Test slides were scored only when the internal controls showed clearly positive or negative results (Greggio et al., 2009). One hundred cells (50 cells from each of two replicate slides of each organ) were selected and analyzed for DNA migration. When selecting the cells, cells around the edges or air bubbles were excluded (Azqueta et al., 2009). The cells were scored selleck compound visually into five classes according to tail length: class 0: undamaged, without

a tail; class 1: with a tail shorter than the diameter of the head (nucleus); class 2: with a tail length 1–2 times the diameter of the head; class 3: with a tail longer than 2 times the diameter of the head; and class 4: comets with no heads. International guidelines and recommendations for the comet assay consider visual scoring of the comets to be a well-validated evaluation method (Burlinson et al., 2007). The genotoxic effects were estimated based on two different parameters: damage index (DI) and damage frequency (DF). The damage index ranged from 0 (completely Metformin undamaged: 100 cells × 0) to 400 (with maximum damage: 100 cells × 4). The damage frequency (%) was calculated based on the number of cells with tails compared to the number of cells with no tails. Levels of Endo III and Fpg-sensitive sites were calculated from the DI score obtained with enzyme treatment minus the score without enzyme treatment (buffered). The vehicle was used as a negative control, and treatment

with 4 × 10−5 M MMS for 1 h was

used as a positive control. Statistical analyses were performed using GraphPad Prism 5.0 (GraphPad Software Inc., San Diego, CA, USA). The results were expressed as the means ± standard error (SE). All biochemical and coagulation parameters were measured in triplicate. The significant differences between the mean values of two experimental groups were determined using the Student’s t test. When more than two groups were compared, an analysis medroxyprogesterone of variance was used, followed by Bonferroni’s post-hoc test to compare pairs of means. P values less than 0.05 were chosen to establish significance. Between 2 and 6 h after LOBE administration (1 mg/kg, s.c.), the rats presented signs of acute toxicity, including progressive malaise, lethargy, dyspnea, tachycardia, prostration and high sensitivity at the venom injection site. Despite general weakness, the animals showed no clear signs of neuromuscular toxicity, such as muscle trembling, paralysis or convulsions. Most of the envenomed animals displayed hematuria (dark-brown urine at 6–12 h), but no signs of macroscopic skin hemorrhage, petechiae, ecchymosis, suffusions or nasal and eye bleeding were observed. After 48 h, all of the rats had gradually recovered from the clinical symptoms and returned to normal. Until the end of the experiments (96 h), no deaths were registered. The animals in the control group (injected s.c. with PBS solution) exhibited no ill effects.