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. 2015 Oct-Dec;38(4):490–498. doi: 10.1590/S1415-475738420150046

Table 2. Tail Intensity (% tail DNA) and cell viability (expressed as % in relation to saline solution group) in cells of kidney and peripheral blood after subacute treatment with CMN SD, unmodified CMN, cDDP and their associations, analyzed in the comet assay.

Treatments % tail DNA Cell viability (%)
Kidney Peripheral blood Kidney Peripheral blood
Saline solution 7.4 ± 4.0 4.4 ± 2.1 100.0 ± 0.0 100.0 ± 0.0
GLA 8.3 ± 2.9 2.6 ± 0.7 88.5 ± 1.9 98.8 ± 0.7
CMN SD 5 9.4 ± 2.8 4.7 ± 1.6 91.2 ± 2.4 99.2 ± 0.7
CMN SD 25 6.7 ± 1.7 4.8 ± 0.6 88.0 ± 2.6 98.7 ± 0.5
CMN SD 50 7.5 ± 3.0 2.1 ± 1.1 88.5 ± 3.3 99.0 ± 0.6
CMN 50 5.5 ± 2.8 3.2 ± 0.9 89.0 ± 2.3 98.7 ± 0.5
cDDP 3.4 ± 1.1* 2.5 ± 0.4 89.7 ± 1.7 99.2 ± 0.7
GLA + cDDP 3.8 ± 0.7* 2.2 ± 0.8 86.5 ± 3.1 98.8 ± 0.7
CMN SD 5 + cDDP 5.0 ± 1.1 3.0 ± 1.7 90.5 ± 2.5 99.8 ± 0.7
CMN SD 25 + cDDP 6.4 ± 1.1 4.4 ± 1.2 87.3 ± 3.6 98.5 ± 1.2
CMN SD 50 + cDDP 5.7 ± 1.1 3.3 ± 1.5 85.5 ± 4.4 98.5 ± 1.4
CMN 50 + cDDP 4.0 ± 0.8 2.1 ± 0.6 88.5 ± 2.2 99.2 ± 0.7

Saline solution or cDDP was administered intraperitoneally 30 min after the last gavage of CMN SD or unmodified CMN. %: percentage; cDDP: cisplatin (6 mg/kg b.w.); CMN: curcumin; GLA: gelucire®50-13/aerosil®; SD: solid dispersion. The results represent the mean ± standard deviation for each group (six animals/group).

*

Significantly different from saline solution group, assessed by ANOVA and Tukey’s post hoc test (p < 0.05).