中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2013年
2期
119-122
,共4页
张雪峰%王峰%苗露%宋子木%王恩杰%徐进%孙涛
張雪峰%王峰%苗露%宋子木%王恩傑%徐進%孫濤
장설봉%왕봉%묘로%송자목%왕은걸%서진%손도
岛叶%杏仁核%海马%点燃%活性调节细胞骨架蛋白
島葉%杏仁覈%海馬%點燃%活性調節細胞骨架蛋白
도협%행인핵%해마%점연%활성조절세포골가단백
Insular cortex%Amygdala%Hippocampus%Kindling%Activity-regulated cytoskeleton-associated protein
目的 探讨岛叶在杏仁核点燃大鼠癫痫发作中的作用. 方法 健康雄性SD大鼠48只,按照随机数字表法分为空白组(n=8)、假手术组(n=8)和点燃组(n=32),点燃组以最后一次刺激为零点,再分为点燃后1h、3h、6h、12h4个亚组,每亚组8只.空白组不做任何处理;假手术组植入电极后不予刺激;点燃组植入电极后予以电刺激,制作杏仁核点燃模型.采用荧光原位杂交和免疫组化检测大鼠海马、岛叶脑区活性调节细胞骨架蛋白(Arc) mRNA和蛋白表达的变化. 结果 点燃大鼠海马、岛叶的Arc mRNA在点燃后1h开始增高,3h达到高峰,与空白组、假手术组比较,差异均有统计学意义(P<0.05);6 h时回到正常水平.Arc蛋白在点燃后3h开始增高,6h达到高峰,与空白组、假手术组比较,差异均有统计学意义(P<0.05);12h时回到正常水平.假手术组与空白组之间Arc mRNA和蛋白差异没有统计学意义(P>0.05). 结论 岛叶与杏仁核、海马构成了一个灶性复合体,共同参与了颞叶癫痫的发生.
目的 探討島葉在杏仁覈點燃大鼠癲癇髮作中的作用. 方法 健康雄性SD大鼠48隻,按照隨機數字錶法分為空白組(n=8)、假手術組(n=8)和點燃組(n=32),點燃組以最後一次刺激為零點,再分為點燃後1h、3h、6h、12h4箇亞組,每亞組8隻.空白組不做任何處理;假手術組植入電極後不予刺激;點燃組植入電極後予以電刺激,製作杏仁覈點燃模型.採用熒光原位雜交和免疫組化檢測大鼠海馬、島葉腦區活性調節細胞骨架蛋白(Arc) mRNA和蛋白錶達的變化. 結果 點燃大鼠海馬、島葉的Arc mRNA在點燃後1h開始增高,3h達到高峰,與空白組、假手術組比較,差異均有統計學意義(P<0.05);6 h時迴到正常水平.Arc蛋白在點燃後3h開始增高,6h達到高峰,與空白組、假手術組比較,差異均有統計學意義(P<0.05);12h時迴到正常水平.假手術組與空白組之間Arc mRNA和蛋白差異沒有統計學意義(P>0.05). 結論 島葉與杏仁覈、海馬構成瞭一箇竈性複閤體,共同參與瞭顳葉癲癇的髮生.
목적 탐토도협재행인핵점연대서전간발작중적작용. 방법 건강웅성SD대서48지,안조수궤수자표법분위공백조(n=8)、가수술조(n=8)화점연조(n=32),점연조이최후일차자격위영점,재분위점연후1h、3h、6h、12h4개아조,매아조8지.공백조불주임하처리;가수술조식입전겁후불여자격;점연조식입전겁후여이전자격,제작행인핵점연모형.채용형광원위잡교화면역조화검측대서해마、도협뇌구활성조절세포골가단백(Arc) mRNA화단백표체적변화. 결과 점연대서해마、도협적Arc mRNA재점연후1h개시증고,3h체도고봉,여공백조、가수술조비교,차이균유통계학의의(P<0.05);6 h시회도정상수평.Arc단백재점연후3h개시증고,6h체도고봉,여공백조、가수술조비교,차이균유통계학의의(P<0.05);12h시회도정상수평.가수술조여공백조지간Arc mRNA화단백차이몰유통계학의의(P>0.05). 결론 도협여행인핵、해마구성료일개조성복합체,공동삼여료섭협전간적발생.
Objective To investigate the role of insular cortex in amygdala-kindled seizures in rats.Methods Forty-eight healthy male SD rats were randomly divided into blank control group (n=8),sham-operated group (n=8) and amygdala-kindled group (n=32); no treatment was performed in the blank control group,and only implantation of electrodes was performed in the sham-operated group; implantation of electrodes and electrophotoluminescence were performed in the amygdala-kindled group to induce amygdala-kindled seizure models.Rats in the amygdala-kindled group was divided into 4sub-groups (n=8) at different times after the kindling (1,3,6 and 12 h).Fluorescence in situ hybridization and immunohistochemistry staining were employed to investigate the altered mRNA and protein expressions of activity-regulated cytoskeleton-associated protein (Arc) in the hippocampus and insula of the rat brain.Results As compared with that in the blank control group and sham-operated group,Arc mRNA expression in the amygdala-kindled sub-groups increased at 1 h after the kindling (P<0.05),peaked at 3 h after the kindling (P<0.05),and returned to basic level at 6 h after the kindling (P>0.05).As compared with that in the blank control group and sham-operated group,Arc protein expression in the amygdala-kindled sub-groups increased at 3 h after the kindling,(P<0.05),peaked at 6 h after the kindling (P<0.05),and returned to basic level at 12 h after the kindling (P>0.05).No significant difference on mRNA and protein expressions of Arc was noted between the sham-operated group and blank control group (P>0.05).Conclusion Insular cortex,the amygdala and the hippocampus form a focus complex,which participates in the occurrence of temporal lobe epilepsy.