| Literature DB >> 27377070 |
Nabil El Massri1, Cécile Moro2, Napoleon Torres2, Fannie Darlot2, Diane Agay2, Claude Chabrol2, Daniel M Johnstone3, Jonathan Stone3, Alim-Louis Benabid2, John Mitrofanis4.
Abstract
We have reported previously that intracranial application of near-infrared light (NIr) reduces clinical signs and offers neuroprotection in a subacute MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) monkey model of Parkinson's disease. In this study, we explored whether NIr reduces the gliosis in this animal model. Sections of midbrain (containing the substantia nigra pars compacta; SNc) and striatum were processed for glial fibrillary acidic protein (to label astrocytes; GFAP) and ionised calcium-binding adaptor molecule 1 (to label microglia; IBA1) immunohistochemistry. Cell counts were undertaken using stereology, and cell body sizes were measured using ImageJ. Our results showed that NIr treatment reduced dramatically (~75 %) MPTP-induced astrogliosis in both the SNc and striatum. Among microglia, however, NIr had a more limited impact in both nuclei; although there was a reduction in overall cell size, there were no changes in the number of microglia in the MPTP-treated monkeys after NIr treatment. In summary, we showed that NIr treatment influenced the glial response, particularly that of the astrocytes, in our monkey MPTP model of Parkinson's disease. Our findings raise the possibility of glial cells as a future therapeutic target using NIr.Entities:
Keywords: 670 nm; Parkinson’s disease; Photobiomodulation; Striatum; Substantia nigra
Mesh:
Substances:
Year: 2016 PMID: 27377070 DOI: 10.1007/s00221-016-4720-7
Source DB: PubMed Journal: Exp Brain Res ISSN: 0014-4819 Impact factor: 2.064