中华神经科杂志
中華神經科雜誌
중화신경과잡지
Chinese Journal of Neurology
2010年
11期
791-794
,共4页
伍国锋%宋安军%蒋乃昌%马莉
伍國鋒%宋安軍%蔣迺昌%馬莉
오국봉%송안군%장내창%마리
癫(癎)%海马%神经元%钙%电生理学%流式细胞术%大鼠
癲(癎)%海馬%神經元%鈣%電生理學%流式細胞術%大鼠
전(간)%해마%신경원%개%전생이학%류식세포술%대서
Epilepsy%Hippocampus%Neurons%Calcium%Electrophysiology%Flow cytometry%Rats
目的 探讨癫(癎)大鼠海马细胞内Ca2+浓度变化和神经元单位放电的关系.方法36只Wistar雄性健康大鼠分为3组.癫(癎)模型组用青霉素钠600万U/kg腹腔注射制作成癫(癎)模型;癫(癎)预处理组在制作模型前用盐酸氟桂利嗪按20 mg/kg间隔12 h灌胃2次,第2次给药后2 h用青霉素钠600万U/kg腹腔注射制作模型.3组实验大鼠均在记录单位放电后处死,取双侧海马应用新一代钙荧光指示剂Fluo-3-AM通过流式细胞分析仪测定细胞内Ca2+荧光浓度.结果 正常对照组大鼠共记录到24个单位海马神经元放电,海马细胞内Ca2+平均荧光浓度为37.12±5.08;癫(癎)模型组共记录到78个单位海马神经元放电,海马细胞内Ca2+平均荧光浓度为52.04±6.75;癫(癎)预处理组共记录到47个单位海马神经元放电,海马细胞内Ca2+平均荧光浓度为37.79±3.09.Ca2+平均荧光值和海马单位放电个数相关系数r=0.737,P<0.01.结论 青霉素致病大鼠海马细胞内Ca2+浓度变化与海马神经元单位放电呈正相关关系.
目的 探討癲(癎)大鼠海馬細胞內Ca2+濃度變化和神經元單位放電的關繫.方法36隻Wistar雄性健康大鼠分為3組.癲(癎)模型組用青黴素鈉600萬U/kg腹腔註射製作成癲(癎)模型;癲(癎)預處理組在製作模型前用鹽痠氟桂利嗪按20 mg/kg間隔12 h灌胃2次,第2次給藥後2 h用青黴素鈉600萬U/kg腹腔註射製作模型.3組實驗大鼠均在記錄單位放電後處死,取雙側海馬應用新一代鈣熒光指示劑Fluo-3-AM通過流式細胞分析儀測定細胞內Ca2+熒光濃度.結果 正常對照組大鼠共記錄到24箇單位海馬神經元放電,海馬細胞內Ca2+平均熒光濃度為37.12±5.08;癲(癎)模型組共記錄到78箇單位海馬神經元放電,海馬細胞內Ca2+平均熒光濃度為52.04±6.75;癲(癎)預處理組共記錄到47箇單位海馬神經元放電,海馬細胞內Ca2+平均熒光濃度為37.79±3.09.Ca2+平均熒光值和海馬單位放電箇數相關繫數r=0.737,P<0.01.結論 青黴素緻病大鼠海馬細胞內Ca2+濃度變化與海馬神經元單位放電呈正相關關繫.
목적 탐토전(간)대서해마세포내Ca2+농도변화화신경원단위방전적관계.방법36지Wistar웅성건강대서분위3조.전(간)모형조용청매소납600만U/kg복강주사제작성전(간)모형;전(간)예처리조재제작모형전용염산불계리진안20 mg/kg간격12 h관위2차,제2차급약후2 h용청매소납600만U/kg복강주사제작모형.3조실험대서균재기록단위방전후처사,취쌍측해마응용신일대개형광지시제Fluo-3-AM통과류식세포분석의측정세포내Ca2+형광농도.결과 정상대조조대서공기록도24개단위해마신경원방전,해마세포내Ca2+평균형광농도위37.12±5.08;전(간)모형조공기록도78개단위해마신경원방전,해마세포내Ca2+평균형광농도위52.04±6.75;전(간)예처리조공기록도47개단위해마신경원방전,해마세포내Ca2+평균형광농도위37.79±3.09.Ca2+평균형광치화해마단위방전개수상관계수r=0.737,P<0.01.결론 청매소치병대서해마세포내Ca2+농도변화여해마신경원단위방전정정상관관계.
Objective To investigate the relationship between changes in Ca2+ concentration and unit discharge in the hippocampal neurons of epileptic rats.Methods Thirty-six healthy male Wistar rats were divided into three groups. Rats of the epilepsy group received an intraperitoneal injection of benzylpenicllin sodium at 6 million unit/kg; Rats of the epilepsy pretreatment group received 20 mg/kg of flunarizine at 14 and 2 hours before injection of benzylponicllin;the control group of rats received an intraperitoneal injection of normal saline.Three groups of rats were euthanized after recording of the unit discharge,and bilateral hippocampal cells were obtained to measure the cellular concentration of Ca2+ fluorescence using the new generation Ca2+ fluorescent dye Fluo-3-AM and flow cytometry.Results (1) A total of 24 units of hippocampal discharges were recorded in the control group.The average concentration Ca2+ fluorescence of the hippocampal neurons was 37.12±5.08.(2)A total of 78 units of hippocampal discharges were recorded in the epilepsy group.The average concentration of Ca2+fluorescence of the hippocampal neurons was 52.04±6.75.(3)A total of 47 units of hippocampal discharges were recorded in the epilepsy pretreatment group. The average concentration of Ca2+ fluorescence of the hippocampal neurons was 37.79±3.09.The correlation coefficient between the average concentration of Ca2+ fluorescence of the hippocampal neurons and the number of units of hippocampal discharge ( r=0.737,P<0.01).Conclusion There is a positive correlation between changes in average concentration of Ca2+ fluorescence of the hippocampal neurons and the numbers of units of hippocampal discharge.