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Ability of recombinant human endostatin to reduce H22 ascites in mice
Cao-Qian-Qian, XIE Wei-Min, TANG Jing, WU Jie, LU Yong-Kui, ZHOU Wen-Xian, WANG Hong-Xue, YI Wei-Li, ZHENG Ze-Bin
2012, 4 (2):
153-157.
doi: 10.3969/j.issn.1674-5671.2012.02.14
Objective To investigate the effect of intraperitoneal endostar administration to treat H22 ascites in mice. Methods A mouse model of ascites was established by inoculating 110 Kunming mice with H22 cells(2×106,i.p. injection).Mice were then di-vided randomly into 5 groups:control (normal saline);low endostar dose(4 mg/kg•day),intermediate endostar dose(8 mg/kg•day), high endostar dose(12 mg/kg•day)and positive control(DDP 0.6 mg/kg•day).After an adjustment period of 24h,the groups were treated from day 1 to day 10 by i.p. injection as indicated above and sacrificed 24h after drug withdrawal.Data were collected on vol-ume of ascitic fluid,metastases of abdominal organs and lungs and survival time.Peritoneal membrane permeability was assessed us-ing Evan blue staining. Results Intermediate and high doses of endostar significantly inhibited the production of ascites in H22 as-citesbearing mice,reduced the frequency of metastases in the abdominal viscera and lungs,and lengthened average survival time. Conclusion Intraperitoneal administration of endostar can reduce ascites in H22 ascites-bearing mice.
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