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Acrolein: An Effective Biomarker for Tissue Damage Produced from Polyamines
Kazuei Igarashi1,2, Takeshi Uemura3, Keiko Kashiwagi4
1Amine Pharma Research Institute, Innovation Plaza at Chiba University, 1-8-15 Inohana, Chuo-ku, Chiba, 260-0856, Japan. iga16077@faculty.chiba-u.jp.
Methods in Molecular Biology (Clifton, N.J.)
|October 29, 2017
Summary
Acrolein, a toxic compound produced from spermine and spermidine, is more damaging than reactive oxygen species (ROS). This chapter details acrolein
Area of Science:
- Biochemistry
- Neuroscience
- Toxicology
Background:
- Reactive oxygen species (ROS) are traditionally considered the primary cause of cell damage.
- Recent studies indicate that acrolein, a compound derived from spermine and spermidine, exhibits greater toxicity than ROS.
Purpose of the Study:
- To elucidate the mechanism of acrolein production during brain stroke.
- To describe a mechanism underlying acrolein's toxicity.
- To investigate the role of glutathione in detoxifying acrolein.
Main Methods:
- Mechanistic studies on acrolein formation pathways.
- Investigation of cellular responses to acrolein exposure.
- Biochemical assays to assess glutathione's role in detoxification.
Main Results:
- Identified acrolein as a significant toxic agent in brain stroke, surpassing ROS.
- Elucidated a specific pathway through which acrolein induces cellular damage.
- Demonstrated the protective effect of glutathione against acrolein toxicity.
Conclusions:
- Acrolein is a critical mediator of cell damage in brain stroke.
- Understanding acrolein's toxicity mechanisms is crucial for therapeutic interventions.
- Glutathione plays a vital role in mitigating acrolein-induced cellular injury.
Keywords:
AcroleinBrain infarctionGAPDH (glyceraldehyde-3-phosphate dehydrogenase)GSH (glutathione)SpermineSpermine oxidase
