Decreased kynurenine in cerebrospinal fluid and potential role in neuromyelitis optica spectrum disorder. Issue 2 (17th February 2023)

• Record Type: Journal Article
• Authors: Peng, Fuhua; She, Hongda; Wang, Yuge; Xu, Li; Shan, Yilong; Chang, Yanyu; Zhong, Xiaonan; Li, Rui; Qiu, Wei; Shu, Yaqing; Tan, Sha
• Is Part Of: Journal of neurochemistry. Volume 165:Issue 2(2023)
• Page Start: 259
• Page End: 267
• Publication Date: 2023-02-17
• Subjects: AQP4 -- Cerebrospinal fluid -- Kynurenine -- NMOSD -- NMOSD‐IgG -- Relapse -- Tryptophan metabolism; Neurochemistry -- Periodicals; 616.8042
• DOI: 10.1111/jnc.15772
• Languages: English
• ISSNs: 0022-3042

Abstract

Abstract: Tryptophan (Trp) metabolism has been implicated in neuroinflammatory and neurodegenerative disorders, but its relationship with neuromyelitis optica spectrum disorder (NMOSD) is unclear. In this pilot study, cerebrospinal fluid (CSF) was prospectively collected from 26 NMOSD patients in relapse and 16 controls with noninflammatory diseases and 6 neurometabolites in the tryptophan metabolic pathway, including 5‐hydroxytryptamine (5‐HT), kynurenine (KYN), melatonin (MLT), 5‐hydroxyindoleacetic acid (5HIAA), 3‐hydroxy‐o‐aminobenzoic acid (3‐HAA), and kynurenic acid (KYA), were measured by ultrahigh‐performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS). The association of Trp metabolites with NMOSD and its clinical parameters was evaluated. The role of KYN, which is a Trp metabolite involved in the binding of NMOSD‐IgG antibody to aquaporin 4 (AQP4), was also evaluated in vitro. CSF KYN was significantly decreased in patients with relapsing NMOSD compared to controls, and CSF KYN was associated with CSF white blood cells in NMOSD. In vitro experiments showed that NMOSD‐IgG specifically recognized KYN, which reversed the NMOSD‐IgG‐induced downregulation of AQP4 expression. Our results show that abnormal Trp metabolism occurs in NMOSD and that KYN might be a potential target for the treatment of AQP4‐IgG‐positive NMOSD patients. Abstract : We found CSF KYN was significantly decreased in patients with relapsing NMOSD compared to controls. In vitro experiments showed that NMOSD‐IgG specifically recognized KYN, which reversed the NMOSD‐IgG‐induced downregulation of AQP4 expression. Our results show that abnormal Trp metabolism occurs in NMOSD and that KYN might be a potential target for the treatment of AQP4‐IgG‐positive NMOSD patients.