The Role of Sartans in the Treatment of Stroke and Subarachnoid Hemorrhage: A Narrative Review of Preclinical and Clinical Studies.
Stefan WandererBasil Erwin GrüterFabio StrangeSivani SivanrupanStefano Di SantoHans Rudolf WidmerJavier FandinoSerge MarbacherLukas AndereggenPublished in: Brain sciences (2020)
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.
Keyphrases
- subarachnoid hemorrhage
- cerebral ischemia
- brain injury
- cerebral blood flow
- blood brain barrier
- angiotensin ii
- clinical trial
- oxidative stress
- atrial fibrillation
- multiple sclerosis
- emergency department
- stem cells
- mesenchymal stem cells
- acute myocardial infarction
- heart failure
- ischemia reperfusion injury
- adverse drug
- randomized controlled trial
- cell therapy
- replacement therapy
- angiotensin converting enzyme
- vascular smooth muscle cells