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Epileptogenic effects of NMDAR antibodies in a passive transfer mouse model

机译:NMDAR抗体在被动转移小鼠模型中的致痫作用

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摘要

Most patients with N-methyl D-aspartate-receptor antibody encephalitis develop seizures but the epileptogenicity of the antibodies has not been investigated in vivo. Wireless electroencephalogram transmitters were implanted into 23 C57BL/6 mice before left lateral ventricle injection of antibody-positive (test) or healthy (control) immunoglobulin G. Mice were challenged 48 h later with a subthreshold dose (40 mg/kg) of the chemo-convulsant pentylenetetrazol and events recorded over 1 h. Seizures were assessed by video observation of each animal and the electroencephalogram by an automated seizure detection programme. No spontaneous seizures were seen with the antibody injections. However, after the pro-convulsant, the test mice (n = 9) had increased numbers of observed convulsive seizures (P = 0.004), a higher total seizure score (P = 0.003), and a higher number of epileptic ‘spike’ events (P = 0.023) than the control mice (n = 6). At post-mortem, surprisingly, the total number of N-methyl D-aspartate receptors did not differ between test and control mice, but in test mice the levels of immunoglobulin G bound to the left hippocampus were higher (P < 0.0001) and the level of bound immunoglobulin G correlated with the seizure scores (R2 = 0.8, P = 0.04, n = 5). Our findings demonstrate the epileptogenicity of N-methyl D-aspartate receptor antibodies in vivo, and suggest that binding of immunoglobulin G either reduced synaptic localization of N-methyl D-aspartate receptors, or had a direct effect on receptor function, which could be responsible for seizure susceptibility in this acute short-term model.
机译:患有N-甲基D-天冬氨酸受体抗体脑炎的大多数患者会发作,但尚未在体内研究过抗体的癫痫原性。无线脑电图发射器被植入23只C57BL / 6小鼠中,然后在左心室注射抗体阳性(测试)或健康(对照)免疫球蛋白G。48小时后,以低于阈值剂量(40 mg / kg)的化学疗法攻击小鼠-惊厥性戊四唑,记录事件超过1小时。通过视频观察每只动物评估癫痫发作,并通过自动癫痫发作检测程序对脑电图进行评估。抗体注射未见自发性癫痫发作。然而,在前惊厥后,受试小鼠(n = 9)的观察到的惊厥性癫痫发作次数增加(P = 0.004),总癫痫发作分数更高(P = 0.003)和癫痫发作的次数增多(P = 0.023)比对照组(n = 6)。令人惊讶的是,在死后,测试小鼠和对照组小鼠的N-甲基D-天门冬氨酸受体总数没有差异,但是在测试小鼠中,与左海马结合的免疫球蛋白G水平更高(P <0.0001),并且结合的免疫球蛋白G的水平与癫痫发作评分相关(R 2 = 0.8,P = 0.04,n = 5)。我们的发现证明了体内N-甲基D-天冬氨酸受体抗体的癫痫发生性,并表明免疫球蛋白G的结合可降低N-甲基D-天冬氨酸受体的突触定位,或对受体功能具有直接影响,这可能是造成这种情况的原因。在这种急性短期模型中的癫痫发作易感性。

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