Quantification of Plasma Kynurenine Metabolites Following One Bout of Sprint Interval Exercise

Author:

Trepci Ada12,Imbeault Sophie1,Wyckelsma Victoria L1ORCID,Westerblad Håkan12,Hermansson Sigurd3,Andersson Daniel C14,Piehl Fredrik56,Venckunas Tomas2,Brazaitis Marius2,Kamandulis Sigitas2,Brundin Lena178,Erhardt Sophie1ORCID,Schwieler Lilly1

Affiliation:

1. Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden

2. Institute of Sport Science and Innovations, Lithuanian Sports University, Kaunas, Lithuania

3. Waters Sverige AB, Stockholm, Sweden

4. Cardiology Unit, Heart, Vascular and Neurology Theme; Karolinska University Hospital, Stockholm, Sweden

5. Neuroimmunology Unit, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden

6. Division of Neurology, Karolinska University Hospital, Stockholm, Sweden

7. Center for Neurodegenerative Science, Van Andel Research Institute, Grand Rapids, MI, USA

8. Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Psychiatry, Lund, Sweden

Abstract

The kynurenine pathway of tryptophan degradation produces several neuroactive metabolites suggested to be involved in a wide variety of diseases and disorders, however, technical challenges in reliably detecting these metabolites hampers cross-comparisons. The main objective of this study was to develop an accurate, robust and precise bioanalytical method for simultaneous quantification of ten plasma kynurenine metabolites. As a secondary aim, we applied this method on blood samples taken from healthy subjects conducting 1 session of sprint interval exercise (SIE). It is well accepted that physical exercise is associated with health benefits and reduces risks of psychiatric illness, diabetes, cancer and cardiovascular disease, but also influences the peripheral and central concentrations of kynurenines. In line with this, we found that in healthy old adults ( n = 10; mean age 64 years), levels of kynurenine increased 1 hour ( P = .03) after SIE, while kynurenic acid (KYNA) concentrations were elevated after 24 hours ( P = .02). In contrast, no significant changes after exercise were seen in young adults ( n = 10; mean age 24 years). In conclusion, the described method performs well in reliably detecting all the analyzed metabolites in plasma samples. Furthermore, we also detected an age-dependent effect on the degree by which a single intense training session affects kynurenine metabolite levels.

Publisher

SAGE Publications

Subject

Molecular Biology,Biochemistry

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