A1 Journal article (refereed)
Water-Soluble Cuprizone Derivative: Synthesis, Characterization, and in Vitro Studies (2019)
Fries, M., Mertens, M., Teske, N., Kipp, M., Beyer, C., Willms, T., Valkonen, A., Rissanen, K., Albrecht, M., & Clarner, T. (2019). Water-Soluble Cuprizone Derivative: Synthesis, Characterization, and in Vitro Studies. ACS Omega, 4(1), 1685-1689. https://doi.org/10.1021/acsomega.8b02523
JYU authors or editors
Publication details
All authors or editors: Fries, Martin; Mertens, Meike; Teske, Nico; Kipp, Markus; Beyer, Cordian; Willms, Thomas; Valkonen, Arto; Rissanen, Kari; Albrecht, Markus; Clarner, Tim
Journal or series: ACS Omega
ISSN: 2470-1343
eISSN: 2470-1343
Publication year: 2019
Volume: 4
Issue number: 1
Pages range: 1685-1689
Publisher: American Chemical Society
Publication country: United States
Publication language: English
DOI: https://doi.org/10.1021/acsomega.8b02523
Publication open access: Openly available
Publication channel open access: Open Access channel
Publication is parallel published (JYX): https://jyx.jyu.fi/handle/123456789/62592
Abstract
The cuprizone mouse model is one of the most accepted model systems for the investigation of oligodendrocyte degeneration, a process critically involved in the pathogenesis of diseases such as multiple sclerosis or schizophrenia. In order to substitute the in vivo experiments by in vitro approaches, the amine derivative BiMPi is introduced as a water-soluble alternative to cuprizone. Regarding superoxide dismutase activity, toxicity for oligodendrocytes, and disturbance of mitochondrial membrane potential, BiMPi shows similar in vitro effects as is observed in vivo for cuprizone.
Keywords: neurochemistry; pathogenesis; amines; chemical synthesis; in vitro method; synthesis
Free keywords: water-soluble cuprizone derivative; characterization; in Vitro studies
Contributing organizations
Related projects
- Robust S...I+...S Halogen Bonded Supramolecular Assemblies (research costs)
- Valkonen, Arto
- Research Council of Finland
Ministry reporting: Yes
VIRTA submission year: 2019
JUFO rating: 1