Inhibiting SRC activity attenuates kainic-acid induced mouse epilepsy via reducing NR2B phosphorylation and full-length NR2B expression

被引:3
|
作者
Liu, Lu [1 ]
Xia, Lu [1 ]
Li, Yuxiang [1 ]
Zhang, Yiying [1 ]
Wang, Qiang [1 ]
Ding, Jing [1 ]
Wang, Xin [1 ,2 ,3 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Neurol, Fenglin Rd, Shanghai 200032, Peoples R China
[2] Fudan Univ, Inst Brain Sci, Dept State Key Lab Med Neurobiol, Shanghai, Peoples R China
[3] Fudan Univ, Collaborat Innovat Ctr Brain Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Seizure; SRC; NR2B; Neuron loss; Mossy fibre sprouting; D-ASPARTATE RECEPTORS; MEDIATED PHOSPHORYLATION; NMDA; CALPAIN; FYN; EPILEPTOGENESIS; ACCUMULATION; ACTIVATION; SUBUNITS; SURGERY;
D O I
10.1016/j.eplepsyres.2022.106975
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To explore the effect of SRC activation on spontaneously recurrent seizures and to investigate the underlying mechanisms of NR2B phosphorylation. Methods: C57BL/6 mice were injected intrahippocampally with kainic acid (KA, 0.4 mu g/25 g) to induce status epilepticus (SE). Saracatinib(STB) was used as an SRC inhibitor. Spontaneously recurrent seizures were monitored from day 7 to day 14 after the KA injection. Nissl's stain and NeuN were used to detect neuron loss and Timm stain was used to evaluate mossy fibre sprouting 14 days after KA injection. We also investigated the effect of SRC on full-length expression of NR2B. MDL28170 was used to inhibit calpain activity. Western blotting and qPCR were performed to verify phosphorylation levels and expression of SRC and NR2B 24 h after KA injection. Results: The duration of status epileptics in the SRC inhibitor group decreased significantly compared to the KA group 24 h after the injection of KA (P < 0.05). The application of the SRC inhibitor significantly reduced the degree of contralateral mossy fibre sprouting (P < 0.05) and improved the degree of neuron loss (P < 0.01) compared to the epilepsy group. Full-length NR2B levels in the ipsilateral hippocampus decreased in the epilepsy group (P < 0.01) compared to the sham group, and it further decreased in the STB inhibitor group (P < 0.01). The effect of the STB inhibitor was counteracted by simultaneous inhibition of SRC activity and calpain activation, while the level of full-length NR2B increased compared to the KA+STB group(P < 0.01). Reduction of NR2B cleavage by MDL28170 significantly increased the duration of epileptic status compared to the KA group (P < 0.05). Significance: Our data indicated that the early application of SRC inhibitors exerted protective effects on seizure severity, loss of neurons, and sprouting of mossy fibres in KA-induced mouse epilepsy. Seizure severity attenuation due to SRC inhibition was associated with the decrease of NR2B in both the phosphorylation and full-length forms.
引用
收藏
页数:10
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