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. 2017 Aug 3;8(43):73529–73546. doi: 10.18632/oncotarget.19867

Figure 4. As2O3 prevented the progression of arthritis in CIA mice.

Figure 4

A. Representative photography of the hind limb from mice were shown. There was no obvious remission of arthritis in CIA control mice on the 1st(I), 7th(II) and 14th(III) day after drug treatment, while clinical symptoms of CIA mice treated with As2O3 at dose of 5.0 mg/kg/day had been improved significantly through the 1st(IV), 7th(V) and 14th(VI) days after drug administration. B. Arthritis scores of the mice were evaluated from 19th day after primary immunization to 40th day. Mice with CIA were administrated As2O3 and MTX intraperitoneally from 26th day to 39th day after 1st immunization. The arthritis scores of normal group were nearly 0 on each test day (data not shown). CIA mice treated with As2O3 at doses of 2.0 mg/kg/day (n = 6), 5.0 mg/kg/day (n = 6) and MTX 1.5mg/kg/week (n = 6) showed significant improvement on arthritis score along with the treatment compared to the CIA control group (n = 6, *p < 0.05, **p < 0.01). Data are expressed as the mean ± S.E.M, Con = control = CIA control group. MTX = methotrexate.