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作 者:孙全文[1,2] 张丹参[2] 薛桂平[2] 李凤学[2] 吴淑琴[2] 乔健[1]
机构地区:[1]中国农业大学动物医学院,北京100193 [2]河北北方学院,河北张家口075000
出 处:《Agricultural Science & Technology》2010年第3期110-114,共5页农业科学与技术(英文版)
摘 要:[Objective] The research aimed to discuss the accumulation of toxic slag of penicillin bacteria residue degradation products and explore its ability to meet the aquaculture industry as a protein feed into development and utilization conditions.[Method] Through the sub-acute toxicity tests in mice strains,which were fed by different doses of penicillin bacteria residue degradation products (3% and 6%) under continuous observation of 15 weeks,recording a weekly mouse weight and death,and sampling executed after the test,animal liver and kidney function were blood test,taking heart,liver,spleen,kidney weighing,as well as liver and kidney pathology observed in the optical microscope.[Result] There were no significant differences (P 0.05) between the test group mice body weight,mortality and liver and kidney function and the control group within 15 weeks.Low-dose test group could be seen the liver cells,renal tubular epithelial nuclei broken,and a small number of liver and kidney cells with mild edema.High-dose test group could be seen in liver tissue of mice nuclei fragmentation and a fat droplets,the majority of liver cells,edema,and only a small number of liver cells,there were no significant changes.Renal portal area showed inflammatory cell infiltration,renal tubular epithelial cells,edema and necrosis.[Conclusion] In this experimental condition,the degradation products of penicillin bacteria residue played a mild toxcity on organ parenchymal cells in mice.[目的]初步研究青霉素菌渣残留降解物的蓄积毒性,进而探讨其是否具备作为蛋白饲料投入养殖业开发利用的条件。[方法]通过小鼠亚急性毒性试验,饲喂小鼠不同剂量的青霉素菌渣降解物(3%和6%)连续观察15周,记录每周小白鼠的体重和死亡情况;试验结束后抽样处死,取血测动物肝、肾功能,取心、肝、脾、肾称重,并在光镜下对肝、肾组织做病理学观察。[结果]试验组小白鼠体重、死亡率及肝、肾功能在15周内和对照组差异均不显著(P>0.05)。低剂量组可见肝细胞、肾小管上皮细胞核有碎裂,少数肝、肾细胞有轻度水肿;高剂量组可见小白鼠肝组织中细胞核碎裂并有脂肪滴,多数肝细胞水肿,只有少数肝细胞无明显改变;肾脏可见门管区炎性细胞浸润,肾小管上皮细胞水肿、坏死。[结论]该实验条件下青霉素菌渣降解物对小鼠器官的实质细胞有轻度的毒性作用。
关 键 词:Residue degradation products of penicillin bacteria Mice Subacute toxicity PATHOLOGY
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