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作 者:张星宇[1] 陈曙霞[2] 刘晶星[3] 钱富荣[2]
机构地区:[1]上海交通大学医学院附属仁济医院急诊科,上海200127 [2]上海交通大学医学院附属仁济医院心内科,上海200127 [3]上海交通大学基础医学院微生物教研室,上海200025
出 处:《中国新药与临床杂志》2006年第9期709-712,共4页Chinese Journal of New Drugs and Clinical Remedies
摘 要:目的:应用柯萨奇病毒B3(CVB3)感染SD大鼠乳鼠心肌细胞造成病毒性心肌炎模型,观察槐果碱对该模型的作用。方法:(1)将乳鼠心肌细胞分成4组:感染组,感染CVB3;治疗组,感染病毒后加入100mg·L^(-1)的槐果碱;同时设立药物对照组和细胞对照组。在处理的d 2,3,5观察各组细胞病变效应(CPE)、细胞搏动频率并测定细胞上清液中乳酸脱氢酶浓度。(2)将心肌细胞感染CVB3后加入不同浓度的槐果碱(12.5~400mg·L^(-1)),设立病毒、细胞及药物对照。在处理后d 2,3,5观察CPE并测定细胞上清中的乳酸脱氢酶(LDH)浓度。结果:(1)100mg·L^(-1)的槐果碱对感染CVB3的乳鼠心肌细胞有保护作用,治疗组的CPE较感染组减轻,上清液中的LDH浓度降低。(2)槐果碱在12.5~300mg·L^(-1)之间均对感染CVB3的乳鼠心肌细胞有保护作用,它可以减轻病毒导致的CPE,并减少LDH释放。在400mg·L^(-1)反而会加重CPE,增加LDH释放。结论:一定浓度的槐果碱在体外对感染CVB3的心肌细胞有保护作用。AIM: To observe the effect of sophocarpine (SC) on the myocarditis model established by coxsackievirus B3 (CVB3) in cardiomyocytes from neonatal rats. METHODS: Cardiomyocytes from neonatal rats were divided into four groups: infected group, which was infected by CVB3; SC treated group, which was incubated with SC (100 mg.L^-1) after viral infection; SC control group, which was incubated with SC (100 mg. L^-1) only; and cell control group. The cytopathic effect (CPE), beating frequency of myocardial cells and the lactate dehydrogenase (LDH) levels in supernatant was tested at day 2, 3, 5 respectively after the treatment. The cultured myocytes were incubated with different concentrations of SC ( 12.5 - 400 mg.L^-1) after infected by CVB3. The CPE and the levels of LDH were tested at day 2, 3, 5 after treatment. RESULTS: (1) SC had protective effect on CVB3-infectcd cardiomyocytes. The cytopathic effect was lighter and the LDH level was lower in SC treated group (100 mg.L^-1) than that in infected group. (2) SC in concentration between 12.5 - 300 mg. L^-1 could protect the cardiomyocytes from CVB3; it improved CPE and decreased the LDH levels. While in a higher concentration (400 mg.L^-1) , SC exacerbated the CPE and increased LDH levels. CONCLUSION: SC in certain concentration could protect cardiomyocytes from CVB3 in vitro.
分 类 号:R373.23[医药卫生—病原生物学] R542.21[医药卫生—基础医学]
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