| Literature DB >> 27230884 |
Heng Zhang1, Ning-Tao Ren1, Fang-Qiang Zhou2, Jie Li3, Wei Lei4, Ning Liu4, Long Bi4, Zi-Xiang Wu4, Ran Zhang5, Yong-Gang Zhang1, Geng Cui6.
Abstract
With the development of technology and space exploration, studies on long-duration space flights have shown that microgravity induces damage to multiple organs, including the dorsal root ganglia (DRG). However, very little is known about the effects of long-term microgravity on DRG neurons. This study investigated the effects of microgravity on lumbar 5 (L5) DRG neurons in rats using the hindlimb unweighting (HU) model. Male (M) and female (F) Sprague-Dawley rats were randomly divided into M- and F-control (CON) groups and M- and F-HU groups, respectively (n = 10). At the end of HU treatment for 4 weeks, morphological changes were detected. Myelin basic protein (MBP) and degenerated myelin basic protein (dgen-MBP) expressions were analyzed by immunofluorescence and western blot assays. Glial cell line-derived neurotrophic factor (GDNF) protein and mRNA expressions were also analyzed by immunohistochemistry, western blot, and RT-PCR analysis, respectively. Compared with the corresponding CON groups, the HU groups exhibited slightly loose junctions between DRG neurons, some separated ganglion cells and satellite cells, and lightly stained Nissl bodies that were of smaller size and had a scattered distribution. High levels of dgen-MBP and low MBP expressions were appeared and GDNF expressions were significantly decreased in both HU groups. Changes were more pronounced in the F-HU group than in the M-HU group. In conclusion, HU treatment induced damage of L5 DRG neurons, which was correlated with decreased total MBP protein expression, increased dgen-MBP expression, and reduced GDNF protein and mRNA expression. Importantly, these changes were more severe in F-HU rats compared with M-HU rats.Entities:
Keywords: Dorsal root ganglia; Glial cell line-derived neurotrophic factor; Hindlimb unweighting; Myelin basic protein; Neuron
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Year: 2016 PMID: 27230884 DOI: 10.1007/s11064-016-1956-3
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996