Abstract

Multiple sclerosis is an autoimmune, demyelinating, and neurodegenerative disease of the central nervous system. In recent years, it has been proven that the kynurenine system plays a significant role in the development of several nervous system disorders, including multiple sclerosis. Kynurenine pathway metabolites have both neurotoxic and neuroprotective effects. Moreover, the enzymes of the kynurenine pathway play an important role in immunomodulation processes, among others, as well as interacting with neuronal energy balance and various redox reactions. Dysregulation of many of the enzymatic steps in kynurenine pathway and upregulated levels of these metabolites locally in the central nervous system, contribute to the progression of multiple sclerosis pathology. This process can initiate a pathogenic cascade, including microglia activation, glutamate excitotoxicity, chronic oxidative stress or accumulated mitochondrial damage in the axons, that finally disrupt the homeostasis of neurons, leads to destabilization of neuronal cell cytoskeleton, contributes to neuro-axonal damage and neurodegeneration. Neurofilaments are good biomarkers of the neuro-axonal damage and their level reliably indicates the severity of multiple sclerosis and the treatment response. There is increasing evidence that connections exist between the molecules generated in the kynurenine metabolic pathway and the change in neurofilament concentrations. Thus the alterations in the kynurenine pathway may be an important biomarker of the course of multiple sclerosis. In our present review, we report the possible relationship and connection between neurofilaments and the kynurenine system in multiple sclerosis based on the available evidences.

Highlights

  • Multiple sclerosis (MS) is an immune-mediated, chronic inflammatory and demyelinating disease of the central nervous system (CNS), which affects both gray and white matter (Bo et al, 2006)

  • We focus on the cells which produce these metabolites and the mechanism of action how they cause the neuro-axonal damage leading to neurodegeneration

  • relapsing-remitting MS (RRMS) patients demonstrated elevated quinolinic acid (QUIN) levels and higher QUIN/kynurenine ratio during relapse and lower TRP and kynurenic acid (KYNA) levels have been measured in secondary progressive MS (SPMS) patients (Aeinehband et al, 2016). These results suggest that the kynurenine pathway (KP) is induced during the active phase of MS and leads to increased KYNA production, while during the progressive phase of the disease QUIN levels increase and KYNA levels decrease indicating a change in the KP profile during progression (Rejdak et al, 2002, 2007; Hartai et al, 2005)

Read more

Summary

Introduction

Multiple sclerosis (MS) is an immune-mediated, chronic inflammatory and demyelinating disease of the central nervous system (CNS), which affects both gray and white matter (Bo et al, 2006). This section discusses the metabolites with a potential role in the development of MS, including the free radical forming 3-HK, the pro-oxidant, glutamate excitotoxicity inducing, neurotoxic QUIN, and the potentially neuroprotective KYNA.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.