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Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke

Stroke is the second-leading cause of death and a leading cause of serious long-term disability worldwide, with an increasing global burden due to the growing and aging population. However, strict eligibility criteria for current treatment opportunities make novel therapeutic approaches desirable. O...

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Detalles Bibliográficos
Autores principales: Bereczki, Daniel, Balla, Jozsef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302555/
https://www.ncbi.nlm.nih.gov/pubmed/30014798
http://dx.doi.org/10.2174/1381612824666180717101104
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author Bereczki, Daniel
Balla, Jozsef
Bereczki, Daniel
author_facet Bereczki, Daniel
Balla, Jozsef
Bereczki, Daniel
author_sort Bereczki, Daniel
collection PubMed
description Stroke is the second-leading cause of death and a leading cause of serious long-term disability worldwide, with an increasing global burden due to the growing and aging population. However, strict eligibility criteria for current treatment opportunities make novel therapeutic approaches desirable. Oxi-dative stress plays a pivotal role during cerebral ischemia, eventually leading to neuronal injury and cell death. The significant correlation between redox imbalance and ischemic stroke has led to various treat-ment strategies targeting the endogenous antioxidant system in order to ameliorate the adverse prognosis in patients with cerebral infarction. One of the most extensively investigated cellular defense pathway in this regard is the Nrf2-heme oxygenase-1 (HO-1) axis. In this review, our aim is to focus on the poten-tial clinical relevance of targeting the HO-1 pathway in ischemic stroke.
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spelling pubmed-63025552019-01-14 Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke Bereczki, Daniel Balla, Jozsef Bereczki, Daniel Curr Pharm Des Article Stroke is the second-leading cause of death and a leading cause of serious long-term disability worldwide, with an increasing global burden due to the growing and aging population. However, strict eligibility criteria for current treatment opportunities make novel therapeutic approaches desirable. Oxi-dative stress plays a pivotal role during cerebral ischemia, eventually leading to neuronal injury and cell death. The significant correlation between redox imbalance and ischemic stroke has led to various treat-ment strategies targeting the endogenous antioxidant system in order to ameliorate the adverse prognosis in patients with cerebral infarction. One of the most extensively investigated cellular defense pathway in this regard is the Nrf2-heme oxygenase-1 (HO-1) axis. In this review, our aim is to focus on the poten-tial clinical relevance of targeting the HO-1 pathway in ischemic stroke. Bentham Science Publishers 2018-06 2018-06 /pmc/articles/PMC6302555/ /pubmed/30014798 http://dx.doi.org/10.2174/1381612824666180717101104 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Bereczki, Daniel
Balla, Jozsef
Bereczki, Daniel
Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke
title Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke
title_full Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke
title_fullStr Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke
title_full_unstemmed Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke
title_short Heme Oxygenase-1: Clinical Relevance in Ischemic Stroke
title_sort heme oxygenase-1: clinical relevance in ischemic stroke
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302555/
https://www.ncbi.nlm.nih.gov/pubmed/30014798
http://dx.doi.org/10.2174/1381612824666180717101104
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