The Cuprizone Mouse Model: A Comparative Study of Cuprizone Formulations from Different Manufacturers

被引:7
作者
Beecken, Malena [1 ]
Baumann, Louise [1 ]
Vankriekelsvenne, Elise [1 ]
Manzhula, Katerina [1 ]
Greiner, Theresa [1 ]
Heinig, Leo [1 ]
Schauerte, Steffen [2 ]
Kipp, Markus [1 ]
Joost, Sarah [1 ]
机构
[1] Rostock Univ, Inst Anat, Med Ctr, D-18057 Rostock, Germany
[2] Rhein Westfal TH Aachen, Inst Organ Chem, D-52074 Aachen, Germany
关键词
Cuprizone mouse model; demyelination; astrogliosis; microgliosis; INDUCED DEMYELINATION; STRAIN;
D O I
10.3390/ijms241310564
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Cuprizone mouse model is widely used in studies on de- and remyelination. In the hands of different experimenters, the Cuprizone concentrations that lead to comparable levels of demyelination differ considerably. The reasons for this variability are unknown. In this study, we tested whether different Cuprizone formulations from different vendors and manufacturers influenced Cuprizone-induced histopathological hallmarks. We intoxicated male C57BL/6 mice with six Cuprizone powders that differed in their manufacturer, vendor, and purity. After five weeks, we analyzed the body weight changes over the course of the experiment, as well as the demyelination, astrogliosis, microgliosis and axonal damage by histological LFB-PAS staining and immunohistochemical labelling of PLP, IBA1, GFAP and APP. All Cuprizone formulations induced demyelination, astrogliosis, microgliosis, axonal damage and a moderate drop in body weight at the beginning of the intoxication period. In a cumulative evaluation of all analyses, two Cuprizone formulations performed weaker than the other formulations. In conclusion, all tested formulations did work, but the choice of Cuprizone formulation may have been responsible for the considerable variability in the experimental outcomes.
引用
收藏
页数:16
相关论文
共 32 条
[1]   Distribution of oligodendrocyte loss and mitochondrial toxicity in the cuprizone-induced experimental demyelination model [J].
Acs, P. ;
Selak, M. A. ;
Komoly, S. ;
Kalman, B. .
JOURNAL OF NEUROIMMUNOLOGY, 2013, 262 (1-2) :128-131
[2]  
CARLTON WILLIAM W., 1967, LIFE SCI, V6, P11, DOI 10.1016/0024-3205(67)90356-6
[3]  
Filippi M, 2018, NAT REV DIS PRIMERS, V4, DOI [10.1038/s41572-018-0041-4, 10.1038/s41572-018-0046-z]
[4]   Delayed Demyelination and Impaired Remyelination in Aged Mice in the Cuprizone Model [J].
Gingele, Stefan ;
Henkel, Florian ;
Heckers, Sandra ;
Moellenkamp, Thiemo M. ;
Huemmert, Martin W. ;
Skripuletz, Thomas ;
Stangel, Martin ;
Gudi, Viktoria .
CELLS, 2020, 9 (04)
[5]   Anatomical Distribution of Cuprizone-Induced Lesions in C57BL6 Mice [J].
Goldberg, Johannes ;
Clarner, Tim ;
Beyer, Cordian ;
Kipp, Markus .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2015, 57 (02) :166-175
[6]   Glial response during cuprizone-induced de- and remyelination in the CNS: lessons learned [J].
Gudi, Viktoria ;
Gingele, Stefan ;
Skripuletz, Thomas ;
Stangel, Martin .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2014, 8
[7]   Abnormal oxidative metabolism in the cuprizone mouse model of demyelination: An in vivo NIRS-MRI study [J].
Hashem, Mada ;
Shafqat, Qandeel ;
Wu, Ying ;
Rho, Jong M. ;
Dunn, Jeff F. .
NEUROIMAGE, 2022, 250
[8]   In toxic demyelination oligodendroglial cell death occurs early and is FAS independent [J].
Hesse, Amke ;
Wagner, Michael ;
Held, Jasmin ;
Brikk, Wolfgang ;
Salinas-Riester, Gabriela ;
Hao, Zhenyue ;
Waisman, Ari ;
Kuhlmann, Tanja .
NEUROBIOLOGY OF DISEASE, 2010, 37 (02) :362-369
[9]   Microglial/macrophage accumulation during cuprizone-induced demyelination in C57BL/6 mice [J].
Hiremath, MM ;
Saito, Y ;
Knapp, GW ;
Ting, JPY ;
Suzuki, K ;
Matsushima, GK .
JOURNAL OF NEUROIMMUNOLOGY, 1998, 92 (1-2) :38-49
[10]   Cuprizone-Containing Pellets Are Less Potent to Induce Consistent Demyelination in the Corpus Callosum of C57BL/6 Mice [J].
Hochstrasser, Tanja ;
Exner, Gianna Lisa ;
Nyamoya, Stella ;
Schmitz, Christoph ;
Kipp, Markus .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2017, 61 (04) :617-624