We evaluated the in vivo myotoxicity of Bothrops snake venoms using two different protocols. First we assessed the activity of creatine kinase (CK) in plasma, which increases in cases of muscle damage. Mice received perimuscular injections of venom, as described above. Two hours after the injection of venom alone or associated with treatments, the animals were lightly anesthetized and ROCK inhibitor blood was collected by orbital puncture. The determination of plasma CK activity was performed as previously described ( Melo and Suarez-Kurtz, 1988b; Melo et al., 1993 and Melo et al., 1994), and

expressed as units per liter of plasma (U/L). We also determined the EDL muscle CK content in the same groups of mice at 24 and 72 h after the injections, which is expected to decrease in cases of muscle damage. Animals were sacrificed under anesthesia, then the EDL muscles were removed, weighed, minced and homogenized in 2 mL PSS + 0.1% albumin and the CK content was determined in the homogenate as described previously ( Melo and Ownby, 1996; Tomaz et al., 2008). The results

were expressed as units per gram see more of muscle tissue (U/g). Inflammation was assessed by multiple parameters. The local edema induced by the venom, and the protection by the treatments, were evaluated using a caliper rule. The diameters of mice legs were measured before and 1 h after the perimuscular venom injections (as described above) and the results are shown as mm of increase in the leg diameter click here (Melo et al., 2010). Blood was collected by orbital puncture under ether anesthesia 24 h after the injections, and treated with Turk’s solution (19:1 v/v) for leukocyte count in a Neubauer chamber. The results are shown as leukocytes per mm3 (×103 cells/mm3). The same animals were

killed under anesthesia and the EDL muscles were removed, weighed, minced and homogenized in 2.0 mL PSS and then centrifuged at 20,000 rpm. We then removed 1.8 mL of the supernatant, resuspended the cell pellet and treated a 20 μL sample with 380 μL of Turk’s solution. The leukocyte count was performed in Neubauer chamber and the results expressed in leukocytes per gram of muscle tissue (×106 cells/g). To determine the myeloperoxidase (MPO) activity in the muscles, EDL muscles were removed, weighed, minced and homogenized in 1.0 mL of 0.5% hexadecyltrimethyl-ammonium bromide (HTAB) in potassium phosphate buffer 50 mM, pH 6.0 (Bradley et al., 1982). After centrifugation at 10,000 rpm for 5 min, 100 μL samples of the supernatant were mixed with potassium phosphate buffer 50 mM containing 1.0 mM O-dianisidine dihydrochloride and 0.001% H2O2. Absorbance was measured at 460 nm taking 4 readings at 60 s intervals. Each MPO unit activity was defined as that degrading 1 μmol of H2O2 per minute at 25 °C and considering that 1 μmol H2O2 gives a change in absorbance of 1.13 × 10−2 nm min−1 (Posadas et al., 2004). The results were expressed as units per gram of muscle tissue (U/g).