| Objective 1.To establishthe silica-induced pulmonary fibrosis model in rats; 2.To observethe influence of Auricularia auricular powders (AAP) onthe silicosis fibrosis in rats; 3.To explorethe mechanism ofthe effects of model rats bythe histopathology,the activity ofthe SOD,the contents of MDA,NO and HYP. Methods Eighty rats were randomly divided into control group, silica control group, and AAP -treated groupâ…¢,â…¡andâ… . Silicotic control group, AAP -treated groupâ…¢,â…¡andâ… animal models were established by direct tracheal instillation of silica into rat lungs non-surgically. After modeling 24 hours,rats in AAP-treated groupâ…¢,â…¡andâ… were given AAP by feeding. At modeling 14th,56th days establishment ofthe animal model, eight rats were killed in a group at a time and calculate lung/body coefficient. Lung fibrosis in morphology was observed by H.E staining,and collagen content was detected by Hydroxyproline assy. Quantity analysis of fibrosis content by Sirius Red staining and Image analysis system.The superoxide dismutase (SOD) activities, maleic dialdehyde(MDA)content and glutathione peroxidase (NO)content were assayed by colorimetry method. Resultsâ‘´the changes of lung/body coefficient: At 14th day,lung/body coefficient in AAP-treated groups were significantly higherthanthose of SiO2 control group(P<0.05) . lung/body coefficient in AAP-treated groupâ…¢were still significantly lowerthanthose of SiO2 control group(P<0.05). At 56th day,lung/body coefficient in AAP-treated groupâ…¢were still significantly lowerthanthose of SiO2 control group(P<0.01).⑵Pathologic inspection:At 14th , The Pathologic injury degree of 87.5percent rats lung in AAP-treatedâ…¢groups and 25.5percent rats lung in AAP-treatedâ…¡groups was lighter thanthat of SiO2 control group, at 56th day,62.5 percent rats lung in AAP-treatedâ…¢groups was lighterthanthat of SiO2 control group,and lighter l/2 Pathologic grade.â‘¶the changes of fibrosis content: At 14th ,56th day, The fibortic area percentage of rats lung was lower in AAP-treated groups different degreelythanthose of SiO2 control group, AAP-treated groupâ…¢was lowerthanthose of SiO2 control group(P<0.05).â‘·the changes of HYP content:At 14th day,HYP content in AAP-treated groups was lowerthanthose of SiO2 group(P<0.05). HYP content in AAP-treatedâ…¢andâ…¡groups was significantly lowerthanthose of SiO2 group(P<0.05).At 56th day , HYP content in AAP-treatedâ…¢group was significantly lowerthanthose of SiO2 group(P<0.01).⑸the changes of SOD content:At 14th day,SOD activities in AAP-treated groups was significantly higher than those of SiO2 group(P<0.05) . At 56th day,SOD activities in AAP -treated groupâ…¢was still higher than those of SiO2 group(P<0.05).⑹the changes of MDA conten: At 14th day, MDA content in AAP-treatedâ…¢andâ…¡groups were significantly lower than those of SiO2 group(P<0.05) . At 56th day,MDA content in AAP-treated groupâ…¢was still significantly lower than those of SiO2 group(P<0.01).⑺the changes of NO conten:At 14th day,NO content in AAP-treated groupâ…¢was lower than those of SiO2 group(P<0.05). At 56th day,NO content in AAP-treatedâ…¢group were lower than those of SiO2 group(P<0.01). Conclusion AAP can inhibit synthesization of lung collagen and ameliorate the silica-induced pulmonary fibrosis by increasing the activities of SOD ,inhibitting MDA and NO content and alleviating the damage of peroxidation to the lungs. |