Garcimartin_2017_Redox.Biol_12_719

Reference

Title : Hydrogen peroxide modifies both activity and isoforms of acetylcholinesterase in human neuroblastoma SH-SY5Y cells - Garcimartin_2017_Redox.Biol_12_719
Author(s) : Garcimartin A , Lopez-Oliva ME , Gonzalez MP , Sanchez-Muniz FJ , Benedi J
Ref : Redox Biol , 12 :719 , 2017
Abstract :

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 (1-1000microM) for 24h and AChE activity and AChE and cytochrome c levels were evaluated. AChE activity was strongly increased from 1microM to 1000microM 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, (100-1000microM) reduced the total AChE content and modified its isoform profile (mainly 50-, 70-, and 132-kDa).H2O2 from 100microM to 1000microM 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.

PubMedSearch : Garcimartin_2017_Redox.Biol_12_719
PubMedID: 28411556

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Citations formats

Garcimartin A, Lopez-Oliva ME, Gonzalez MP, Sanchez-Muniz FJ, Benedi J (2017)
Hydrogen peroxide modifies both activity and isoforms of acetylcholinesterase in human neuroblastoma SH-SY5Y cells
Redox Biol 12 :719

Garcimartin A, Lopez-Oliva ME, Gonzalez MP, Sanchez-Muniz FJ, Benedi J (2017)
Redox Biol 12 :719