| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2203509 | Tissue and Cell | 2016 | 10 Pages |
•Demyelination of corpus callosum was induced by two weeks of cuprizone ingestion.•T3 increased expression of MBP and PLP gene and myelinated axons compared to saline.•T3 directs progenitors toward oligodendrocytes maturation.•This was especially evident after three weeks of cuprizone withdrawal.
Demyelination was induced by two weeks cuprizone treatment. Rats of +ve control and triiodothyronine (T3) then received three subcutaneous injections of either saline or T3 day after day and sacrificed at the end of the third and fifth weeks. Animals in −ve control group received only standard rodent chow. After one week of cuprizone withdrawal the corpus callosum in +ve control and T3 treated rats was still demyelinated as revealed by MBP immunohistochemistry. The assay of PLP gene showed significant increase of T3 treated group compared to both the −ve control and +ve control groups. After three weeks, significant improvement in myelination was detected in T3-treated group compared to +ve control as detected by both MBP immunohistochemistry and electron microscopy. After one week of cuprizone withdrawal, PDGFRα positive cells and gene expression showed significant increase in +ve control and T3-treated groups as compared to −ve control with insignificant difference in between the former two groups. After three weeks of cuprizone withdrawal, PDGFRα positive cells in T3-treated and +ve control groups decreased to the control levels. These results suggest that T3 was effective in improving remyelination when administered during acute phase and might direct progenitor lineage toward oligodendrocytes.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (217 K)Download as PowerPoint slide
