Deciphering mitochondrial dysfunction: Pathophysiological mechanisms in vascular cognitive impairment

Vascular cognitive impairment (VCI) encompasses a range of cognitive deficits arising from vascular pathology. The pathophysiological mechanisms underlying VCI remain incompletely understood; however, chronic cerebral hypoperfusion (CCH) is widely acknowledged as a principal pathological contributor...

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Published inBiomedicine & pharmacotherapy Vol. 174; p. 116428
Main Authors He, Yuyao, He, Tiantian, Li, Hongpei, Chen, Wei, Zhong, Biying, Wu, Yue, Chen, Runming, Hu, Yuli, Ma, Huaping, Wu, Bin, Hu, Wenyue, Han, Zhenyun
Format Journal Article
LanguageEnglish
Published France Elsevier Masson SAS 01.05.2024
Elsevier
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Summary:Vascular cognitive impairment (VCI) encompasses a range of cognitive deficits arising from vascular pathology. The pathophysiological mechanisms underlying VCI remain incompletely understood; however, chronic cerebral hypoperfusion (CCH) is widely acknowledged as a principal pathological contributor. Mitochondria, crucial for cellular energy production and intracellular signaling, can lead to numerous neurological impairments when dysfunctional. Recent evidence indicates that mitochondrial dysfunction—marked by oxidative stress, disturbed calcium homeostasis, compromised mitophagy, and anomalies in mitochondrial dynamics—plays a pivotal role in VCI pathogenesis. This review offers a detailed examination of the latest insights into mitochondrial dysfunction within the VCI context, focusing on both the origins and consequences of compromised mitochondrial health. It aims to lay a robust scientific groundwork for guiding the development and refinement of mitochondrial-targeted interventions for VCI.
Bibliography:ObjectType-Article-2
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ObjectType-Review-1
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2024.116428