Binder Devin K, Oshio Kotaro, Ma Tonghui, Verkman A S, Manley Geoffrey T
Department of Neurological Surgery, University of California, 505 Parnassus Ave, Box 0112, San Francisco, CA 94143, USA.
Neuroreport. 2004 Feb 9;15(2):259-62. doi: 10.1097/00001756-200402090-00009.
Mice deficient in the glial water channel aquaporin-4 (AQP4) show decreased cerebral edema and improved neurological outcome following water intoxication or ischemic challenge. In this report, we tested seizure susceptibility in AQP4 mice. AQP4 mice and wild-type controls were given the chemoconvulsant pentylenetetrazol (PTZ) and monitored for seizure activity. At 40 mg/kg PTZ, all wild-type mice exhibited seizure activity, whereas six of seven AQP4 mice did not exhibit seizure activity. At 50 mg/kg PTZ, both groups exhibited seizure activity; however, the latency to generalized (tonic-clonic) seizures was significantly lower in wild-type than AQP4 mice. These results suggest that glial water channels may modulate brain excitability and the initiation and generalization of seizure activity.
缺乏胶质水通道蛋白-4(AQP4)的小鼠在水中毒或缺血刺激后,脑水肿减轻,神经功能预后改善。在本报告中,我们测试了AQP4小鼠的癫痫易感性。给AQP4小鼠和野生型对照注射化学惊厥剂戊四氮(PTZ),并监测癫痫活动。在40mg/kg PTZ时,所有野生型小鼠均出现癫痫活动,而7只AQP4小鼠中有6只未出现癫痫活动。在50mg/kg PTZ时,两组均出现癫痫活动;然而,野生型小鼠全身性(强直阵挛性)癫痫发作的潜伏期明显短于AQP4小鼠。这些结果表明,胶质水通道可能调节大脑兴奋性以及癫痫活动的起始和扩散。