QA decreases may result from enhanced urinary elimination.

## Abstract

Background: The effects of fasting on serum kynurenines (KYNs) have been reported; however, no data are available on whether fasting also modifies their urinary excretion. Kidney organic anion transporters are involved in KYNs excretion, suggesting that changes in serum levels may result from altered urinary elimination. Considering the important role of KYNs in regulating various physiological processes, it is crucial to understand the factors that determine their blood concentrations. The present study aimed to determine the effect of an 8-day fasting period on the concentrations of KYNs in both serum and urine. Methods: Thirteen participants underwent an 8-day fast. The exercise test was performed at baseline after an overnight fast and after 8 days of fasting. Results: Fasting increased the serum concentrations of 3-hydroxykynurenine (3-HK), anthranilic acid (AA), picolinic acid (PA), kynurenic acid (KYNA), and xanthurenic acid (XANA). Conversely, serum kynurenine (KYN) and quinolinic acid (QA) decreased, while 3-hydroxyanthranilic acid (3-HAA) remained unchanged. In urine, KYN, 3-HK, XANA and QA increased after fasting, whereas AA and PA did not change. Conclusions: In conclusion, these findings indicate that fasting generally increases serum kynurenines (KYNs), which are associated with enhanced urinary excretion, suggesting that fasting may stimulate their synthesis. In the case of anthranilic acid (AA) and picolinic acid (PA), their increase in serum does not influence their urinary excretion. Conversely, a decrease in serum KYN and quinolinic acid (QA) may result from enhanced urinary excretion.

## Linked entities

- **Chemicals:** 3-hydroxykynurenine (PubChem CID 89), anthranilic acid (PubChem CID 227), picolinic acid (PubChem CID 1018), kynurenic acid (PubChem CID 3845), xanthurenic acid (PubChem CID 5699), kynurenine (PubChem CID 846), quinolinic acid (PubChem CID 1066), 3-hydroxyanthranilic acid (PubChem CID 86)

## Full-text entities

- **Genes:** IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620] {aka IDO, IDO-1, INDO}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, TSTD1 (thiosulfate sulfurtransferase like domain containing 1) [NCBI Gene 100131187] {aka KAT}, KYNU (kynureninase) [NCBI Gene 8942] {aka KYNUU, VCRL2}, KMO (kynurenine 3-monooxygenase) [NCBI Gene 8564] {aka dJ317G22.1}, SLC22A6 (solute carrier family 22 member 6) [NCBI Gene 9356] {aka HOAT1, OAT1, PAHT, ROAT1}, OAT (ornithine aminotransferase) [NCBI Gene 4942] {aka GACR, HOGA, OATASE, OKT}, SLC22A8 (solute carrier family 22 member 8) [NCBI Gene 9376] {aka OAT3}
- **Diseases:** chronic diseases (MESH:D002908), dementia (MESH:D003704), depression (MESH:D003866), osteoporosis (MESH:D010024), neurotoxic (MESH:D020258), diabetes (MESH:D003920), COVID-19 (MESH:D000086382), pulmonary arterial hypertension (MESH:D000081029), inflammation (MESH:D007249), neurodegeneration (MESH:D019636), injury to (MESH:D014947)
- **Chemicals:** 3-HK (MESH:C005045), creatinine (MESH:D003404), QA (MESH:D017378), AA (MESH:C031385), dopamine (MESH:D004298), PA (MESH:C030614), HCl (MESH:D006851), KYNs (MESH:D007737), alcohol (MESH:D000438), Trp (MESH:D014364), H2O (MESH:D014867), XANA (MESH:C028330), acetonitrile (MESH:C032159), 3-HAA (MESH:D015095), KYNA (MESH:D007736), N2 (MESH:D009584), probenecid (MESH:D011339), formic acid (MESH:C030544), 1-butanol (MESH:D020001), oxygen (MESH:D010100), 2H3-3HAA (-)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943222/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943222/full.md

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Source: https://tomesphere.com/paper/PMC12943222