Bo Tao, Chen Yong, Mao Ding-An, Zhu Xiao-Hua, Li Yan-Fang
Department of Pediatrics, Second Xiangya Hospital, Central Southern Universality, Changsha 410011, China.
Zhonghua Yi Xue Za Zhi. 2007 Jan 23;87(4):275-8.
To investigate the long-term effects of recurrent seizures in neonate period on the expression of gamma-aminobutyric acid A receptor (GABAAR) alpha1 and beta2 subunits in brain and spatial memory and seizure susceptibility in adult period.
Thirty-two 7-day-old SD rats were randomly divided into 2 equal groups: seizure group, inhaling flurothyl to induce seizure daily for 6 days, and control group. On days 61 - 65 after birth Morris water maze test was used to record the escape latency. On day 75 after birth pentylenetetrazol (PTZ) was injected intraperitoneally to induce seizure so as to record the latency. Then the rats were killed to take their brains, 8 in each group used to undergo immunohistochemistry to examine the protein expression of the GABAAR alpha1 and beta2 subunits, and the other 8 in each group used to examine the mRNA expression of the GABAAR alpha1 and beta2 subunits in the brains using RT-PCR.
On day 64 the escape latency of the seizure group was 82,424 ms +/- 35,622 ms, significantly longer than that of the control group (40,712 ms +/- 29,468 ms, P = 0.001). On day 75 the frequency of crossing target within 120 s in the water maze of the seizure group was 1.2 times +/- 0.9 times, significantly less than that of the control group (3.1 times +/- 1.3 times, P < 0.01). The seizure latency after the PTZ injection of the seizure group was (1487 +/- 662) s, not significantly different from that of the control group (1841 s +/- 648 s, P = 0.133). In comparison with the control group the accumulated optical density (AOD) of GABAAR alpha1 subunit protein immunoactivity in the parietal cortex, and hippocampal CA1-2 and CA4 regions of the seizure group decreased significantly (all P < 0.05), and was not significantly different in the frontal cortex, dentate gyrus, and hippocampal CA3 region (all P > 0.05). In comparison with the control group the accumulated optical density (AOD) of GABAAR beta2 subunit protein immunoactivity in the thalamus, and hippocampal CA1-4 regions of the seizure group decreased significantly (all P < 0.05), and was not significantly different in the frontal cortex and parietal cortex (both P > 0.05). In comparison with the control group the mRNA expression of GABAAR alpha1 subunit and the mRNA expression of GABAAR beta2 subunit of the seizure group were significantly lower in the hippocampus (both P < 0.05) and not significantly different in the cerebral cortex (both P > 0.05).
Recurrent seizures in neonate period modify the expression of GABAAR alpha1 and beta2 subunits in the cerebral cortex and hippocampus in adult period which may be related to cognitive deficit.
探讨新生儿期反复惊厥对成年期大脑中γ-氨基丁酸A受体(GABAAR)α1和β2亚基表达、空间记忆及惊厥易感性的长期影响。
将32只7日龄SD大鼠随机分为2组,每组16只:惊厥组,每日吸入三氟乙烷诱导惊厥,共6天;对照组。出生后61 - 65天,采用Morris水迷宫试验记录逃避潜伏期。出生后75天,腹腔注射戊四氮(PTZ)诱导惊厥,记录惊厥潜伏期。然后处死大鼠取脑,每组8只用于免疫组织化学检测GABAARα1和β2亚基的蛋白表达,每组另外8只用于采用逆转录聚合酶链反应(RT-PCR)检测大脑中GABAARα1和β2亚基的mRNA表达。
在第64天,惊厥组的逃避潜伏期为82424 ms±35622 ms,显著长于对照组(40712 ms±29468 ms,P = 0.001)。在第75天,惊厥组在水迷宫中120 s内穿越目标的次数为1.2次±0.9次,显著少于对照组(3.1次±1.3次,P < 0.01)。惊厥组注射PTZ后的惊厥潜伏期为(1487±662)s,与对照组(1841 s±648 s,P = 0.133)无显著差异。与对照组相比,惊厥组顶叶皮质、海马CA1 - 2区和CA4区GABAARα1亚基蛋白免疫活性的累积光密度(AOD)显著降低(均P < 0.05),在额叶皮质、齿状回和海马CA3区无显著差异(均P > 0.05)。与对照组相比,惊厥组丘脑和海马CA1 - 4区GABAARβ2亚基蛋白免疫活性的累积光密度(AOD)显著降低(均P < 0.05),在额叶皮质和顶叶皮质无显著差异(均P > 0.05)。与对照组相比,惊厥组海马中GABAARα1亚基的mRNA表达和GABAARβ2亚基的mRNA表达显著降低(均P < 0.05),在大脑皮质中无显著差异(均P > 0.05)。
新生儿期反复惊厥可改变成年期大脑皮质和海马中GABAARα1和β2亚基的表达,这可能与认知缺陷有关。