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作 者:黄未劼 张同辉[2] 蔡泽宇 庞聪[2] 沈枕 方攀 潘经媛[2] HUANG Weijie;CAI Zeyu;PANG Cong;SHEN Zhen;FANG Pan;PAN Jingyuan(2.Hubei Institute Co.,Ltd of Pharmaceutical Industry,Wuhan 430061,China;Wuhan Shuanglong Pharmaceutical Co.,Ltd,Wuhan 430075,China)
机构地区:[1]武汉大学药学院,武汉430071 [2]湖北省医药工业研究院有限公司,武汉430061 [3]武汉双龙药业有限公司,武汉430075
出 处:《医药导报》2019年第3期321-327,共7页Herald of Medicine
摘 要:目的考察柴连感冒颗粒对大鼠的长期毒性,为其临床安全用药提供实验依据。方法将120只SD大鼠随机分为柴连感冒颗粒大、中、小剂量组(均灌胃给予柴连感冒颗粒,剂量以生药计分别为45.0,24.0,12.0 g·kg-1)及溶媒对照组(灌胃给予纯化水),每组30只,雌雄各半,20 mL·kg-1·d-1,qd,连续31 d。观察给药期间和停药14 d后大鼠的一般状况及体质量、血液学、血液生化学、脏器系数及病理组织学变化。结果与同期溶媒对照组比较,柴连感冒颗粒大剂量组体质量增长减缓,给药第7天与第14天摄食量减少,胸腺系数降低,肝脏和肾上腺系数增加,胆固醇降低,停药后逐渐恢复正常;柴连感冒颗粒中小剂量组大鼠体质量、摄食量、血液学、血液生化指标、脏器系数和病理学检查未见明显异常。结论在该实验条件下,柴连感冒颗粒对大鼠重复灌胃给药31 d的无毒反应剂量为24.0 g·kg-1,相当于临床拟用剂量的28倍。Objective To observe the long-term toxicity of Chailian Ganmao granules on rats to provide a scientific experimental basis for clinical treatment. Methods Totally, 120 SD rats were randomly divided into high, middle, low dose Chailian Ganmao granules groups and solvent control group.They were intragastrically administered with Chailian Ganmao Granules at 45.0, 24.0 and 12.0 g·kg -1 (in crude drugs), and 20 mL·kg -1 ·d -1 pure water, respectively daily for 31 d. The general condition of rats and body weight, the hematology index, blood biochemistry index, viscera coefficient and histopathological changes during administration and 14 d after drug withdrawal were observed. Results In comparison with the solvent control group, the growth of body mass was reduced in the high dose group, food consumption only in the 7th and 14th day decreased, the coefficient of thymus gland reduced, the coefficient of liver and adrenal gland increased, cholesterol decreased, and gradually recovered after drug withdrawal.The body weight, food intake, hematology index, blood biochemical parameters, organ coefficient and pathological examination indexes of rats were not changed significantly. Conclusion Under the experimental conditions, the non-toxic reaction dose of Chailian Ganmao granules is considered to be 24.0 g·kg -1 (28 times as much as the clinical dosage) for 31 d in rats.
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