| Literature DB >> 29351721 |
Kanta Pravalika1, Deepaneeta Sarmah1, Harpreet Kaur1, Madhuri Wanve1, Jackson Saraf1, Kiran Kalia1, Anupom Borah2, Dileep R Yavagal3, Kunjan R Dave4, Pallab Bhattacharya1.
Abstract
Myeloperoxidase (MPO) is a protein present in azurophilic granules, macrophages, and neutrophils that are released into extracellular fluid (ECF) during inflammation. MPO releases hypochlorous acid (HOCl) and other chlorinated species. It is derived from hydrogen peroxide (H2O2) showing response during inflammatory conditions and plays a role in the immune defense against pathogens. MPO may show unwanted effects by indirectly increasing the formation of reactive nitrogen species (RNS), reactive oxygen species (ROS), and tumor necrosis factor alpha (TNF-α) leading to inflammation and oxidative stress. As neuroinflammation is one of the inevitable biological components among most of neurological disorders, MPO and its receptor may be explored as candidates for future clinical interventions. The purpose of this review is to provide an overview of the pathophysiological characteristics of MPO and further explore the possibilities to target it for clinical use. Targeting MPO is promising and may open an avenue to act as a biomarker for diagnosis with defined risk stratification in patients with various neurological disorders.Entities:
Keywords: Myeloperoxidase; neuroinflammation; neuroprotection
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Year: 2018 PMID: 29351721 DOI: 10.1021/acschemneuro.7b00462
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418