7,8-Dihydroxyflavone improves cognitive functions in ICV-STZ rat model of sporadic Alzheimer's disease by reversing oxidative stress, mitochondrial dysfunction, and insulin resistance

被引:51
|
作者
Akhtar, Ansab [1 ]
Dhaliwal, Jatinder [1 ]
Sah, Sangeeta Pilkhwal [1 ]
机构
[1] Panjab Univ, Univ Inst Pharmaceut Sci, Div Pharmacol, Chandigarh 160014, India
关键词
ICV-STZ; 7; 8-Dihydroxyflavone; Sporadic Alzheimer’ s disease; Oxidative stress; Mitochondrial dysfunction; Insulin resistance; Cholinergic dysfunction; Tau pathology; Neurodegeneration; INDUCED-MEMORY IMPAIRMENT; MOUSE MODEL; TAU HYPERPHOSPHORYLATION; ELECTRON-TRANSPORT; B AGONIST; VITAMIN-E; STREPTOZOTOCIN; BRAIN; ACTIVATION; DEFICITS;
D O I
10.1007/s00213-021-05826-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale Intracerebroventricular (ICV) streptozotocin (STZ) mimics sporadic Alzheimer's disease (SAD) characterized by tau pathology and neurodegeneration arising from oxidative stress, mitochondrial dysfunction, and insulin resistance. 7,8-Dihydroxyflavone (7,8-DHF) is a flavonoid having antioxidant property interlinked with mitochondrial functioning and insulin actions. Objectives To evaluate the neuroprotective and cognitive enhancement properties of 7,8-DHF in an ICV-STZ rat model of SAD. Methods ICV-STZ (3 mg/kg) was injected into male Wistar rats. Cognitive functions were evaluated by Morris water maze (MWM) and novel object recognition (NOR). 7,8-DHF (5 mg/kg, 10 mg/kg, and 20 mg/kg) and rivastigmine (2 mg/kg) were given orally for 21 days. Reduced glutathione (GSH), catalase, superoxide dismutase (SOD), glutathione peroxidase (GPX), lipid peroxidation (LPO), protein carbonylation (PCO), and nitrite assays were performed. Mitochondrial enzyme complex I, II, III, and IV, and acetylcholinesterase (AchE) activities were determined. ELISA for the insulin-degrading enzyme (IDE) and p-tau was done. Histopathology was investigated by hematoxylin and eosin staining. Results 7,8-DHF treatment attenuated ICV-STZ-induced cognitive deficit in MWM and NOR. Moreover, in the cortex and hippocampus regions of the brain, GSH, catalase, SOD, GPX, LPO, PCO, and nitrite levels were reversed. Mitochondrial enzyme complex I, II, III, and IV, and acetylcholinesterase (AchE) activities were also normalized. IDE and p-tau protein were found to be significantly altered. 7,8-DHF provided protection from neuronal cell death examined in histopathology. Conclusions Conclusively, 7,8-DHF was found to be neuroprotective in the ICV-STZ rat model by ameliorating oxidative stress, mitochondrial dysfunction, and insulin resistance, thereby improving cognitive functions evident with the behavioral results.
引用
收藏
页码:1991 / 2009
页数:19
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