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The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies

Background: Delayed cerebral vasospasm (DCVS) due to aneurysmal subarachnoid hemorrhage (aSAH) and its sequela, delayed cerebral ischemia (DCI), are associated with poor functional outcome. Endothelin-1 (ET-1) is known to play a major role in mediating cerebral vasoconstriction. Angiotensin-II-type-...

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Autores principales: Wanderer, Stefan, Grüter, Basil E., Strange, Fabio, Sivanrupan, Sivani, Di Santo, Stefano, Widmer, Hans Rudolf, Fandino, Javier, Marbacher, Serge, Andereggen, Lukas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139942/
https://www.ncbi.nlm.nih.gov/pubmed/32156050
http://dx.doi.org/10.3390/brainsci10030153
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author Wanderer, Stefan
Grüter, Basil E.
Strange, Fabio
Sivanrupan, Sivani
Di Santo, Stefano
Widmer, Hans Rudolf
Fandino, Javier
Marbacher, Serge
Andereggen, Lukas
author_facet Wanderer, Stefan
Grüter, Basil E.
Strange, Fabio
Sivanrupan, Sivani
Di Santo, Stefano
Widmer, Hans Rudolf
Fandino, Javier
Marbacher, Serge
Andereggen, Lukas
author_sort Wanderer, Stefan
collection PubMed
description Background: Delayed cerebral vasospasm (DCVS) due to aneurysmal subarachnoid hemorrhage (aSAH) and its sequela, delayed cerebral ischemia (DCI), are associated with poor functional outcome. Endothelin-1 (ET-1) is known to play a major role in mediating cerebral vasoconstriction. Angiotensin-II-type-1-receptor antagonists such as Sartans may have a beneficial effect after aSAH by reducing DCVS due to crosstalk with the endothelin system. In this review, we discuss the role of Sartans in the treatment of stroke and their potential impact in aSAH. Methods: We conducted a literature research of the MEDLINE PubMed database in accordance with PRISMA criteria on articles published between 1980 to 2019 reviewing: “Sartans AND ischemic stroke”. Of 227 studies, 64 preclinical and 19 clinical trials fulfilled the eligibility criteria. Results: There was a positive effect of Sartans on ischemic stroke in both preclinical and clinical settings (attenuating ischemic brain damage, reducing cerebral inflammation and infarct size, increasing cerebral blood flow). In addition, Sartans reduced DCVS after aSAH in animal models by diminishing the effect of ET-1 mediated vasoconstriction (including cerebral inflammation and cerebral epileptogenic activity reduction, cerebral blood flow autoregulation restoration as well as pressure-dependent cerebral vasoconstriction). Conclusion: Thus, Sartans might play a key role in the treatment of patients with aSAH.
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spelling pubmed-71399422020-04-13 The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies Wanderer, Stefan Grüter, Basil E. Strange, Fabio Sivanrupan, Sivani Di Santo, Stefano Widmer, Hans Rudolf Fandino, Javier Marbacher, Serge Andereggen, Lukas Brain Sci Review Background: Delayed cerebral vasospasm (DCVS) due to aneurysmal subarachnoid hemorrhage (aSAH) and its sequela, delayed cerebral ischemia (DCI), are associated with poor functional outcome. Endothelin-1 (ET-1) is known to play a major role in mediating cerebral vasoconstriction. Angiotensin-II-type-1-receptor antagonists such as Sartans may have a beneficial effect after aSAH by reducing DCVS due to crosstalk with the endothelin system. In this review, we discuss the role of Sartans in the treatment of stroke and their potential impact in aSAH. Methods: We conducted a literature research of the MEDLINE PubMed database in accordance with PRISMA criteria on articles published between 1980 to 2019 reviewing: “Sartans AND ischemic stroke”. Of 227 studies, 64 preclinical and 19 clinical trials fulfilled the eligibility criteria. Results: There was a positive effect of Sartans on ischemic stroke in both preclinical and clinical settings (attenuating ischemic brain damage, reducing cerebral inflammation and infarct size, increasing cerebral blood flow). In addition, Sartans reduced DCVS after aSAH in animal models by diminishing the effect of ET-1 mediated vasoconstriction (including cerebral inflammation and cerebral epileptogenic activity reduction, cerebral blood flow autoregulation restoration as well as pressure-dependent cerebral vasoconstriction). Conclusion: Thus, Sartans might play a key role in the treatment of patients with aSAH. MDPI 2020-03-07 /pmc/articles/PMC7139942/ /pubmed/32156050 http://dx.doi.org/10.3390/brainsci10030153 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wanderer, Stefan
Grüter, Basil E.
Strange, Fabio
Sivanrupan, Sivani
Di Santo, Stefano
Widmer, Hans Rudolf
Fandino, Javier
Marbacher, Serge
Andereggen, Lukas
The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies
title The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies
title_full The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies
title_fullStr The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies
title_full_unstemmed The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies
title_short The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies
title_sort role of sartans in the treatment of stroke and subarachnoid hemorrhage: a narrative review of preclinical and clinical studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139942/
https://www.ncbi.nlm.nih.gov/pubmed/32156050
http://dx.doi.org/10.3390/brainsci10030153
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