Protection against stroke with glucagon-like peptide-1 receptor agonists: a comprehensive review of potential mechanisms

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作者
Bruno Vergès
Victor Aboyans
Denis Angoulvant
Pierre Boutouyrie
Bertrand Cariou
Fabien Hyafil
Kamel Mohammedi
Pierre Amarenco
机构
[1] University of Burgundy,Department of Endocrinology, Diabetes and Metabolic Disorders, Dijon University Hospital, INSERM Unit, LNC
[2] Dupuytren University Hospital,UMR 1231
[3] Limoges University,Department of Cardiology, EpiMaCT
[4] University of Tours, INSERM UMR
[5] Tours University Hospital,EA4245 Transplantation, Immunity & Inflammation, Department of Cardiology
[6] INSERM,Paris Cardiovascular Research CenterUMR
[7] Georges-Pompidou European Hospital,970Department of Pharmacology
[8] Paris City University,Department of Nuclear Medicine, DMU IMAGINA
[9] University of Nantes,Department of Endocrinology, Diabetes, and Nutrition
[10] Nantes University Hospital Centre,Neurology and Stroke Center, SOS
[11] CNRS,TIA Clinic
[12] INSERM,undefined
[13] L’institut du Thorax,undefined
[14] Georges-Pompidou European Hospital,undefined
[15] APHP,undefined
[16] Paris City University,undefined
[17] University of Bordeaux,undefined
[18] INSERM U1034,undefined
[19] Bichat Hospital,undefined
[20] University of Paris,undefined
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关键词
Stroke; Glucagon-like peptide-1 receptor agonists; GLP-1; Neuroprotection; Mechanisms;
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摘要
Several randomized controlled trials have demonstrated the benefits of glucagon-like peptide-1 receptor agonists (GLP-1RAs) on ischemic stroke in patients with diabetes. In this review, we summarize and discuss the potential mechanisms of stroke protection by GLP-1RAs. GLP-1RAs exert multiple anti-atherosclerotic effects contributing to stroke prevention such as enhanced plaque stability, reduced vascular smooth muscle proliferation, increased nitric oxide, and improved endothelial function. GLP-1RAs also lower the risk of stroke by reducing traditional stroke risk factors including hyperglycemia, hypertension, and dyslipidemia. Independently of these peripheral actions, GLP-1RAs show direct cerebral effects in animal stroke models, such as reduction of infarct volume, apoptosis, oxidative stress, neuroinflammation, excitotoxicity, blood–brain barrier permeability, and increased neurogenesis, neuroplasticity, angiogenesis, and brain perfusion. Despite these encouraging findings, further research is still needed to understand more thoroughly the mechanisms by which GLP-1RAs may mediate stroke protection specifically in the human diabetic brain.
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