The Tryptophan-Kynurenine Metabolic System Is Suppressed in Cuprizone-Induced Model of Demyelination Simulating Progressive Multiple Sclerosis

Progressive multiple sclerosis (MS) is a chronic disease with a unique pattern, which is histologically classified into the subpial type 3 lesions in the autopsy. The lesion is also homologous to that of cuprizone (CPZ) toxin-induced animal models of demyelination. Aberration of the tryptophan (TRP)...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Polyák Helga
Galla Zsolt
Nánási Nikolett
Cseh Edina Katalin
Rajda Cecília
Veres Gábor
Spekker Eleonóra
Szabó Ágnes
Klivényi Péter
Tanaka Masaru
Vécsei László
Dokumentumtípus: Cikk
Megjelent: 2023
Sorozat:BIOMEDICINES 11 No. 3
Tárgyszavak:
doi:10.3390/biomedicines11030945

mtmt:33709302
Online Access:http://publicatio.bibl.u-szeged.hu/26787
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245 1 4 |a The Tryptophan-Kynurenine Metabolic System Is Suppressed in Cuprizone-Induced Model of Demyelination Simulating Progressive Multiple Sclerosis  |h [elektronikus dokumentum] /  |c  Polyák Helga 
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490 0 |a BIOMEDICINES  |v 11 No. 3 
520 3 |a Progressive multiple sclerosis (MS) is a chronic disease with a unique pattern, which is histologically classified into the subpial type 3 lesions in the autopsy. The lesion is also homologous to that of cuprizone (CPZ) toxin-induced animal models of demyelination. Aberration of the tryptophan (TRP)-kynurenine (KYN) metabolic system has been observed in patients with MS; nevertheless, the KYN metabolite profile of progressive MS remains inconclusive. In this study, C57Bl/6J male mice were treated with 0.2% CPZ toxin for 5 weeks and then underwent 4 weeks of recovery. We measured the levels of serotonin, TRP, and KYN metabolites in the plasma and the brain samples of mice at weeks 1, 3, and 5 of demyelination, and at weeks 7 and 9 of remyelination periods by ultra-high-performance liquid chromatography with tandem mass spectrometry (UHPLC-MS/MS) after body weight measurement and immunohistochemical analysis to confirm the development of demyelination. The UHPLC-MS/MS measurements demonstrated a significant reduction of kynurenic acid, 3-hydoxykynurenine (3-HK), and xanthurenic acid in the plasma and a significant reduction of 3-HK, and anthranilic acid in the brain samples at week 5. Here, we show the profile of KYN metabolites in the CPZ-induced mouse model of demyelination. Thus, the KYN metabolite profile potentially serves as a biomarker of progressive MS and thus opens a new path toward planning personalized treatment, which is frequently obscured with immunologic components in MS deterioration. 
650 4 |a Klinikai orvostan 
700 0 1 |a Galla Zsolt  |e aut 
700 0 1 |a Nánási Nikolett  |e aut 
700 0 1 |a Cseh Edina Katalin  |e aut 
700 0 1 |a Rajda Cecília  |e aut 
700 0 1 |a Veres Gábor  |e aut 
700 0 1 |a Spekker Eleonóra  |e aut 
700 0 1 |a Szabó Ágnes  |e aut 
700 0 1 |a Klivényi Péter  |e aut 
700 0 1 |a Tanaka Masaru  |e aut 
700 0 1 |a Vécsei László  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/26787/1/PolyakH._thetryptophan-kynureninemetabolicsystem....pdf  |z Dokumentum-elérés