摘要
Ischemia-reperfusion(I/R)injury induces region-specific neuronal vulnerability within the hippocampus,with the cornu ammonis 1(CA1)subfield particularly prone to delayed neuronal death.While intrinsic neuronal factors have been implicated,emerging evidence highlights the decisive contribution of astrocyte endfeet(AEF)—specialized perivascular structures that regulate ion and water homeostasis,glutamate clearance,and blood–brain barrier(BBB)stability.This review synthesizes structural and molecular alterations of AEF across the CA1-CA3 subfields following I/R and their correlation with neuronal fate.In CA1,AEF undergo early-onset swelling and detachment from the vascular basal lamina due to dysfunction of critical proteins such as aquaporin-4(AQP4)and Kir4.1.These changes impair glutamate uptake,metabolic support,and potassium buffering,contributing to neuronal hyperexcitability and degeneration.In contrast,AEF in CA3 preserves polarity and functional coupling of AQP4 and Kir4.1,conferring regional resilience.At the signaling level,AEF disruption activates mitogen-activated protein kinase(MAPK)/c-Jun N-terminal kinase(JNK)pathways,promotes reactive oxygen species(ROS)accumulation,and induces inducible nitric oxide synthase(iNOS)-mediated inflammation,amplifying neurotoxicity.Furthermore,subfield-specific astrocytic transcriptional profiles modulate inflammatory responses and gliovascular interactions.By reframing AEF not as passive scaffolds but as active regulators of neuronal survival,this review provides novel insight into the astrocyte-dependent mechanisms of hippocampal vulnerability.Therapeutic strategies that preserve AEF structure and function may offer targeted protection against delayed neuronal death in ischemic brain injury.
