Abstract OBJECTIVE: To investigate the effect of recombinant human erythropoietin (rhEpo) on hyperoxia induced lung injury in premature rats. METHODS: Three dayold premature rats were randomly assigned to four groups: Ⅰ. the room air group, Ⅱ. the hyperoxia group, Ⅲ. the hyperoxia+rhEpo group, Ⅳ. the room air+rhEpo group. Group Ⅰ and Ⅲ rats were exposed to 90% O2. Group Ⅲ and Ⅳ rats received rhEpo (800 U/kg) subcutaneously every other day. After 3 days or 7 days of exposure, the contents of glutathione (GSH), total protein, malondialdehyde (MDA) and nonheme iron in the bronchoalveolar lavage fluid (BALF) and the ratio of lung wet weight/dry weight (W/D), and lung morphometry were examined in all groups. RESULTS: ① After 3 days, Group Ⅱ rats showed an increase of MDA content compared with Group Ⅰ rats ［(1.39±0.60) nmol/ml vs (0.35±0.22) nmol/ml，P<0.01］, and presence of hyperaemia, red cell extravasation and inflammatory infiltration. After 7 days of exposure, the contents of nonheme iron, total protein and MDA increased in Group Ⅱ rats compared with Group Ⅰ rats ［(109.31±7.86) μg/dl vs (94.95±10.83) μg/dl, (1.53±0.39) nmol/ml vs (0.30±0.13) nmol/ml，(0.47±0.02) g/L vs (0.25±0.04) g/L, respectively］, P<0.01. And the ration of lung W/D also increased ［(5.54±0.41) vs (5.00±0.15)］，P<0.05, and pathologic changes were more severe than those after 3 days of exposure. ② After 3 days of exposure, compared with Group Ⅱ rats, MDA content ［(0.69±0.19) nmol/ml］ in Group Ⅲ rats decreased significantly (P<0.01), and the changes of acute lung injury were also alleviated. After 7 days of exposure, the contents of MDA ［(0.80±0.24) nmol/ml］, total protein ［(0.36±0.02) g/L］, nonheme iron ［(99.60±8.21) μg/dl］ and lung W/D (5.08±0.21) also decreased in Group Ⅲ rats compared with Group Ⅱ rats (P<0.01 or 0.05). GSH contents increased in Group Ⅲ rats both after 3 days and 7 days of exposure ［(130.85±7.62) mg/L and (136.69±5.90) mg/L］ compared with those in Group Ⅱ rats ［(106.86±9.87) mg/L, (122.19±10.41) mg/L］(both P<0.01), and pathologic changes in Group Ⅲ rats were alleviated more than those in Group Ⅱ rats. CONCLUSIONS: Exposure to 90% O2 for 3 days and 7 days result in acute lung injury in pretmature rats. Treatment with rhEpo alleviates hyperoxic lung injury in premature rats.
QUAN Yu-Feng,CHANG Li-Wen,ZHANG Guo-Feng et al. Effect of Recombinant Human Erythropoietin on Hyperoxia Induced Lung Injury in Premature Rats[J]. 中国当代儿科杂志, 2001, 3(5): 525-528.
QUAN Yu-Feng,CHANG Li-Wen,ZHANG Guo-Feng et al. Effect of Recombinant Human Erythropoietin on Hyperoxia Induced Lung Injury in Premature Rats[J]. CJCP, 2001, 3(5): 525-528.
