Sesamol Attenuates Scopolamine-Induced Cholinergic Disorders, Neuroinflammation, and Cognitive Deficits in Mice.
Duo YunYajie WangYuyu ZhangMengzhen JiaTianzhi XieYihang ZhaoCong YangWeixuan ChenRui GuoXuebo LiuXiaoshuang DaiZhigang LiuTian YuanPublished in: Journal of agricultural and food chemistry (2022)
Alzheimer's disease (AD) is a neurodegenerative disease, characterized by memory loss and cognitive deficits accompanied by neuronal damage and cholinergic disorders. Sesamol, a lignan component in sesame oil, has been proven to have neuroprotective effects. This research aimed to investigate the preventive effects of sesamol on scopolamine (SCOP)-induced cholinergic disorders in C57BL/6 mice. The mice were pretreated with sesamol (100 mg/kg/d, p.o.) for 30 days. Behavioral tests indicated that sesamol supplement prevented SCOP-induced cognitive deficits. Sesamol enhanced the expression of neurotrophic factors and postsynaptic density (PSD) in SCOP-treated mice, reversing neuronal damage and synaptic dysfunction. Importantly, sesamol could balance the cholinergic system by suppressing the AChE activity and increasing the ChAT activity and M1 mAChR expression. Sesamol treatment also inhibited the expression of inflammatory factors and overactivation of microglia in SCOP-treated mice. Meanwhile, sesamol improved the antioxidant enzyme activity and suppressed oxidative stress in SCOP-treated mice and ameliorated the oxidized cellular status and mitochondrial dysfunction in SCOP-treated SH-SY5Y cells. In conclusion, these results indicated that sesamol attenuated SCOP-induced cognitive dysfunction via balancing the cholinergic system and reducing neuroinflammation and oxidative stress.
Keyphrases
- oxidative stress
- diabetic rats
- high fat diet induced
- high glucose
- poor prognosis
- induced apoptosis
- traumatic brain injury
- dna damage
- ischemia reperfusion injury
- wild type
- cognitive impairment
- inflammatory response
- spinal cord injury
- type diabetes
- endothelial cells
- cerebral ischemia
- insulin resistance
- long non coding rna
- cell death
- neuropathic pain
- binding protein
- adipose tissue
- spinal cord
- cell proliferation
- combination therapy
- cell cycle arrest
- anti inflammatory
- heat shock
- heat shock protein