Mandibular Fractures in the Cat A Retrospective Study

A retrospective study was made of 75 mandibular fractures in 62 cats. Mandibular fractures comprised 14.5% of all fractures seen in 517 cats. Automobile trauma was the cause of injury in more than 50% of the cases. The mean age of patients was 29.5 months. Symphyseal fractures were most common (73.3%), followed by fractures of the body (16%), condyle (6.7%), and coronoid process (4%). Sixty-seven percent of the fractures were stabilized. Cerclage and interfragmentary wiring were the most common forms of fixation. Antibiotics were administered to 73.6% of the patients. Complications were reported in 24.5% of the cats. Malocclusion and soft tissue infections were the most frequent complications. Complications developed more commonly in cats with multiple or open fractures. Clinical union occurred by an average of 6 weeks (range, 3-12 weeks) for symphyseal fractures, 10 weeks (range, 8-16 weeks) for body fractures, 6 weeks for coronoid fractures, and 6 weeks (range, 4-8 weeks) for condylar fractures.     

Biomechanical Study of Canine Spinal Fracture Fixation Using Pins or Bone Screws With Polymethylmethacrylate

Five configurations of pins or screws interconnected with polymethylmethacrylate (PMMA) were applied to isolated canine lumbar spines (L2 to L5) in which a complete fracture-luxation had been produced at L3 to L4. Twenty-five repaired spines and five intact control spines were subjected to four-point bending and tested once to failure in ventral flexion. The purpose of this study was to determine the effects of pin number, pin angle, and use of 3.5-mm cortical bone screws instead of smooth 3.2-mm diameter pins on rigidity and ultimate strength of spinal fractures repaired by the implant-PMMA fixation technique. Bending moment versus the angular deformation curves were recorded. Rigidity, bending moment at 10° angular deformation, moment at failure, and deformation at failure of each type of fixation were compared using analysis of variance. Spinal segments stabilized with eight pin-PMMA fixation had significantly greater rigidity and strength at failure than four pin-PMMA fixations ( P < .05). Furthermore, spinal segments stabilized with eight pins angled away from the fracture failed at significantly greater bending moment than those with eight pins angled toward the fracture ( P < .05). However, for four-pin fixation, greater strength was achieved by angling pins in the bone toward the fracture site ( P < .05). Screw-PMMA fixations failed by screw bending and were less rigid and weaker at failure than the corresponding configuration of pin-PMMA fixation ( P < .05).     

α‐6 Integrin Expression in Bovine Spermatogonial Cells Purified by Discontinuous Percoll Density Gradient

The study of spermatogonial stem cells (SSCs) provides a model to better understand adult stem cell biology. Besides the biomedical potential to perform studies of infertility in many species, SSCs hold a promising application at animal transgenesis. Because stem cells are thought to be associated with basement membranes, expression of α‐6 integrin has been investigated as a marker of type A spermatogonial cells, which are considered SSCs because of their undifferentiated status and self‐renewal ability. In this manner, the aim of this study was to isolate type A SSCs from adult bulls by a two‐step enzymatic procedure followed by a discontinuous Percoll density gradient purification and verify the expression of α‐6 integrin by flow cytometry and real‐time RT‐PCR before and after Percoll purification. Spermatogonial cells were successfully obtained using the two‐step enzymatic digestion. An average of 1 × 10⁵ viable cells per gram of testis was isolated. However, the discontinuous Percoll did not purify isolated cells regarding α‐6 integrin expression. Flow cytometry analysis demonstrated no differences in the α‐6 integrin expression between cell samples before and after Percoll purification (p = 0.5636). The same was observed in the real‐time PCR analysis (p > 0.05). In addition to α‐6 integrin, the expression of GFRa‐1 and PGP9.5, known bovine SSCs markers, was detected in all samples studied. Considering that Percoll can reduce cell viability, it is possible to conclude that Percoll density gradient is not suitable to purify bovine SSC, according to α‐6 integrin expression.