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利心Ⅰ号对实验性充血性心力衰竭大鼠血浆TNF-α及AngⅡ的影响
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摘要
目的:探讨利心Ⅰ号对充血性心力衰竭大鼠模型血浆TNF-α及Ang-Ⅱ的影响。
     方法:用腹腔注射阿霉素法复制目前公认的Wistar大鼠CHF模型。将84只动物模型随机平均分为中药对照组、西药对照组、中药低剂量组和中药高剂量组四组,进行药效学研究,并设立正常对照组和模型对照组。正常组:自由饮食、水。模型组:灌服0.9%生理盐水。西药对照组:灌服依那普利混悬液。中药对照组:灌服心宝混悬液。中药低剂量组:给予利心Ⅰ号煎剂灌胃,13.0g/kg。中药高剂量组:给予利心Ⅰ号煎剂灌胃,26.0g/kg。以上各组,每日一次,连续灌胃4周后用2%戊巴比妥钠腹腔注射麻醉,颈动脉取血,测定血浆中TNF-α和Ang-Ⅱ含量。
     结果:1、模型组大鼠血浆TNF-α值明显高于正常对照组;各治疗组血浆TNF-α含量与模型组比较均明显降低,其中,中药高剂量组与西药对照组及中药低剂量组比较有显著差异;
     2、模型组大鼠血浆Ang-Ⅱ含量明显高于正常对照组,各治疗组血浆Ang-Ⅱ与模型组比较均明显降低,且中药高剂量组优于中药对照组及中药低剂量组。
     结论:利心Ⅰ号能够降低实验性CHF大鼠血浆TNF-α及AngⅡ水平,以中药高剂量组效果最佳。
Objective: To study the effect of LiXin Ⅰ the a-Tumor Necrosis Factor and Angiotensin Ⅱ gravity of serum of the experimental rat with Congestive Heart Failure..METHODS: Eighty four Wistar rats were selected and divided randomly into six groups :one group of them in the normal control group ;others in the model groups established by intraperitoneal injection of Adriamycin. The later was classified as follow:the control model group admonished with physiological saline ;the XinBao treatment model group admonished with XinBao mixed liquid ;the medicine treatment model group admonished with Enalapril tablet mixed liquid ;the small dose LiXin Ⅰ treatment model group admonished with Li Xin Ⅰ mixed liquid(13.0g/kg) ;the large dose LiXin I treatment group admonished with LiXin I mixed liquid(26.0g/kg). All treatment groups had continually admonished by oral gavage one time a day.food and drink were given as usual.After four weeks,blood was obtained from rat carotid artery under the aneshthesia state and TNF-α and Ang Ⅱ were tested.RESULT:The experiment results show :firstly,TNF-α of serum of rat in the control model group is higher than in the normal control group (p<0.01) . TNF-α of serum of rat in the treatment groups is lower than in the control model group(p<0.01).TNF-α in the large dose LiXin Ⅰ treatment model group is lower than in the small dose LiXin Ⅰ and medicine treatment group respectively.Di-fference between them is obvious(p<0.05). secondly , Ang Ⅱ of serum in the control model group is higher than in the normal contrst group and treatment groups .Ang Ⅱ in the large dose LiXin I treatment group is lower than in the XinBao treatment group and in the small dose LiXin treatment group respectively (p<0.01). CONCLUSION: LiXin Ⅰ can
引文
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