实验动物科学 ›› 2021, Vol. 38 ›› Issue (3): 17-.

• 研究报告 • 上一篇    下一篇

耐辐射奇球菌急性毒性研究

  

  1. ( 1. 中国人民解放军新疆军区总医院,新疆特殊环境医学重点实验室,乌鲁木齐 830000) ( 2. 中国人民解放军陆军第九四八医院,乌苏833000) ( 3. 新疆农业大学科学技术学院,乌鲁木齐830091) ( 4. 新疆特殊环境微生物重点实验室,新疆农业科学院微生物应用研究所,乌鲁木齐830091)



  • 出版日期:2021-08-06 发布日期:2021-08-23

Study on Acute Toxicity of Deinococcus radiodurans 

  1. ( 1. General Hospital of Xinjiang Military CommandKey Laboratory of Special Environmental Medicines of XinjiangUrumqi 830000, China)( 2. The 948th Army Hospital of PLAWusu 833000, China) ( 3. Sciences and Technology CollegeXinjiang Agricultural University,Urumqi 830091, China) ( 4. Institute of Applied MicrobiologyXinjiang Academy of Agricultural SciencesThe Key Laboratory of Special Environmental Microorganism of XinjiangUrumqi 830091, China)
  • Online:2021-08-06 Published:2021-08-23

摘要:

摘要:目的 探讨耐辐射奇球菌( Deinococcus radiodurans,DR)活菌及细菌破碎物的急性毒性方法 分别将 DR 浓度 1×109 / mL(高浓度活菌组) 、低浓度 1×107 / mL(低浓度活菌组) 、细菌破碎物高浓度 1× 109 / mL( 高浓度细菌破碎物组) 、低浓度 1×107 / mL(低浓度细菌破碎物组) 0. 4 mL / 10 g 灌胃 KM 小鼠,TGY 培养基组灌胃相同体积的胰蛋白胨葡萄糖酵母琼脂培养基( tryptone glucose yeast agar medium) ,间隔 8 h,灌胃 2 次后,观察 14 d,以小鼠行为脏器系数体质量血常规(白细胞淋巴细胞红细胞血红蛋白红细胞压积平均红细胞体积血小板) 以及血浆生化指标(谷丙转氨酶谷草转氨酶总蛋白肌酐肌酸激酶肌酸激酶 MB 型同工酶乳酸脱氢酶) 变化作为评判依据,比较分析耐辐射奇球菌的毒性结果 不同剂量组的小鼠,均未见分泌物大小便呼吸及运动异,灌胃后 0. 5 h 至实验结束,未观察到反应迟钝瞳孔改变眼球凸出眼睑下垂皮肤颜色改变等异常,受试小鼠体质量血常规和血液生化指标与 TGY 培养基组比较,无显著差异,脾脏系数在低浓度细菌破碎物组有显著增大,病理学检查,未见实质性病变结论 DR 活菌及其细菌破碎物对小鼠无急性毒性,DR 在临床中的拓展应用提供实验依据

关键词: 耐辐射奇球菌, 脏器系数生化指标小鼠, 急性毒性

Abstract:

Abstract: Objective To investigate the acute toxicity of Deinococcus radiodurans ( DR) and its broken products. Method The KM mice were administrated with 0. 4 mL / 10 g of 1×109 / mL DR ( high concentration DR group) , 1×107 / mL DR ( low concentration DR group) , 1 × 109 / mL DR broken products ( high concentration DR debris group) , 1×107 / mL DR broken products ( low concentration DR debris group) and Tryptone Glucose Yeast agar medium ( TGY medium group) , respectively. After intragastrically administrated twice a day every 8 hours, the mice were observed for 14 days, then the organ coefficient, body weight, blood routine ( white blood cell, lymphocyte, red blood cell, hemoglobin, hematocrit, mean corpuscular volume, platelet) and plasma biochemical indexes ( alanine aminotransferase, aspartate aminotransferase, total protein, creatinine, creatine kinase, magnesium, phosphorus, creatine kinase MB isoenzyme, lactate dehydrogenase) were used to analyze and evaluate the toxicity of DR. Result No abnormal secretion, defecation, respiration and movement were found in mice in different dose groups. From 0. 5 hour after administration to the end of the experiment, no abnormalities such as slow reaction, pupil change, eyeball protrusion, eyelid ptosis and skin color change were observed in the test mice.There were no significant differences in body weight, blood routine test and blood biochemical indexes in the trialgroups compared with TGY group. The spleen coefficient was significantly increased in the low-dose group, and the spleen pathological examination showed that there was no substantial lesion. Conclusion The live and broken DR have no acute toxicity to mice. This experiment provides experimental basis for clinical application of DR.