The effect of behavioral training on neural stem cell differentiation in the dentate gyrus of rats with hippocampal infarction
10.3760/cma.j.issn.0254-1424.2009.04.002
- VernacularTitle:行为学训练对海马梗死大鼠齿状回区神经干细胞分化能力的影响
- Author:
Yana LI
;
Ling LI
;
Hua YUAN
;
Xiang MU
;
Shan JIANG
- Publication Type:Journal Article
- Keywords:
Rats;
Dentate gyrus;
BrdU;
NeuN;
GFAP;
Neural stem cell;
Differentiation
- From:
Chinese Journal of Physical Medicine and Rehabilitation
2009;31(4):219-223
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effect of behavioral training on the differentiation of neural stem cells in the dental gyrus (DG) in rats with hippocampus infarction. Methods Seventy-eight Sprague-Dawley rats were randomized into infarction plus behavior training group, infarction group and control group. Photochemistry method was used to induce hippocampal infarction in rats of the infarction plus behavioral training group and infarc-tion group. At 1 day after surgery, Morris water maze training was used for infarction plus behavioral training group, free-movement without training was performed for infarction group. Double staining immunofluorescence was used to detect the co-expression of bromodeoxyuridine (BrdU) with neuronal nuclei ( NeuN ) or glia fibrillary acidic protein (GFAP) in the DG at different time points. Results Few BrdU/NeuN and BrdU/GFAP double staining cells were observed in the DG of control rats. In the infarction group and infarction plus behavioral training group the number of BrdU/NeuN and BrdU/GFAP double-stained cells increased in the DG on the opposite side compared with the control group on 14th, 21st, 28th and 35th days after surgery (P < 0.05 ). There observed significantly more BrdU/NeuN and BrdU/GFAP double-stained cells in the infarction plus behavioral training group than that in the infarction group on the 14th, 21st, 28th and 35th days after surgery ( P < 0.05 ). Conclusion Behavioral training can accelerate the differentiation of neural stem cells to neuron and astrocyte, by which to promote the re-covery of neural functions.
