Therapeutic effects of alpha lipoic acid and/or caffeine-loaded chitosan nanoparticles on memory impairment and neurochemical changes in high-fat diet-induced obese rats.
Study Goal
The researchers aimed to evaluate the therapeutic effects of Alpha-Lipoic Acid (LA) on obesity-induced memory impairment and neurochemical changes in rats.
Results Summary
LA treatment improved memory, reduced BMI, and alleviated neurochemical and histopathological changes in obese rats, demonstrating antioxidant and anti-inflammatory properties. No synergistic effect was observed between LA and caffeine-loaded chitosan nanoparticles (CCNPs).
Population
Obese rats induced by a high-fat diet.
Effective Dosage
Not specified
Duration
Not specified
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
alpha lipoic acid (LA) and/or caffeine-loaded chitosan nanoparticles (CCNPs) | neutral | therapeutic effects on obesity-induced memory impairment | rats | - | evaluated | #1 |
high fat diet (HFD) | increase | obesity | rats | - | induced | #2 |
high fat diet (HFD) | decrease | impaired memory | obese rats | - | showed | #3 |
high fat diet (HFD) | decrease | levels of serotonin (5-HT) | obese rats | - | exhibited | #4 |
high fat diet (HFD) | decrease | levels of dopamine (DA) | obese rats | - | exhibited | #5 |
high fat diet (HFD) | decrease | levels of reduced glutathione (GSH) | obese rats | - | exhibited | #6 |
high fat diet (HFD) | decrease | levels of ghrelin (GHR) | obese rats | - | exhibited | #7 |
high fat diet (HFD) | decrease | Na+,K+-ATPase activity | obese rats | - | exhibited | #8 |
high fat diet (HFD) | increase | acetylcholinesterase (AchE) | obese rats | - | exhibited | #9 |
high fat diet (HFD) | increase | monoamine oxidase (MAO) | obese rats | - | exhibited | #10 |
high fat diet (HFD) | increase | lipid peroxidation (MDA) | obese rats | - | exhibited | #11 |
high fat diet (HFD) | increase | nitric oxide (NO) | obese rats | - | exhibited | #12 |
high fat diet (HFD) | increase | interleukin-1β (IL-1β) | obese rats | - | exhibited | #13 |
high fat diet (HFD) | increase | tumor necrosis factor-α (TNF-α) | obese rats | - | exhibited | #14 |
high fat diet (HFD) | increase | leptin (LEP) | obese rats | - | exhibited | #15 |
LA and/or CCNPs treatment | decrease | BMI | obese rats | - | reduced | #16 |
LA and/or CCNPs treatment | increase | memory | obese rats | - | improved | #17 |
LA or CCNPs | decrease | cortical and hippocampal neurochemical changes | obese rats | - | alleviated | #18 |
LA or CCNPs | decrease | histopathological changes | obese rats | - | alleviated | #19 |
LA and CCNPs | increase | antioxidant properties | - | - | exhibited | #20 |
LA and CCNPs | increase | anti-inflammatory properties | - | - | exhibited | #21 |
LA and CCNPs | no change | effects | - | - | no synergistic effect was observed | #22 |
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.