Figures & data
Figure 2. UV-HPLC at 254 nm of Equisetum myriochaetum: (1) kaempferol-3-O-sophoroside and (2) kaempferol-3,7-di-O-β-glucoside.
![Figure 2. UV-HPLC at 254 nm of Equisetum myriochaetum: (1) kaempferol-3-O-sophoroside and (2) kaempferol-3,7-di-O-β-glucoside.](/cms/asset/9f110aa8-9019-4a35-8c59-64451b60de0c/iphb_a_527992_f0002_b.gif)
Table 1. Frequency and number of spots/wing obtained after chronic exposure of trans-heterozygous larvae of Drosophila melanogaster to different concentrations of the phytoextracts tested.
Table 2. Fly spot data obtained after chronic exposure of trans-heterozygous larvae of Drosophila melanogaster to different concentrations of hydrogen peroxide.
Table 3. Effect of the phytoextracts on the genotoxicity of hydrogen peroxide in the pretreatment protocol.
Figure 3. Catalase-specific activity in third instar Drosophila melanogaster larvae treated or not with 0.2 M hydrogen peroxide. Data are expressed as nanomoles of oxidized hydrogen peroxide/min/mg of total protein. (A) Standard cross; (B) high-bioactivation cross. *P < 0.05.
![Figure 3. Catalase-specific activity in third instar Drosophila melanogaster larvae treated or not with 0.2 M hydrogen peroxide. Data are expressed as nanomoles of oxidized hydrogen peroxide/min/mg of total protein. (A) Standard cross; (B) high-bioactivation cross. *P < 0.05.](/cms/asset/9804b230-0a27-4eae-a90f-45f5ac805f99/iphb_a_527992_f0003_b.gif)