中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2010年
5期
437-440
,共4页
邸伟%易咏红%曾志涌%徐明明%王玉良%孙卫文%廖卫平
邸偉%易詠紅%曾誌湧%徐明明%王玉良%孫衛文%廖衛平
저위%역영홍%증지용%서명명%왕옥량%손위문%료위평
脆性X综合征%癫痫%中间神经元%微白蛋白
脆性X綜閤徵%癲癇%中間神經元%微白蛋白
취성X종합정%전간%중간신경원%미백단백
Fragile X syndrome%Epilepsy%Interneurons%Parvalbumin
目的 探讨微白蛋白(PV)阳性中间神经元在脆性X综合征(FXS)癫痫易感性增加中的作用. 方法 应用免疫组织化学染色检测FVB近交系雄性2、4、6 W龄FMR1基因敲除型(KO)(KO2W、KO4W、KO6W)和同龄野生型(WT)(WT2W、WT4W、WT6W)小鼠大脑纹状皮质、颞听皮质、梨状皮质及海马CA1区、CA3区、齿状回中PV的表达(n=6);应用Western blot法检测上述小鼠大脑皮层、海马组织PV的含量(n=6). 结果 KO2W、KO44W小鼠的大脑纹状皮质、颞听皮质、梨状皮质、海马CA1和CA3区PV阳性中间神经元的数量分别较WT2W、WT4-小鼠减少,差异有统计学意义(P<0.05);KO2W和KO4W小鼠大脑皮层、海马中PV含量分别较WT2W、WT4W小鼠减少,差异有统计学意义(P<0.05). 结论 PV阳性中间神经元及PV含量的减少.可能是引起FXS模型鼠癫痫易感性增加的主要原因.
目的 探討微白蛋白(PV)暘性中間神經元在脆性X綜閤徵(FXS)癲癇易感性增加中的作用. 方法 應用免疫組織化學染色檢測FVB近交繫雄性2、4、6 W齡FMR1基因敲除型(KO)(KO2W、KO4W、KO6W)和同齡野生型(WT)(WT2W、WT4W、WT6W)小鼠大腦紋狀皮質、顳聽皮質、梨狀皮質及海馬CA1區、CA3區、齒狀迴中PV的錶達(n=6);應用Western blot法檢測上述小鼠大腦皮層、海馬組織PV的含量(n=6). 結果 KO2W、KO44W小鼠的大腦紋狀皮質、顳聽皮質、梨狀皮質、海馬CA1和CA3區PV暘性中間神經元的數量分彆較WT2W、WT4-小鼠減少,差異有統計學意義(P<0.05);KO2W和KO4W小鼠大腦皮層、海馬中PV含量分彆較WT2W、WT4W小鼠減少,差異有統計學意義(P<0.05). 結論 PV暘性中間神經元及PV含量的減少.可能是引起FXS模型鼠癲癇易感性增加的主要原因.
목적 탐토미백단백(PV)양성중간신경원재취성X종합정(FXS)전간역감성증가중적작용. 방법 응용면역조직화학염색검측FVB근교계웅성2、4、6 W령FMR1기인고제형(KO)(KO2W、KO4W、KO6W)화동령야생형(WT)(WT2W、WT4W、WT6W)소서대뇌문상피질、섭은피질、리상피질급해마CA1구、CA3구、치상회중PV적표체(n=6);응용Western blot법검측상술소서대뇌피층、해마조직PV적함량(n=6). 결과 KO2W、KO44W소서적대뇌문상피질、섭은피질、리상피질、해마CA1화CA3구PV양성중간신경원적수량분별교WT2W、WT4-소서감소,차이유통계학의의(P<0.05);KO2W화KO4W소서대뇌피층、해마중PV함량분별교WT2W、WT4W소서감소,차이유통계학의의(P<0.05). 결론 PV양성중간신경원급PV함량적감소.가능시인기FXS모형서전간역감성증가적주요원인.
Objective To explore the possible role of parvalbumin (PV)-positive interneuron in the pathogenesis of increased susceptibility to epileptic seizures in FMR1 gene knockout (FMR1 KO)mice. Methods Immunohistochemistry was employed to determine the expression of PV in CA1 and CA3 regions of the hippocampus, the striate cortex, the temporal auditory cortex and the piriform cortex of FVB strain FMR1 KO mice and wild type (WT) controls at the age of 2, 4 and 6 w. Western blotting was used to detect the level of PV in the cerebral cortex and hippocampus of the above mice. Results The numbers of PV-positive interneuron in CA1 and CA3 regions of the hippocampus, the striate cortex,the temporal auditory cortex and the piriform cortex of FMR1 KO mice at the age of 2 and 4 w were significantly decreased as compared with those in the age-matched WT mice (P<0.05). The level of PV in the cerebral cortex and hippocampus in FMR1 KO mice at the age of 2 and 4 w was also significantly decreased than that in the age-matched WT mice (P<0.05). Conclusion Decreased numbers of PV-positive interneuron and level of PV might induce the increased susceptibility to epileptic seizures inFMR1 KO mice.