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Bone marrow-derived mesenchymal stem cells increase dopamine synthesis in the injured striatum 被引量:3
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作者 Yue Huang Cheng Chang +1 位作者 Jiewen Zhang xiaoqun gao 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第34期2653-2662,共10页
Previous studies showed that tyrosine hydroxylase or neurturin gene-modified cells transplanted into rats with Parkinson's disease significantly improved behavior and increased striatal dopamine content. In the prese... Previous studies showed that tyrosine hydroxylase or neurturin gene-modified cells transplanted into rats with Parkinson's disease significantly improved behavior and increased striatal dopamine content. In the present study, we transplanted tyrosine hydroxylase and neurturin gene-modified bone marrow-derived mesenchymal stem cells into the damaged striatum of Parkinson's disease model rats. Several weeks after cell transplantation, in addition to an improvement of motor function tyrosine hydroxylase and neurturin proteins were up-regulated in the injured striatum, and importantly, levels of dopamine and its metabolite 3,4-dihydroxyphenylacetic acid increased significantly. Furthermore, the density of the D2 dopamine receptor in the postsynaptic membranes of dopaminergic neurons was decreased. These results indicate that transplantation of tyrosine hydroxylase and neurturin gene-modified bone marrow-derived mesenchymal stem cells increases dopamine synthesis and significantly improves the behavior of rats with Parkinson's disease. 展开更多
关键词 Parkinson's disease tyrosine hydroxylase NEURTURIN bone marrow-derived mesenchymal stemcells transplantation dopamine gene therapy neurodegenerative disease regeneration neural
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Ceramide is involved in alcohol-induced neural proliferation 被引量:1
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作者 Zhixin Wang Tongxing Deng +6 位作者 Jiexin Deng Jinbo Deng xiaoqun gao Yuanyuan Shi Bin Liu Zhanyou Ma Haixiao Jin 《Neural Regeneration Research》 SCIE CAS CSCD 2013年第23期2178-2189,共12页
Prenatal alcohol exposure, especially during early pregnancy, can lead to fetal alcohol syndrome. The pharmacological and toxicological mechanisms of ethanol are related to the effects of ceramide In this study, we es... Prenatal alcohol exposure, especially during early pregnancy, can lead to fetal alcohol syndrome. The pharmacological and toxicological mechanisms of ethanol are related to the effects of ceramide In this study, we established an alcohol exposure model in wild-type mice and in knockout mice for the key enzyme involved in ceramide metabolism, sphingomyelin synthase 2. This model received daily intragastric administration of 25% ethanol, and pups were used at postnatal days 0, 7, 14, 30 for experiments. Serology and immunofluorescence staining found that ethanol exposure dose-dependently reduced blood sphingomyelin levels in two genotypes of pups, and increased neural cell proliferation and the number of new neurons in the hippocampal dentate gyrus. Western blot analysis showed that the relative expression level of protein kinase C e increased in two genotypes of pups after ethanol exposure. Compared with witd-type pups, the expression level of the important activator protein of the ceramide/ceramide-l-phosphate pathway, protein kinase C a, was reduced in the hippocampus of sphingomyelin synthase 2 knockouts. Our findings illustrate that ceramide is involved in alcohol-induced neural proliferation in the hippocampal dentate gyrus of pups after prenatal ethanol exposure, and the mechanism may be associated with increased ex- pression of protein kinase C a activating the ceramide/ceramide-l-phosphate pathway. 展开更多
关键词 neural regeneration brain injury CERAMIDE neural cells PROLIFERATION prenatal alcohol exposure sphingomyelin synthase 2 knockout mice SPHINGOMYELIN sphingomyelin synthase cera-mide-l-phosphate fetal alcohol syndrome grants-supported paper NEUROREGENERATION
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