Analysis of platelet-derived growth factor receptor A and oligodendrocyte transcription factor 2 markers following Hydroxychloroquine administration in animal induced multiple sclerosis model

(2021) Analysis of platelet-derived growth factor receptor A and oligodendrocyte transcription factor 2 markers following Hydroxychloroquine administration in animal induced multiple sclerosis model. METABOLIC BRAIN DISEASE. pp. 2101-2110. ISSN 0885-7490 1573-7365 J9 - METAB BRAIN DIS

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Abstract

It has been shown that following demyelination, Oligodendrocyte Progenitor Cells (OPCs) migrate to the lesion site and begin to proliferate, and differentiate. This study aimed to investigate the effects of Hydroxychloroquine (HCQ) on the expression of OLIG-2 and PDGFR-alpha markers during the myelination process. C57BL/6 mice were fed cuprizone pellets for 5 weeks to induce demyelination and return to a normal diet for 1 week to stimulate remyelination. During the Phase I all of the animals except CPZ and Vehicle groups were exposed to HCQ (2.5, 10, and 100 mg/kg) via drinking water. At the end of the study, animals were euthanized, perfused and the brain samples were assessed for myelination and immunohistochemistry evaluation. What is remarkable is the high rate of Olig2 + cells in the groups treated with 10 and 100 mg/kg HCQ in the demyelination phase and its decreasing trend in the remyelination phase. However, there was no significant difference between groups during phase I and Phase II based on the percentage of olig-2+/total cells in the corpus callosum region. The number of PDGFR-alpha+ cells in the group treated with 10 mg/kg HCQ was significant in the first phase (p value < 0.05). Considering that the 100 mg/kg HCQ group had the highest level of PDGFR-alpha as well as the highest level of myelin repair in LFB staining, it could be inferred that it was the most effective dose in inducing proliferation and migration of OPCs.

Item Type: Article
Keywords: Cuprizone Hydroxychloroquine PDGFR-alpha Olig-2 OPC Myelin Immunohistochemistry PROGENITOR CELLS TENASCIN-C REMYELINATION PROLIFERATION CNS DIFFERENTIATION REPAIR DECREASE LESIONS OLIG1
Page Range: pp. 2101-2110
Journal or Publication Title: METABOLIC BRAIN DISEASE
Journal Index: ISI
Volume: 36
Number: 7
Identification Number: https://doi.org/10.1007/s11011-021-00802-8
ISSN: 0885-7490 1573-7365 J9 - METAB BRAIN DIS
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/17381

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