Sheng Li Xue Bao. 2026 Apr 25;78(2):270-282. doi: 10.13294/j.aps.2025.0110.
ABSTRACT
Ischemic stroke is a common cerebrovascular disease with an increasing incidence year by year, and it remains one of the leading causes of death and disability worldwide. The β-adrenergic receptor (β-AR), a member of the G protein-coupled receptor (GPCR) family, functions on the cell membrane by binding to specific ligands such as epinephrine (E) and norepinephrine (NE), thereby regulating intracellular signal transduction. Recent studies have revealed that the β-AR signaling pathway exerts multifaceted neuroprotective effects on ischemic stroke, including promoting the secretion of neurotrophic factors, mitigating inflammatory responses, inhibiting apoptosis, reducing excitotoxicity, and repairing the blood-brain barrier. Furthermore, research suggests that β-AR activation plays a role in post-stroke pneumonia. Additionally, β-AR gene polymorphisms have been significantly associated with the risk of ischemic stroke. This article reviews the mechanisms of the β-AR signaling pathway in ischemic stroke, aiming to provide a theoretical foundation for the prevention and treatment of this condition.
PMID:42014327 | DOI:10.13294/j.aps.2025.0110