1-Methoxylespeflorin G11 Protects HT22 Cells from Glutamate-Induced Cell Death through Inhibition of ROS Production and Apoptosis

J Microbiol Biotechnol. 2021 Feb 28;31(2):217-225. doi: 10.4014/jmb.2011.11032.

Abstract

This study aimed to investigate the neuroprotective effects of 1-methoxylespeflorin G11 (MLG), a pterocarpan, against glutamate-induced neurotoxicity in neuronal HT22 hippocampal cells. The protective effects of MLG were evaluated using MTT assay and microscopic analysis. The extent of apoptosis was studied using flow cytometric analysis performed on the damaged cells probed with annexin V/propidium iodide. Moreover, mitochondrial reactive oxygen species (ROS) were assessed using flow cytometry through MitoSOXTM Red staining. To determine mitochondrial membrane potential, staining with tetramethylrhodamine and JC-1 was performed followed by flow cytometry. The results demonstrated that MLG attenuates glutamate-induced apoptosis in HT22 cells by inhibiting intracellular ROS generation and mitochondrial dysfunction. Additionally, MLG prevented glutamate-induced apoptotic pathway in HT22 cells through upregulation of Bcl-2 and downregulation of cleaved PARP-1, AIF, and phosphorylated MAPK cascades. In addition, MLG treatment induced HO-1 expression in HT22 cells. These results suggested that MLG exhibits neuroprotective effects against glutamate-induced neurotoxicity in neuronal HT22 cells by inhibiting oxidative stress and apoptosis.

Keywords: 1-Methoxylespeflorin G11; HT22 cells; apoptosis; mitochondrial membrane potential (MMP); reactive oxygen species (ROS).

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Cell Death / drug effects*
  • Cell Line
  • Glutamic Acid / toxicity
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Neurons / cytology
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neuroprotective Agents / pharmacology*
  • Oxidative Stress / drug effects
  • Poly (ADP-Ribose) Polymerase-1 / genetics
  • Poly (ADP-Ribose) Polymerase-1 / metabolism
  • Pterocarpans / pharmacology*
  • Reactive Oxygen Species / metabolism

Substances

  • Membrane Proteins
  • Neuroprotective Agents
  • Pterocarpans
  • Reactive Oxygen Species
  • Glutamic Acid
  • Heme Oxygenase-1
  • Hmox1 protein, mouse
  • Parp1 protein, mouse
  • Poly (ADP-Ribose) Polymerase-1