Aug 2026· European Journal of Pharmacology· pp.
179274
· 0 citations· 144 references
Medicine
TL;DR
Targeting the crosstalk between neurogenesis and angiogenesis represents a promising preclinical approach for precise therapeutic intervention and holds potential to address some of the current clinical limitations and improve neurological functional recovery and long-term quality of life in patients with ischemic stroke, pending rigorous validation in future clinical studies.
Abstract
Stroke is a cerebrovascular disorder characterized by focal or global cerebral tissue damage, which ranks among the leading causes of mortality and disability globally. Ischemic stroke accounts for approximately 65.3% of all stroke cases. Currently, therapeutic strategies for ischemic stroke remain suboptimal. The concept of the neurovascular unit emphasizes the integrated regulation of neural and vascular components, and neurogenesis and angiogenesis represent the core neurovascular responses during ischemic stroke recovery. These two processes exhibit intimate crosstalk, forming a neurovascular collaborative repair mechanism that is precisely regulated by multiple cytokines and key signaling pathways. This review systematically summarizes the underlying mechanisms of this crosstalk and its pivotal role in post-stroke tissue repair and neurological functional recovery. Despite significant advances in this field, current research still has notable limitations, including insufficient elucidation of the interactions among multiple factors and pathways, unclear dynamic patterns of crosstalk across different recovery stages, and a lack of correlation between preclinical animal models and clinical scenarios. Future investigations should employ advanced technologies (e.g., single-cell sequencing) to further explore crosstalk mechanisms, focus on crosstalk associated with neural cell transdifferentiation, and establish preclinical models that closely mimic clinical conditions. Targeting the crosstalk between neurogenesis and angiogenesis represents a promising preclinical approach for precise therapeutic intervention. Although current evidence is largely derived from animal models, this strategy holds potential to address some of the current clinical limitations and improve neurological functional recovery and long-term quality of life in patients with ischemic stroke, pending rigorous validation in future clinical studies.
Novel communication modalities, specifically exosomes, which shuttle miRNAs and proteins to modulate distal inflammation, and Tunneling Nanotubes, which facilitate the direct intercellular transfer of vital organelles, such as mitochondria are highlighted.
Zhe Shen, Wei Wang, Dong-Dong Shi· Current Neuropharmacology· 0 citations
Examining microglial patterns in chronically injured tissue is examined to provide foundational insight into how regenerative gene therapy may influence the long-term neuroimmune environment after stroke.
BACKGROUND
Stroke remains a leading cause of disability and mortality worldwide. Although reperfusion therapy has improved clinical outcomes in the acute phase, long-term functional recovery remains limited. Neuroplasticity, a fundamental basis for functional recovery, is increasingly recognized as a multicellular inte...
Qian Zhang, Jia-Xu Liu, Shan-Ting Lu et al.· Phytomedicine· 0 citations
INTRODUCTION
Ischemic stroke remains a leading cause of disability and mortality worldwide. Current neuroprotective treatments predominantly target neurons and fail to address the complex post-ischemic cell death cascades in astrocytes, the most abundant glial cells in the central nervous system, whose multimodal Progr...
Li Zhang, Yong-Lan Ruan· Current Neurovascular Resear...· 0 citations
Ischemic stroke is a leading cause of permanent neurological disability worldwide, primarily driven by neuronal injury mechanisms such as excitotoxicity and oxidative stress. Consequently, understanding the molecular basis of post-ischemic neural repair has emerged as a critical focus in translational neuroscience. Acc...