Donepezil Improves PSD95 Expression, Mitigates Neuroinflammation via PI3K/Akt/NF‐κB and Mitochondrial Dysfunction in a Rodent Model of Subarachnoid Haemorrhage

多奈哌齐 神经保护 奶油 神经炎症 药理学 线粒体 化学 生物 内科学 内分泌学 医学 细胞生物学 生物化学 炎症 痴呆 疾病 基因 转录因子
作者
Ahmed Shaney Rehman,Ammar Tasleem,Nemat Ali,Rehan Khan,Mohd Salman,Pravir Kumar,Suhel Parvez
出处
期刊:Journal of Neurochemistry [Wiley]
卷期号:169 (4)
标识
DOI:10.1111/jnc.70063
摘要

ABSTRACT Mitochondrial dysfunction is a known contributor to subarachnoid haemorrhage (SAH) induced early brain damage (EBI), leading to poor neurological outcomes. An experimental SAH model was induced in adult male Wistar rats using endovascular perforation. Donepezil, an acetylcholinesterase (AChE) inhibitor (1 or 2 mg/kg body weight), was administered intraperitoneally 4 h after SAH. The severity of cerebral cortex injury was assessed using blood clot grading, behavioral tests and H and E staining. We carried out an assessment of neuroinflammatory markers using western blotting and immunofluorescence. Additionally, we examined neuronal architecture using H and E staining, measured mitochondrial redox imbalance or ROS and membrane potential (Δѱm) and analyzed mitochondrial morphology using transmission electron microscopy (TEM). Apoptotic markers and mitochondrial respiratory complexes were assessed by western blotting. Our results indicated that donepezil treatment significantly upregulated PSD95, α7‐AChR, CaMKII, BDNF, CREB, and PI3K expression in cerebral cortical neurons in response to SAH. This was accompanied by improved neurological function, reduced brain edema, decreased neuronal degeneration, and increased levels of OXPHOS and ATP. In the cerebral cortex, donepezil inhibited mitochondria‐associated neuronal apoptosis after SAH as revealed by increased membrane potential integrity of mitochondria, reducing the ratio of Bax to Bcl‐2 and inhibiting caspase‐3 activity. Additionally, donepezil upregulated synaptic proteins (PSD95), strengthening synaptic connections and supporting spatial working memory circuits via the neurotrophic factor BDNF in post‐SAH rats. Our research concludes that donepezil has neuroprotective benefits by inhibiting SAH‐induced mitochondrial‐mediated cell death through the regulation of Drp1‐mediated mitochondrial morphology changes. image

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