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出 处:《内科急危重症杂志》2012年第4期212-213,共2页Journal of Critical Care In Internal Medicine
摘 要:目的:研究头孢曲松对脓毒症模型小鼠脾脏树突状细胞(DCs)的影响,及其临床意义。方法:96只雄性昆明鼠随机分配入组,正常对照组(A组)40只、脓毒症模型组(B组)32只、头孢曲松治疗组(C组)24只。采用盲肠结扎穿孔术(CLP)制模,制模后0、12、24、48、72h分批处死小鼠,流式细胞计数脾脏DCs及凋亡率。结果:与正常观察组比较,模型组所有观察时间点脾脏DCs数量明显减少,凋亡率增加(均P﹤0.05);给予头孢曲松治疗后脾脏DCs的丢失进一步加剧(P﹤0.05),但凋亡率无显著改变(P﹥0.05)。结论:严重脓毒症时脾脏DCs明显减少。常规使用头孢曲松加剧DCs的丢失,但凋亡率无显著改变,推测源于单核细胞向DCs的分化障碍,从而加剧了免疫抑制和炎症失衡。Objective: To study the effect of Ceftriaxone on splenic dendritic cells (DCs) in rat model of sepsis and its clinical significance. Methods : Ninety-six male Kunming rats were randomly divided into group A ( control group, n = 40) , group B (sepsis model group, n =32) , group C (Ceftriaxone group, n =24). The rats were sacrificed at 0, 12, 24, 48 and 72 hours after cecal ligation and puncture (CLP) , and the amount and apoptosis of splenic DCs were counted by flow cytometry. Results: The number of DCs decreased and the apoptotic rate increased significantly in CLP group at all time points compared with those of control group ( P 〈 0.05 ). After administration of Ceftriaxone, the loss of splenic DCs con- tinued to aggravated ( P 〈 0.05 ), but the apoptotic rate remained unchanged significantly ( P 〉 0.05 ). Conclusions : The number of splenic DCs decreased markedly during the course of severe sepsis. The routine use of Ceftriaxone further de- creased the number of DCs but without further increasing the apoptosis of DCs, which is presumably due to altered differen- tiation of moncytes to DCs, thus aggravating immunosupprssion and inflammatory imbalance.
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