In vivo and in vitro neuroprotective effects of maca polysaccharide

Front Biosci (Landmark Ed). 2022 Jan 6;27(1):8. doi: 10.31083/j.fbl2701008.

Abstract

Objective: To explore the protective effect of MP on oxidative damage in vivo and in vitro.

Methods: A mouse aging model was induced by intraperitoneal injection of D-galactose (D-gal), and pathological changes in the hippocampal ultrastructure were observed by transmission electron microscopy. The activity of glutathione peroxidase (GSH-Px) and the levels of malondialdehyde (MDA) in brain tissues were evaluated with GSH-Px and MDA assay kits. An MTT assay was used to detect the viability of the model SH-SY5Y cells with H2O2-induced damage, and a lactate dehydrogenase (LDH) kit was used to evaluate LDH leakage. Reactive oxygen species (ROS) levels and cell cycle arrest were analyzed by flow cytometry, and cleaved caspase 3 and P53 protein expression was determined by western blot analysis.

Results: Demonstrated that MP increased GSH-Px activity, reduced MDA levels, and attenuated the cell damage induced by H2O2. Furthermore, MP protected neuronal cells from oxidative stress through a mechanism including a decrease in LDH leakage and reversal of H2O2-induced cell morphological damage. MP treatment alleviated the H2O2-induced increases in ROS levels, inhibited apoptosis, relieved cell cycle arrest, and downregulated cleaved caspase 3 and P53 protein expression.

Conclusions: MP is a novel antioxidant with neuroprotective effects.

Keywords: D-galactose; MP; Neuroprotective effect; Reactive oxygen species; SH-SY5Y cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Survival
  • Hydrogen Peroxide / toxicity
  • Lepidium* / metabolism
  • Mice
  • Neuroprotective Agents* / pharmacology
  • Oxidative Stress
  • Polysaccharides / pharmacology
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase / metabolism

Substances

  • Neuroprotective Agents
  • Polysaccharides
  • Reactive Oxygen Species
  • Hydrogen Peroxide
  • Superoxide Dismutase