中华实用儿科临床杂志
中華實用兒科臨床雜誌
중화실용인과림상잡지
Journal of Applied Clinical Pediatrics
2015年
12期
900-903
,共4页
王雪莹%黄绍平%宋婷婷%李丹%杨琳
王雪瑩%黃紹平%宋婷婷%李丹%楊琳
왕설형%황소평%송정정%리단%양림
环氧化酶-2选择性抑制剂%癫(癎)持续状态%P-糖蛋白
環氧化酶-2選擇性抑製劑%癲(癎)持續狀態%P-糖蛋白
배양화매-2선택성억제제%전(간)지속상태%P-당단백
Cyclooxygenase-2 selective inhibitors%Status epilepticus%P-glycoprotein
目的 研究环氧化酶-2(COX-2)选择性抑制剂塞来考昔对癫(癎)持续状态大鼠脑组织中P-糖蛋白(P-gp)表达的影响,为寻找治疗难治性癫(癎)的新药物提供理论依据.方法 健康成年雄性SD大鼠60只按随机数字表法随机分为空白对照组、癫(癎)模型组和塞来考昔干预组.氯化锂-毛果芸香碱诱发SD大鼠癫(癎)持续状态,48只纳入实验,每组16只.各实验组均采用免疫组织化学法和Western blot法检测鼠额叶皮质区及海马区P-gp的表达情况.结果 免疫组织化学结果显示:与空白对照组比较,癫(癎)模型组中P-gp的表达显著增高,差异有统计学意义(P<0.01);塞来考昔干预后的大鼠脑组织P-gp较癫(癎)模型组显著下降,差异有统计学意义(P<0.01).Western blot法检测结果提示:各组额叶皮层和海马中均有P-gp的表达.与空白对照组比较,癫(癎)模型组中P-gp的表达量显著增高,差异有统计学意义(P<0.01);塞来考昔干预组大鼠脑组织P-gp的表达量较癫(癎)模型组显著下降,差异有统计学意义(P<0.05).结论 COX-2抑制剂塞来考昔可降低P-gp在癫(癎)持续状态大鼠脑组织中的表达,有望成为治疗难治性癫(癎)的新方法.
目的 研究環氧化酶-2(COX-2)選擇性抑製劑塞來攷昔對癲(癎)持續狀態大鼠腦組織中P-糖蛋白(P-gp)錶達的影響,為尋找治療難治性癲(癎)的新藥物提供理論依據.方法 健康成年雄性SD大鼠60隻按隨機數字錶法隨機分為空白對照組、癲(癎)模型組和塞來攷昔榦預組.氯化鋰-毛果蕓香堿誘髮SD大鼠癲(癎)持續狀態,48隻納入實驗,每組16隻.各實驗組均採用免疫組織化學法和Western blot法檢測鼠額葉皮質區及海馬區P-gp的錶達情況.結果 免疫組織化學結果顯示:與空白對照組比較,癲(癎)模型組中P-gp的錶達顯著增高,差異有統計學意義(P<0.01);塞來攷昔榦預後的大鼠腦組織P-gp較癲(癎)模型組顯著下降,差異有統計學意義(P<0.01).Western blot法檢測結果提示:各組額葉皮層和海馬中均有P-gp的錶達.與空白對照組比較,癲(癎)模型組中P-gp的錶達量顯著增高,差異有統計學意義(P<0.01);塞來攷昔榦預組大鼠腦組織P-gp的錶達量較癲(癎)模型組顯著下降,差異有統計學意義(P<0.05).結論 COX-2抑製劑塞來攷昔可降低P-gp在癲(癎)持續狀態大鼠腦組織中的錶達,有望成為治療難治性癲(癎)的新方法.
목적 연구배양화매-2(COX-2)선택성억제제새래고석대전(간)지속상태대서뇌조직중P-당단백(P-gp)표체적영향,위심조치료난치성전(간)적신약물제공이론의거.방법 건강성년웅성SD대서60지안수궤수자표법수궤분위공백대조조、전(간)모형조화새래고석간예조.록화리-모과예향감유발SD대서전(간)지속상태,48지납입실험,매조16지.각실험조균채용면역조직화학법화Western blot법검측서액협피질구급해마구P-gp적표체정황.결과 면역조직화학결과현시:여공백대조조비교,전(간)모형조중P-gp적표체현저증고,차이유통계학의의(P<0.01);새래고석간예후적대서뇌조직P-gp교전(간)모형조현저하강,차이유통계학의의(P<0.01).Western blot법검측결과제시:각조액협피층화해마중균유P-gp적표체.여공백대조조비교,전(간)모형조중P-gp적표체량현저증고,차이유통계학의의(P<0.01);새래고석간예조대서뇌조직P-gp적표체량교전(간)모형조현저하강,차이유통계학의의(P<0.05).결론 COX-2억제제새래고석가강저P-gp재전(간)지속상태대서뇌조직중적표체,유망성위치료난치성전(간)적신방법.
Objective To study the effect of cyclooxygenase-2 (COX-2)selective inhibitor Celecoxib on the expression of P-glycoprotein(P-gp)in the brain of rats with status epilepficus,in order to assess the therapeutic value of intractable epilepsy.Methods Sixty adult male SD rats were randomly divided into blank control group,the epilepsy model group and Celecoxib intervention group.The status epilepticus was induced in rats by injecting Lithium pilocarpine.Forty-eight rats were included in the experiment.There were 16 rats in each of the blank control group,epilepsy model group and Celecoxib intervention group,respectively.Immunohistochemical method and Western blot method were used to detect the expression of P-gp in experimental group in the frontal cortex and hippocampus.Results Immunohistochemistry result showed that the expression of P-gp was significantly higher in epilepsy model group than the blank control group,and the difference was statistically significant (P < 0.01);The P-gp expression in the Celecoxib intervention group was lower than that in the epilepsy model group,and the difference was statistically significant (P <0.01).Western blot results suggested that the expression of P-gp could be found both in the frontal cortex and hippocampus in each group.Compared with the blank control group,the P-gp expression was significantly higher than that in the epilepsy model group,and the expression of the P-gp was lower after the Celecoxib intervention than that in the epilepsy model group,and the difference was statistically significant (P < 0.05).Conclusions COX-2 inhibitor Celecoxib could decrease the expression of P-gp in brain tissue with status epilepticus,which may provide a new method for the treatment of intractable epilepsy.