4.7 Article

Hydrogen peroxide modifies both activity and isoforms of acetylcholinesterase in human neuroblastoma SH-SY5Y cells

Journal

REDOX BIOLOGY
Volume 12, Issue -, Pages 719-726

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.redox.2017.04.004

Keywords

Acetylcholinesterase; Hydrogen peroxide; Alternative splicing; Cell culture; Cell death

Funding

  1. Spanish Projects [AGL2011-29644-C02-02, AGL2014-53207-C2-2-R]
  2. Spanish Ministry of Economy and Competitiveness [BES-2012-054752 (FPI)]

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The involvement of cholinergic system and the reactive oxygen species (ROS) in the pathogenesis of some degenerative diseases has been widely reported; however, the specific impact of hydrogen peroxide (H2O2) on the acetylcholinesterase (AChE) activity as well as AChE isoform levels has not been clearly established. Hence, the purpose of present study is to clarify whether H2O2 alters these parameters. Human neuroblastoma SH- SY5Y cells were treated with H2O2 (1-1000 mu M) for 24 h and AChE activity and AChE and cytochrome c levels were evaluated. AChE activity was strongly increased from 1 mu M to 1000 mu M of H2O2. The results of the kinetic study showed that H2O2 affected Vmax but not Km; and also that H2O2 changed the sigmoid kinetic observed in control samples to hyperbolic kinetic. Thus, results suggest that H2O2 acts as an allosteric activators. In addition, H2O2, (100-1000 mu M) reduced the total AChE content and modified its isoform profile (mainly 50-, 70-, and 132-kDa) center dot H2O2 from 100 mu M to 1000 mu M induced cytochrome c release confirming cell death by apoptosis. All these results together suggest: a) the involvement of oxidative stress in the imbalance of AChE; and b) treatment with antioxidant agents may be a suitable strategy to protect cholinergic system alterations promoted by oxidative stress.

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