The potential mechanism and clinical application value of remote ischemic conditioning in stroke.
Yajun ZhuXiaoguo LiXingwei LeiLiuyang TangDaochen WenBo ZengXiaofeng ZhangZichao HuangZongduo GuoPublished in: Neural regeneration research (2024)
Some studies have confirmed the neuroprotective effect of remote ischemic conditioning against stroke. Although numerous animal researches have shown that the neuroprotective effect of remote ischemic conditioning may be related to neuroinflammation, cellular immunity, apoptosis, and autophagy, the exact underlying molecular mechanisms are unclear. This review summarizes the current status of different types of remote ischemic conditioning methods in animal and clinical studies and analyzes their commonalities and differences in neuroprotective mechanisms and signaling pathways. Remote ischemic conditioning has emerged as a potential therapeutic approach for improving stroke-induced brain injury owing to its simplicity, non-invasiveness, safety, and patient tolerability. Different forms of remote ischemic conditioning exhibit distinct intervention patterns, timing, and application range. Mechanistically, remote ischemic conditioning can exert neuroprotective effects by activating the Notch1/phosphatidylinositol 3-kinase/Akt signaling pathway, improving cerebral perfusion, suppressing neuroinflammation, inhibiting cell apoptosis, activating autophagy, and promoting neural regeneration. While remote ischemic conditioning has shown potential in improving stroke outcomes, its full clinical translation has not yet been achieved.
Keyphrases
- cerebral ischemia
- signaling pathway
- brain injury
- subarachnoid hemorrhage
- blood brain barrier
- pi k akt
- ischemia reperfusion injury
- atrial fibrillation
- induced apoptosis
- oxidative stress
- cell death
- epithelial mesenchymal transition
- endoplasmic reticulum stress
- cell proliferation
- stem cells
- magnetic resonance
- case report
- metabolic syndrome
- type diabetes
- adipose tissue
- climate change
- computed tomography
- skeletal muscle
- risk assessment
- protein kinase
- insulin resistance
- diabetic rats
- lps induced
- double blind