Ten groups of 12 Wistar rats (6 controls and 6 treated) received an intramuscular (i.m.) injection of 100 μl of 0.05 M phosphate-buffered saline (PBS), pH 7.4, or 100 μg of venom/100 μl, respectively, in the right gastrocnemius muscle. This amount of venom was chosen based on preliminary experiments with 50, 100 and 150 μg of venom which showed that 100 μg of venom/100 μL gave the best response. After injection, the rats were maintained in cages (five/cage) at 22 °C, on a 12 h light–dark cycle, with food and water ad libitum. CYC202 clinical trial At various

times after treatment (1, 3, 6 or 18 h, or 1, 2, 3, 7, 14 or 21 days) the rats were anesthetized with halothane (Cristália, Itapira, SP) and killed by cervical dislocation and the injected muscle was immediately dissected. Samples were taken from the medial aspect around the injection site and processed for histological and immunohistochemical analysis. Muscle samples were fixed in 4% paraformaldehyde and embedded in paraffin. Serial 5 μm thick cross-sections and longitudinal sections were mounted on silanized glass this website slides. One section from each sectioning plane (cross-section or longitudinal section) per animal was stained by hematoxylin and eosin (H&E) or Masson’s trichrome (MT) (n = 6/time interval/staining method), the latter being used to stain connective

tissue. To detect acute changes in muscle fiber size, the small diameter (to avoid error if fibers were not perfectly cross-sectioned) of muscle cells in the damaged area was measured 1 h post-venom and compared with the corresponding time-matched PBS controls. The damaged area was defined as that presenting hemorrhage, edema and/or altered muscle fibers. For each rat, the small diameter of 200 fibers (total of 1200 fibers per group since each group contained six rats) was measured using a photomicroscope (BX51, Olympus, Japan), a 200× magnification, and Image

Pro-Plus software. To evaluate regeneration, the small diameter of regenerated fibers with centrally-located nuclei (n = 205 fibers) at 21 days post-venom was compared with that of apparently normal fibers (peripherally-located nuclei; n = 205) in the same rats (n = 6). To ensure that the fibers with peripherally-located (-)-p-Bromotetramisole Oxalate nuclei in envenomed muscles were indeed normal measurements were also taken of 205 fibers in control rats (21 days after the injection of PBS). Sections (5 μm thick) of gastrocnemius muscle from each interval (1, 3, 6 or 18 h, or 1, 2, 3, 7, 14 or 21 days) were deparaffinized with xylene and hydrated with decreasing concentrations of ethanol and distilled water. Endogenous peroxidase activity was blocked by immersing the slides in a 3% H2O2 solution. Antigen retrieval was done by incubating the sections with 10 mM sodium citrate buffer, pH 6.0, in a steamer (95–99 °C) for 30 min. The slides were subsequently incubated with reconstituted milk powder to block nonspecific antigenic sites.