Decreased expression of Ras-GRF1 in the brain tissue of the intractable epilepsy patients and experimental rats
Decreased expression of Ras-GRF1 in the brain tissue of the intractable epilepsy patients and experimental rats
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顽固性癫痫患者及实验大鼠脑组织Ras-GRF1表达降低
DOI:
10.1016/j.brainres.2012.11.033
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发表时间:
2013-02
期刊:
影响因子:
--
通讯作者:
Zhu Q, Wang L, Xiao Z, Xiao F, Luo J, Zhang X, Pe
中科院分区:
文献类型:
--
作者:
Zhu Q, Wang L, Xiao Z, Xiao F, Luo J, Zhang X, Pe
Ras-guanine nucleotide-releasing factor 1 (Ras-GRF1) is present mainly at synaptosome and its expression after birth increases in parallel with the development of neuronal circuitry. Evidences suggested that Ras-GRF1 could mediate forms of synaptic plasticity and might participate in the regulation of neuronal excitability and neurite outgrowth though various signal transduction pathway. The aim of this study was to measure Ras-GRF1 expression in brain tissue of patients with drug-refractory temporal lobe epilepsy (TLE) and lithium chloride-pilocarprine kindled rats using double-label immunofluorescence, immunohistochemistry and Western blotting and to discuss the possible role of Ras-GRF1 in TLE. We randomly selected 30 temporal neocortices tissues from patients with TLE and 9 histologically normal temporal neocortices samples from controls. Meanwhile, we investigated the distribution and level of Ras-GRF1 protein expression during the different phases (the acute period, the latent period and the chronic phase) in the epileptic and control rats. Ras-GRF1 was mainly expressed in the plasma membrane and dendrite of neurons, but it was not co-expressed with GFAP-positive astrocytes in the brain tissue of patients and epileptic rats. Compared with controls, Ras-GRF1 expression was significantly decreased in TLE patients. Ras-GRF1 expression in epileptic rats was already reduced at 1 day post-seizures, then gradually decreased during the latent period and reached a minimum level during the chronic phase. These results demonstrated that the decreased expression of Ras-GRF1 could be involved in the pathogenesis of human TLE.
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DOI:
--
发表时间:
1994-04
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
K. Touhara;James Inglese;J. Pitcher;G. Shaw;R. Lefkowitz
通讯作者:
K. Touhara;James Inglese;J. Pitcher;G. Shaw;R. Lefkowitz
影响因子:
3.5
作者:
Darcy, Michael J.;Trouche, Stephanie;Jin, Shan-Xue;Feig, Larry A.
通讯作者:
Feig, Larry A.
DOI:
10.1523/jneurosci.20-13-05024.2000
发表时间:
2000-07
期刊:
The Journal of Neuroscience
影响因子:
--
作者:
Wai T. Wong;B. Faulkner-Jones;J. Sanes;R. Wong
通讯作者:
Wai T. Wong;B. Faulkner-Jones;J. Sanes;R. Wong
影响因子:
3.5
作者:
Jae-Won Yang;Thomas Czech;M. Felizardo;C. Baumgartner;Gert Lubec
通讯作者:
Jae-Won Yang;Thomas Czech;M. Felizardo;C. Baumgartner;Gert Lubec
DOI:
--
发表时间:
1992
期刊:
Epilepsy research. Supplement
影响因子:
--
作者:
Luiz E. Mello;E. Cavalheiro;Tan Am;J. Pretorius;T. Babb;D. Finch
通讯作者:
Luiz E. Mello;E. Cavalheiro;Tan Am;J. Pretorius;T. Babb;D. Finch