Acetylcholine and memory-enhancing activity of Ficus racemosa bark

Alzheimer's disease (AD) is a progressive neurodegenerative disorder resulting in dementia and enhancement of acetylcholine (Ach) levels in brain using acetylcholinesterase inhibitors is one of the most important approaches for the treatment of AD. In this study, aqueous extract of Ficus racemo...

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Published in:Pharmacognosy research Vol. 3; no. 4; pp. 246 - 249
Main Authors: Ahmed, Faiyaz, Chandra, J N Narendra Sharath, Manjunath, S
Format: Journal Article
Language:English
Published: India Medknow Publications and Media Pvt. Ltd 01-10-2011
Phcog.net
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Summary:Alzheimer's disease (AD) is a progressive neurodegenerative disorder resulting in dementia and enhancement of acetylcholine (Ach) levels in brain using acetylcholinesterase inhibitors is one of the most important approaches for the treatment of AD. In this study, aqueous extract of Ficus racemosa Linn. (Moraceae) bark having anti-inflammatory, antioxidant, and anticholinesterase activity was evaluated for its ability to enhance Ach levels, and to ascertain its antidementia activity in rats. This work was carried out under the assumption that the F. racemosa extract may show combination of actions which could be beneficial in the treatment of AD, such as neuroprotection, attributed to antioxidant and anti-infl ammatory property and may elevate levels of Ach like Ficus hispida extract reported earlier. Administration of the extract at two levels viz., 250 and 500 mg/kg signifi cantly raised (P ≤ 0.05) Ach levels in hippocampi of rats compared to control. The percentage enhancement in Ach levels was found to be 22% and 38%, respectively. Further, the extract at both dosage levels elicited signifi cant reduction (P ≤ 0.05) in transfer latency on elevated plus-maze, which was used as an exteroceptive behavioral model to evaluate memory in rats. It is inferred that it would be worthwhile to explore the potential of F. racemosa in the management of Alzheimer disease.
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ISSN:0974-8490
0976-4836
0974-8490
DOI:10.4103/0974-8490.89744