Related Experiment Video
Updated: May 30, 2026

Murine Drinking Models in the Development of Pharmacotherapies for Alcoholism: Drinking in the Dark and Two-bottle Choice
Published on: January 7, 2019
Dose-response effect of black maca (Lepidium meyenii) in mice with memory impairment induced by ethanol
Julio Rubio1, Sandra Yucra, Manuel Gasco
1Department of Biological and Physiological Sciences, Faculty of Sciences and Philosophy and Instituto de Investigaciones de la Altura, Universidad Peruana Cayetano Heredia , Lima , Peru. julio.rubio.m@upch.pe
Abstract:
Previous studies have shown that black variety of maca has beneficial effects on learning and memory in experimental animal models. The present study aimed to determine whether the hydroalcoholic extract of black maca (BM) showed a dose-response effect in mice treated with ethanol 20% (EtOH) as a model of memory impairment. Mice were divided in the following groups: control, EtOH, ascorbic acid (AA) and 0.125, 0.25, 0.50 and 1.00 g/kg of BM plus EtOH. All treatments were orally administered for 28 days. Open field test was performed to determine locomotor activity and water Morris maze was done to determine spatial memory. Also, total polyphenol content in the hydroalcoholic extract of BM was determined (0.65 g pyrogallol/100 g). Mice treated with EtOH took more time to find the hidden platform than control during escape acquisition trials; meanwhile, AA and BM reversed the effect of EtOH. In addition, AA and BM ameliorated the deleterious effect of EtOH during the probe trial. Correlation analyses showed that the effect of BM a dose-dependent behavior. Finally, BM improved experimental memory impairment induced by ethanol in a dose-response manner due, in part, to its content of polyphenolic compounds.
Insights
Black maca extract (BM) improved ethanol-induced memory impairment in mice. This effect was dose-dependent and linked to its polyphenol content, suggesting potential cognitive benefits.
Area of Science:
- Neuroscience
- Pharmacology
- Ethnobotany
Background:
- Black maca (BM) shows promise for enhancing learning and memory in animal models.
- Ethanol (EtOH) consumption can impair cognitive functions, particularly memory.
- Polyphenolic compounds are known for their antioxidant and neuroprotective properties.
Purpose of the Study:
- To investigate the dose-response effects of hydroalcoholic black maca extract on ethanol-induced memory impairment in mice.
- To evaluate the impact of black maca on locomotor activity and spatial memory.
Main Methods:
- Mice were administered ethanol (20%) and varying doses of black maca extract (0.125–1.00 g/kg) or ascorbic acid for 28 days.
- Locomotor activity was assessed using the Open Field Test.
- Spatial memory was evaluated using the Water Morris Maze test.
- Total polyphenol content in the black maca extract was quantified.
Main Results:
- Ethanol-treated mice exhibited significant memory deficits compared to controls.
- Black maca extract, at all tested doses, reversed the memory impairment caused by ethanol.
- Ascorbic acid also demonstrated a protective effect against ethanol-induced memory deficits.
- Black maca extract improved performance in both escape acquisition and probe trials of the Water Morris Maze.
- The cognitive-enhancing effects of black maca were found to be dose-dependent.
- The hydroalcoholic extract of black maca contained 0.65 g pyrogallol/100 g of total polyphenols.
Conclusions:
- Hydroalcoholic extract of black maca effectively ameliorates experimental memory impairment induced by ethanol in a dose-dependent manner.
- The neuroprotective effects of black maca are, at least partially, attributable to its rich polyphenol content.
- Black maca presents a potential natural therapeutic agent for managing ethanol-induced cognitive deficits.
More Related Videos
05:12Chronic Intermittent Ethanol Vapor Exposure Paired with Two-Bottle Choice to Model Alcohol Use Disorder
Published on: June 23, 2023
07:50A Method for Evaluating the Reinforcing Properties of Ethanol in Rats without Water Deprivation, Saccharin Fading or Extended Access Training
Published on: January 29, 2017