SIN-1 cytotoxicity to PC12 cells is mediated by thiol-sensitive short-lived substances generated through SIN-1 decomposition in culture medium

Nitric Oxide. 2009 Jun;20(4):270-8. doi: 10.1016/j.niox.2009.02.001. Epub 2009 Feb 20.

Abstract

As a generator of peroxynitrite (ONOO(-)), 3-morpholinosydnonimine (SIN-1) is widely used in the study of oxidative/nitrosative stress in cultured cells, although controversy exists regarding active species responsible for cytotoxicity. In this study, we report that unstable thiol-sensitive substances, generated from the reaction of SIN-1 with components in culture medium, play a crucial role in SIN-1 cytotoxicity in PC12 cells. Exposure of cells to culture medium obtained after almost complete SIN-1 decomposition at 37 degrees C for 2h demonstrated almost the same degree of cytotoxicity as did fresh SIN-1. The cytotoxicity of SIN-1-decomposed medium largely depended on serum, decayed with time, and could be completely abolished by the addition of thiols. Degradation of synthetic ONOO(-) in the culture medium did not reproduce the unstable cytotoxicity. The presence of superoxide dismutase (SOD) during SIN-1 decomposition prevented the formation of the cytotoxic substances, whereas SOD had no protection against the cytotoxicity itself, suggesting a crucial role of simultaneously generated superoxide and nitric oxide in the formation of the toxicants, but not in their cytotoxic action. The cytotoxicity of fresh SIN-1 is dramatically suppressed in a basal medium (Hanks balanced salt), suggesting that the cytotoxicity of fresh SIN-1 also requires components of culture medium. These results suggest that SIN-1 cytotoxicity in PC12 cells is mediated via the generation of cytotoxic substances in the medium during its decomposition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caspase 3 / metabolism
  • Cell Death
  • Cells, Cultured
  • Enzyme Inhibitors / toxicity*
  • Molsidomine / analogs & derivatives*
  • Molsidomine / toxicity
  • Oxidative Stress
  • PC12 Cells
  • Peroxynitrous Acid / metabolism
  • Rats
  • Sulfhydryl Compounds / metabolism*
  • Superoxide Dismutase / antagonists & inhibitors
  • Superoxide Dismutase / metabolism

Substances

  • Enzyme Inhibitors
  • Sulfhydryl Compounds
  • Peroxynitrous Acid
  • linsidomine
  • Molsidomine
  • Superoxide Dismutase
  • Caspase 3