Journal
MOLECULES
Volume 27, Issue 18, Pages -Publisher
MDPI
DOI: 10.3390/molecules27185888
Keywords
acetylcholinesterase; choline acetyltransferase; neuroprotective; rosiridin
Funding
- Deanship of Scientific Research at Jouf University [DSR2022-RG-0150]
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The aim of this study was to determine whether rosiridin, a bioactive component of Rhodiola rosea, could protect rats from neurocognitive problems induced by scopolamine. The results showed that rosiridin improved behavioral parameters, reduced oxidative stress and inflammation markers, restored acetylcholine esterase and choline acetyltransferase activities, and normalized other biochemical parameters. These findings suggest that rosiridin may limit the effects of scopolamine on rat cognitive function.
Aim: A monoterpene and bioactive component of the plant Rhodiola rosea (R. rosea), rosiridin has beneficial effects on the human central nervous system and enhances brain function. The goal of this scientific study was to determine if rosiridin might shield rats from neurocognitive problems induced by scopolamine. Methods: To track the potential toxicities in rats, the acute toxicity in rats was clarified. Rosiridin at a dose of 10 mg/kg was tested in rats for 14 days. At the conclusion of the investigation, behavioral parameters that were used to identify the rats' cognitive and motor abilities were evaluated. Several biochemical parameters were estimated using the prepared homogenate, including acetylcholine esterase (AChE), choline acetyltransferase (ChAT), radical scavengers produced by the body (Catalase-CAT, superoxide dismutase-SOD, and reduced glutathione-GSH), indicators of oxidative and nitrative burnout, pro-inflammatory (Interleukins-IL-1 beta, IL-6, interferon gamma IFN-gamma, and tumor necrosis factor-TNF-alpha), and cell apoptosis caspases 3 and 9. Results and Conclusion: A significant behavioral parameter restoration was seen in the rosiridin-treated group, including reduction in latency time during acquisition and retention trial in the Morris water maze test, and percentage of spontaneous alterations in the y-maze test, when compared to the disease control group that received scopolamine; rosiridin also altered the oxidative stress and neuroinflammatory markers, as well as restoring Ach and ChAT activities and normalizing GSH, SOD, MDA, TNF-alpha, nitrate, IL-1 beta, IL-6, IFN-gamma, caspases 3 and 9 levels. The results imply that rosiridin limits the effect of scopolamine on rat cognitive function.
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