Medical Physiology Department, Medical Research and Clinical Studies Institute, National Research Centre, Giza, Egypt.
Biophysics Department, Faculty of Science, Cairo University, Giza, Egypt.
Physiol Behav. 2024 Dec 1;287:114697. doi: 10.1016/j.physbeh.2024.114697. Epub 2024 Sep 15.
The therapeutic effects of alpha lipoic acid (LA) and/or caffeine-loaded chitosan nanoparticles (CCNPs) on obesity-induced memory impairment were evaluated in the present study. Rats were divided into control rats, obese rats induced by high fat diet (HFD) and obese rats treated with LA and/or CCNPs. Obesity was confirmed by measuring the body mass index (BMI). Memory and cognitive functions were evaluated by novel object recognition test (NORT). The levels of serotonin (5-HT), dopamine (DA), norepinephrine (NE), lipid peroxidation (MDA), nitric oxide (NO), reduced glutathione (GSH), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), leptin (LEP) and ghrelin (GHR) and the activities of monoamine oxidase (MAO), acetylcholinesterase (AchE) and Na,K,ATPase were determined in the cortex and hippocampus. The cerebral histopathological alterations were examined in obese rats. Obese rats showed impaired memory and exhibited significant neurochemical changes, including decreased levels of 5-HT, DA, GSH, GHR, and Na,K-ATPase activity, as well as an increase in AchE, MAO, MDA, NO, IL-1β, TNF-α, and LEP. LA and/or CCNPs treatment reduced BMI and improved memory. LA or CCNPs alleviated the cortical and hippocampal neurochemical changes and histopathological changes induced by obesity. Furthermore, LA and CCNPs exhibited antioxidant and anti-inflammatory properties, which likely contributed to their effects. However, no synergistic effect was observed between LA and CCNPs. These findings suggest that LA or CCNPs may be a potential therapy against obesity and its adverse effects on memory, mediated by their ability to restore monoamine levels and exhibit antioxidant and anti-inflammatory properties.
本研究评估了α-硫辛酸(LA)和/或载咖啡因壳聚糖纳米粒(CCNPs)对肥胖诱导的记忆障碍的治疗效果。将大鼠分为对照组、高脂肪饮食(HFD)诱导的肥胖组和用 LA 和/或 CCNPs 治疗的肥胖组。通过测量体重指数(BMI)来确认肥胖。通过新物体识别测试(NORT)评估记忆和认知功能。测定皮质和海马中 5-羟色胺(5-HT)、多巴胺(DA)、去甲肾上腺素(NE)、脂质过氧化(MDA)、一氧化氮(NO)、还原型谷胱甘肽(GSH)、白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、瘦素(LEP)和胃饥饿素(GHR)的水平以及单胺氧化酶(MAO)、乙酰胆碱酯酶(AchE)和 Na,K,ATPase 的活性。检查肥胖大鼠的大脑组织病理学改变。肥胖大鼠表现出记忆受损,并表现出明显的神经化学变化,包括 5-HT、DA、GSH、GHR 和 Na,K-ATPase 活性降低,AchE、MAO、MDA、NO、IL-1β、TNF-α和 LEP 增加。LA 和/或 CCNPs 治疗降低了 BMI 并改善了记忆。LA 或 CCNPs 减轻了肥胖引起的皮质和海马神经化学变化和组织病理学变化。此外,LA 和 CCNPs 具有抗氧化和抗炎特性,这可能是它们发挥作用的原因。然而,LA 和 CCNPs 之间没有观察到协同作用。这些发现表明,LA 或 CCNPs 可能是一种潜在的治疗肥胖及其对记忆的不良影响的疗法,其通过恢复单胺水平并表现出抗氧化和抗炎特性来发挥作用。