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Effects of Hindlimb Unweighting on MBP and GDNF Expression and Morphology in Rat Dorsal Root Ganglia Neurons
Authors:Zhang  Heng  Ren  Ning-tao  Zhou   Fang-qiang  Li   Jie  Lei   Wei  Liu   Ning  Bi   Long  Wu   Zi-xiang  Zhang   Ran  Zhang   Yong-gang  Cui   Geng
Affiliation:1.Department of Orthopedics, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China
;2.Shanghai Sandai Pharmaceutical R&D Company, Ltd., Shanghai, 201203, China
;3.Institute of Gynaecology and Obstetrics, Chinese PLA General Hospital, Beijing, 100853, China
;4.Department of Orthopaedic Surgery, Xijing Hospital, The Fourth Military Medical University, Xi’an, 710032, China
;5.Department of Cardiology, Chinese PLA General Hospital, Beijing, 100853, China
;
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.

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