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The Role of Oxidative Stress in TB Meningitis and Therapeutic Options
John Dawi1, Aishvaryaa Shree Mohan1, Yura Misakyan1
1College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, CA 91766, USA.
Abstract:
Meningitis is an inflammatory condition affecting the meninges surrounding the brain and spinal cord. Meningitis can be triggered by various factors, including infectious agents like viruses and bacteria and non-infectious contributors such as cancer or head injuries. The impact of meningitis on the central nervous system involves disruptions in the blood-brain barrier, cellular infiltrations, and structural alterations. The clinical features that differentiate between tuberculous meningitis (TBM) and non-tuberculous meningitis (NTM) are discussed in this review and aid in accurate diagnosis. The intricate interplay of reactive oxygen species, ferroptosis, and reactive nitrogen species within the central nervous system reveals a promising field of research for innovative therapeutic strategies tailored to TBM. This review highlights the alternative treatments targeting oxidative stress-induced TBM and ferroptosis, providing potential avenues for intervention in the pathogenesis of this complex condition.
Insights
Tuberculous meningitis (TBM) involves oxidative stress and ferroptosis in the central nervous system. Research into these mechanisms offers new therapeutic strategies for TBM treatment.
Area of Science:
- Neuroscience
- Infectious Diseases
- Pathology
Background:
- Meningitis is inflammation of the meninges, caused by infectious or non-infectious agents.
- Central nervous system impact includes blood-brain barrier disruption and cellular changes.
- Differentiating tuberculous meningitis (TBM) from non-tuberculous meningitis (NTM) is crucial for diagnosis.
Purpose of the Study:
- To review clinical features differentiating TBM and NTM.
- To explore the role of reactive oxygen species, ferroptosis, and reactive nitrogen species in TBM.
- To highlight alternative treatments targeting oxidative stress and ferroptosis in TBM.
Main Methods:
- Literature review of clinical features and pathogenesis of TBM.
- Analysis of the interplay between oxidative stress, ferroptosis, and TBM.
- Identification of novel therapeutic targets for TBM.
Main Results:
- Clinical features aiding TBM diagnosis are discussed.
- Reactive oxygen species, ferroptosis, and reactive nitrogen species are implicated in TBM pathogenesis.
- Targeting these pathways presents potential therapeutic avenues.
Conclusions:
- Understanding the molecular mechanisms of TBM is key for developing new treatments.
- Therapeutic strategies focusing on oxidative stress and ferroptosis show promise for TBM.
- Further research into these pathways could lead to innovative interventions for TBM.
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