Exploring the therapeutic implications of natural compounds modulating apoptosis in vascular dementia

Vascular dementia (VaD) is a prevalent form of dementia stemming from cerebrovascular disease, manifesting in memory impairment and executive dysfunction, thereby imposing a substantial societal burden. Unfortunately, no drugs have been approved for the treatment of VaD due to its intricate pathogen...

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Veröffentlicht in:Phytotherapy research 2024-11, Vol.38 (11), p.5270-5289
Hauptverfasser: Zhong, Guangcheng, Wang, Xinyue, Zhang, Qian, Zhang, Xueying, Fang, Xiaoling, Li, Shuting, Pan, Yaru, Ma, Yujie, Wang, Xuejing, Wan, Ting, Wang, Qi
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Sprache:eng
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Zusammenfassung:Vascular dementia (VaD) is a prevalent form of dementia stemming from cerebrovascular disease, manifesting in memory impairment and executive dysfunction, thereby imposing a substantial societal burden. Unfortunately, no drugs have been approved for the treatment of VaD due to its intricate pathogenesis, and the development of innovative and efficacious medications is urgently needed. Apoptosis, a programmed cell death process crucial for eliminating damaged or unwanted cells within an organism, assumes pivotal roles in embryonic development and tissue homeostasis maintenance. An increasing body of evidence indicates that apoptosis may significantly influence the onset and progression of VaD, and numerous natural compounds have demonstrated significant therapeutic potential. Here, we discuss the molecular mechanisms underlying apoptosis and its correlation with VaD. We also provide a crucial reference for developing innovative pharmaceuticals by systematically reviewing the latest research progress concerning the neuroprotective effects of natural compounds on VaD by regulating apoptosis. Further high‐quality clinical studies are imperative to firmly ascertain these natural compounds' clinical efficacy and safety profiles in the treatment of VaD. Natural compounds exert neuroprotective effects in vascular dementia by modulating apoptosis.
ISSN:0951-418X
1099-1573
1099-1573
DOI:10.1002/ptr.8316