Therapeutic Effects of High-Intensity Interval Training Exercise Alone and Its Combination with Ecdysterone Against Amyloid Beta-Induced Rat Model of Alzheimer's Disease: A Behavioral, Biochemical, and Histological Study

被引:21
|
作者
Gholipour, Parsa [1 ,2 ]
Komaki, Alireza [2 ]
Parsa, Hesam [1 ]
Ramezani, Mahdi [3 ]
机构
[1] Bu Ali Sina Univ, Fac Sport Sci, Dept Exercise Physiol, Hamadan, Hamadan, Iran
[2] Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Hamadan, Iran
[3] Hamadan Univ Med Sci, Sch Med, Dept Anat, Hamadan, Hamadan, Iran
关键词
beta-Amyloid (A beta); Alzheimer's disease (AD); Ecdysterone; High Intensity Interval Training (HIIT); Learning; Oxidative stress; HIPPOCAMPAL SYNAPTIC PLASTICITY; OXIDATIVE STRESS; MITOCHONDRIAL DYSFUNCTION; NEUROTROPHIC FACTORS; COGNITIVE FUNCTION; MEMORY IMPAIRMENT; MOUSE MODEL; 20-HYDROXYECDYSONE; ANXIETY; MICE;
D O I
10.1007/s11064-022-03603-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hippocampal oxidative stress has a vital role in the pathophysiology of Alzheimer's disease (AD)-associated behavioral deficits. Ecdysterone (Ecdy), a natural product and primary steroid hormone, exhibits anti-oxidative and neuroprotective effects. High-intensity interval training (HIIT) has emerged as an effective method for improving physiological brain functions. The present study was designed to investigate the comparative effects of separate and combined HIIT and Ecdy treatment on behavioral functions, hippocampal oxidative status, histological changes in an amyloid-beta (A beta)-induced rat model of AD. Adult male rats were treated simultaneously with HIIT exercise and Ecdy (10 mg/kg/day; P.O.), starting ten days after A beta-injection, and they continued for eight consecutive weeks. At the end of the treatment course, the behavioral functions of the rats were assessed by commonly-used behavioral paradigms. Subsequently, brain samples were collected for histological analysis and hippocampus samples were collected for biochemical analysis. Results illustrated that Ap injection impaired learning and memory performances in both novel object recognition and Barnes maze tests, reduced exploratory/locomotor activities in open field test, enhanced anxiety-like behavior in elevated plus-maze (P < 0.05). These behavioral deficits accompanied hippocampal oxidative stress (decreased total antioxidant capacity content and glutathione peroxidase enzyme activity, increased total oxidant status and malondialdehyde level) and neuronal loss in the cerebral cortex and hippocampus in H&E staining (P <0.05). HIIT and Ecdy improved anxiety-like behavior, attenuated total oxidant status and malondialdehyde, and prevented the neuronal loss (P < 0.05). However, their combination resulted in a more complete and powerful improvement in all the above-mentioned Ap-related deficits (P < 0.05). Overall, these data provide evidence that a combination of HIIT and Ecdy treatment improves A beta-induced behavioral deficits, possibly through ameliorating hippocampal oxidative status and preventing neuronal loss.
引用
收藏
页码:2090 / 2108
页数:19
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