International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(3), P. 976 - 976
Published: Jan. 24, 2025
The cuprizone (CPZ) model of multiple sclerosis (MS) is excellent for studying the molecular differences behind damage caused by poisoning. Metabolic in kynurenine pathway (KP) tryptophan (TRP) degradation are observed both MS and a CPZ mouse model. Our goal was to analyze kynurenine, serotonin, indole pathways TRP on periphery, neurodegenerative processes inflammation. In our study, mice were fed with 0.2% toxin 5 weeks. We examined metabolites three breakdown urine, plasma, relevant visceral organs bioanalytical measurements. analyses, we found significant increase plasma TRP, 5-hydroxytryptophan (5-HTP), indole-3-acetic acid (IAA) levels, while decrease concentrations 3-hydroxy-L-kynurenine (3-HK), xanthurenic (XA), kynurenic (KYNA), quinaldic toxin-treated group found. A marked levels 3-HK, XA, KYNA, acid, indole-3-lactic also end Furthermore, noticed urinary XA metabolites, an serotonin 5-hydroxyindoleacetic noticed. treatment resulted elevated tryptamine indoxyl sulfate reduced IAA concentration. Moreover, para-cresyl concentration increased treated group. present showed main metabolic confirmed relationship correlation between content tissues organs. emphasized suppression KP activity particular regard involvement microbiome pathway. Consequently, this first study detail distribution periphery.
Language: Английский