Endogenous hydrogen sulfide is involved in asymmetric dimethylarginine-induced protection against neurotoxicity of 1-methyl-4-phenyl-pyridinium ion

Neurochem Res. 2011 Nov;36(11):2176-85. doi: 10.1007/s11064-011-0542-y. Epub 2011 Jul 7.

Abstract

Asymmetric dimethylarginine (ADMA), an endogenous nitric oxide synthase (NOS) inhibitor, is profoundly protective against 1-methy-4-phenylpyridinium ion (MPP+)-induced neurotoxicity. Reactive oxygen species (ROS) overproduction contributes to the neurotoxicity of MPP+; while hydrogen sulfide (H₂S) is a pivotal endogenous antioxidant. This study is to assess the potential role of endogenous H₂S in the neuroprotection of ADMA against MPP+-induced toxicity in PC12 cells. We showed that ADMA prevented MPP+-induced inhibition of endogenous H₂S generation through inhibiting the down-regulation of cystathionine-β-synthetase (CBS, the major enzyme responsible for endogenous H₂S generation in PC12 cells) expression and activity elicited by MPP+. ADMA obviously attenuated MPP+-triggered accumulation of intracellular ROS, dissipation of mitochondrial membrane potential (MMP), release of cytochrome c (Cyt-c), and downregulation of Bcl-2 protein expression in PC12 cells. Inhibition of CBS activity by amino-oxyacetate and CBS silencing with a short hairpin RNA vector targeting rat CBS gene reversed the protective action of ADMA against MPP+-caused cytotoxicity, ROS overproduction, and MMP loss in PC12 cells. These results indicate that the protection of ADMA against MPP+-mediated neurotoxicity involves the melioration of MPP+-induced inhibition of endogenous H₂S generation. Our findings suggest that modulation of H₂S production provide new therapeutic targets for the treatment of neurodegenerative disease, such as Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenylpyridinium / pharmacology
  • 1-Methyl-4-phenylpyridinium / toxicity*
  • Aminooxyacetic Acid / pharmacology
  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology
  • Arginine / analogs & derivatives*
  • Arginine / pharmacology
  • Cyclin D1 / biosynthesis
  • Cystathionine beta-Synthase / antagonists & inhibitors
  • Cystathionine beta-Synthase / biosynthesis
  • Cytochromes c / metabolism
  • Down-Regulation / drug effects
  • Hydrogen Sulfide / metabolism*
  • Hydrogen Sulfide / pharmacology
  • Membrane Potential, Mitochondrial / drug effects
  • Neuroprotective Agents / pharmacology*
  • PC12 Cells
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • Antioxidants
  • Neuroprotective Agents
  • Reactive Oxygen Species
  • Cyclin D1
  • Aminooxyacetic Acid
  • N,N-dimethylarginine
  • Cytochromes c
  • Arginine
  • Cystathionine beta-Synthase
  • 1-Methyl-4-phenylpyridinium
  • Hydrogen Sulfide