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作 者:陈敬国[1] 方慧云[1] 蒋犁[2] 程敏婷[1]
机构地区:[1]广东省中山市人民医院,528403 [2]东南大学医学院附属中大医院,江苏南京210009
出 处:《时珍国医国药》2007年第2期F0003-F0004,共2页Lishizhen Medicine and Materia Medica Research
摘 要:目的探讨缺氧缺血脑损伤对新生大鼠HIBD脑皮质IL-6放射免疫浓度,Fas-L蛋白表达的影响,及清开灵对新生大鼠HIBD的干预治疗作用以及有关分子机制。方法建立HIBD动物模型后分为放射免疫法测定组和免疫组化测定组,每组又分为清开灵干预组、生理盐水对照组、假手术组,根据检测需要,在缺氧缺血后24 h,3 d,7 d作IL-6脑皮质匀浆放射免疫浓度测定、Fas-L蛋白免疫组化SP法测定。结果①脑皮质组织匀浆IL-6放射免疫浓度(pg/ml)假手术组、生理盐水组、清开灵干预组:24 h依次为50.1±6.2,56.3±7.1,51.3±6.8;3 d依次为50.6±6.4,250.3±11.2,78.1±8.3;7 d依次为51.4±6.6,345.7±12.3,81.2±9.2,生理盐水组与另两组分别比较,24 hP均>0.05,无明显变化;3,7d生理盐水组增加明显?P<0.05)清开灵干预组降低明显?P<0.05)。②③④左脑皮质Fas-L蛋白表达阳性率假手术组、生理盐水组、清开灵干预组:24 h依次为8.04±3.50,120.20±6.10,21.10±5.10;3 d依次为8.20±3.10,87.6±5.90,13.40±4.20;7 d依次为8.01±2.80,8.32±2.90,8.26±2.83;生理盐水组与另两组分别比较,7 dP均>0.05,无明显变化;24 h,3 d增多明显(P<0.05),清开灵干预组降低明显(P<0.05)。结论①新生大鼠HIBD后24 h,3 d,7 d脑皮质IL-6含量逐渐增高。②清开灵能降低新生大鼠HIBD脑皮质IL-6的产生量。③新生大鼠HIBD后,结扎侧脑皮质fas-L蛋白表达增高。④清开灵能抑制新生大鼠HIBD结扎侧脑皮质fas-L蛋白的高表达。Objective To explore the immunologic changes of interleukin -6 (IL- 6) , the expression of fas- L protein of cortex in newborn rats after HIBD and the effects of QingKaiLing on them. Methods To divide animals for experiment into groups: IL - 6 test group: Animals were divided into sham group, NS group and QingKailing group, IL- 6 radioimmunologic concentrations of cortex were measured at 24 h, 3d and 7d after hypoxia ischemia by radioimmunoassay. Immunohistochemistry. group: Animals were divided into sham group, NS group and QingKaiLing group. The changes of expression of fas - L protein were detected at 24h, 3d and 7d after hypoxia ischemia by immunohistochemistry. Results Comparing with the sham group, the concentration of IL -6 and the expression of fas -L protein (at 24h, 3d and 7d) increased obviously in the ligated side of the brain cortex in NS group (P 〈0.05 ) . Comparing with NS group, they were on the contrary in QingKaiLing group(P 〈 0.05). Conclusion The concentration of IL-6, the expression of fas -L protein become higher rapidly after HIBD. QingKaiLing can inhibit the production of IL -6 and the expression of fas - L protein.
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