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作 者:贾乐文[1,2] 李春梅[1,2] 王英德[1,2] 侯金萍 牟希亚[1,2]
机构地区:[1]大连医科大学附属一院内科 [2]大连医科大学菌毛研究室
出 处:《基础医学与临床》1999年第1期73-77,83,共6页Basic and Clinical Medicine
摘 要:为研究绿脓杆菌MSHA菌苗(简称PA-MSHA菌苗)对大鼠实验性免疫损伤性肝纤维化的防治作用及其机理。本文用人血清白蛋白(HSA)致敏、攻击的方法建立一组肝纤维化大鼠模型,作为损伤组,另外建立一组经HSA致敏同时皮下注射PA-MSHA菌苗的大鼠模型作为保护组,并设正常对照组,结果发现,保护组血清β-NAG酶活性(76.7±5.3u/L)较损伤组(94.3±6.3u/L)显著降低(P<0.01);用菌苗保护后的大鼠血清肿瘤坏死因子(TNF)(0.348±0.075ng/mL)显著高于损伤组(0.211±0.029ng/mL,p<0.01):PA-MSHA菌苗能明显抑制Ⅰ、Ⅱ、Ⅲ型胶原及层粘蛋白在肝内沉积(P均<0.01);肝细胞超微结构显示了保护组肝细胞萎缩也减轻。提示,PA-MSHA菌苗对实验性肝纤维化具有显著预防和治疗作用。To study on the mechanism of anti-hepatic fibrosis of Pseudomons Aeruginosa MSHA vaccine (PA-MSHA) preparation on the HSA-immune-induced liver fibrosis of rat models . These rats were divided into the injury group which were established by HSA infection, the protection group pro- tected by PA-MSHA vaccine and the normal group.The results showed:PA-MSHA could remarkablly decrease the activity of serum β-NAGase (76.7 ±5.3u/L) and significantly elevate serum TNF level (0.384 ± 0.075ng/mL) by stimulating the immune cells in comparison with the rats induced HSA (P<0.0 1) . Immunohistochemical finding indicated that PA-MSHA could significantly suppress the deposition of collagen type ⅠⅡD ,Ⅶ and Laminin in the liver with the rat models. PA-MSHA could also protect the hepatocytes from immune injury at the ultrastructrue level . It sugguested that PA- MSHA may have protectively effect on the experimental hepatic fibrosis .
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