Quispe-Díaz, IvánGrupo de Investigación en Estudios de Compuestos Naturales y Sintéticos con Actividad a Nivel Sistema Nervioso Central y Musculo Liso, Laboratorio de Farmacología, Facultad de Farmacia y Bioquímica, Universidad Nacional de Trujillo, Trujillo 13011, Peru
Author
Ybañez-Julca, RobertoGrupo de Investigación en Estudios de Compuestos Naturales y Sintéticos con Actividad a Nivel Sistema Nervioso Central y Musculo Liso, Laboratorio de Farmacología, Facultad de Farmacia y Bioquímica, Universidad Nacional de Trujillo, Trujillo 13011, Peru
Author
Asunción-Alvarez, DanielGrupo de Investigación en Estudios de Compuestos Naturales y Sintéticos con Actividad a Nivel Sistema Nervioso Central y Musculo Liso, Laboratorio de Farmacología, Facultad de Farmacia y Bioquímica, Universidad Nacional de Trujillo, Trujillo 13011, Peru
Author
Enriquez-Lara, CinthyaPrograma de Doctorado en Química Medicinal, Facultad de Ciencias de la Salud, Universidad Arturo Prat, Casilla 121, Iquique 1110939, Chile
Author
Buc Calderon, PedroUCLouvain
Author
Benites, JulioPrograma de Doctorado en Química Medicinal, Facultad de Ciencias de la Salud, Universidad Arturo Prat, Casilla 121, Iquique 1110939, Chile
Lepidium meyenii Walp. (black maca, BM) is a traditional Andean crop increasingly studied for its bioactive potential. This work characterized the phytochemical profile and evaluated the antioxidant, antinociceptive, and neuroprotective properties of a lyophilized aqueous extract of BM hypocotyls. UHPLC-ESI-QTOF-MS/MS identified twelve major compounds, including macamides, imidazole alkaloids, sterols, and fatty acid amides. BM showed a moderate total phenolic content but strong electron transfer-based antioxidant activity in CUPRAC and FRAP assays, together with moderate radical scavenging capacity in ABTS and DPPH systems. In ovariectomized rats, BM significantly reduced brain malondialdehyde levels, mitigated oxidative stress, and improved spatial learning during acquisition in the Morris water maze, confirming its neuroprotective effect. Antinociceptive assays (hot plate, cold plate, and tail immersion) further revealed a rapid but transient increase in nociceptive thresholds. This study provides experimental evidence supporting the analgesic effect of black maca. Molecular docking highlighted lepidiline B and campesterol as key metabolites with strong interactions with redox enzymes, the μ-opioid receptor, and the FAAH enzyme, supporting their role in the observed bioactivities. ADMET predictions indicated favorable oral bioavailability, CNS penetration, systemic clearance, and acceptable safety profiles. These results substantiate the role of black maca as a neuroprotective nutraceutical and highlight its promise as a novel source of rapidly acting natural analgesic compounds.
Quispe-Díaz, I., Ybañez-Julca, R., Asunción-Alvarez, D., Enriquez-Lara, C., Polo-Bardales, J., Jara-Aguilar, R., Venegas-Casanova, E., De Albuquerque, R., Costilla-Sánchez, N., Vásquez-Corales, E., Buc Calderon, P., & Benites, J. (2025). Antioxidant, Neuroprotective, and Antinociceptive Effects of Peruvian Black Maca (Lepidium meyenii Walp.). Antioxidants, 14(10), 1214 [1-22]. https://doi.org/10.3390/antiox14101214 (Original work published 2025)