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1.
Acta cir. bras ; 31(6): 389-395, tab, graf
Article in English | LILACS | ID: lil-785020

ABSTRACT

ABSTRACT PURPOSE: To investigate the potential efficacy of beractant (Survanta(r)) and Seprafilm(r) on the prevention of postoperative adhesions. METHODS: Forty Wistar-albino female rats were used. The rats were randomly allocated into four groups of 10 rats each as control group (CG), beractant group (BG), Seprafilm(r) group (SG), and combined group (COG). All rats underwent cecal abrasion via midline laparotomy. Before abdominal closure, isotonic saline, beractant, Seprafilm, and combined agents were intraperitoneally administered. Adhesions were classified macroscopically with Canbaz Scoring System on postoperative day 10. Ceacum was resected for histopathological assessment. RESULTS: Macroscopic adhesion scores were significantly lower in BG, SG, and COG than CG (p<0.05); (45%, 15%, 25%, and 15%; respectively). Histopathological assessment revealed a reduced inflammation and fibrosis score in the study groups than CG (p<0.05). In BG, adhesion development, inflammation and fibrosis scores were lower than SG; however, it was not statistically significant. CONCLUSIONS: Intra-abdominal application of beractant is significantly effective for the prevention of adhesion formation with no adverse effect by covering the whole peritoneal mesothelium with excellent gliding properties in a rat model. The combination of both agents is also effective in reducing adhesion formation, however, not superior to single beractant application.


Subject(s)
Animals , Female , Biological Products/pharmacology , Cecal Diseases/prevention & control , Cecum/drug effects , Hyaluronic Acid/pharmacology , Peritoneum/drug effects , Peritoneum/pathology , Postoperative Care/instrumentation , Fibrosis , Random Allocation , Cecum/surgery , Cecum/pathology , Tissue Adhesions/pathology , Tissue Adhesions/prevention & control , Rats, Wistar , Models, Animal , Drug Therapy, Combination/methods , Inflammation/pathology , Inflammation/prevention & control
2.
Clinics ; 69(11): 763-769, 11/2014. tab, graf
Article in English | LILACS | ID: lil-731108

ABSTRACT

OBJECTIVES: Vardenafil enhances dilatation of vascular smooth muscle and inhibits platelet aggregation. The purpose of this study was to evaluate the clinical effects of vardenafil and pentoxifylline administration in an experimental model of ischemic colitis. METHODS: Forty female Wistar albino rats weighing 250-300 g were randomized into five experimental groups (each with n = 8) as follows:1) a sham group subjected to a sham surgical procedure and administered only tap water; 2) a control group subjected to a standardized surgical procedure to induce ischemic colitis and administered only tap water; 3) and 4) treatment groups subjected to surgical induction of ischemic colitis followed by the postoperative administration of 5 mg/kg or 10 mg/kg vardenafil, respectively; and 5) a treatment group subjected to surgical induction of ischemic colitis followed by postoperative administration of pentoxifylline at 50 mg/kg/day per day as a single dose for a 3-day period. All animals were sacrificed at 72 h post-surgery and subjected to relaparotomy. We scored the macroscopically visible damage, measured the ischemic area and scored histopathology to determine the severity of ischemia. Tissue malondialdehyde levels were also quantified. RESULTS: The mean Gomella ischemic areas were 63.3 mm2 in the control group; 3.4 and 9.6 mm2 in the vardenafil 5 and vardenafil 10 groups, respectively; and 3.4 mm2 in the pentoxifylline group (p = 0.0001). The mean malondialdehyde values were 63.7 nmol/g in the control group; 25.3 and 25.6 nmol/g in the vardenafil 5 and vardenafil 10 groups, respectively; and 22.8 nmol/g in the pentoxifylline group (p = 0.0001). CONCLUSION: Our findings indicate that vardenafil and pentoxifylline are effective treatment options in an animal model of ischemic colitis. The positive clinical effects produced by these drugs are likely due to their influence on the hemodynamics associated ...


Subject(s)
Animals , Female , Colitis, Ischemic/drug therapy , Imidazoles/administration & dosage , Pentoxifylline/administration & dosage , /administration & dosage , Piperazines/administration & dosage , Colitis, Ischemic/pathology , Colitis, Ischemic/surgery , Colon/pathology , Colon/surgery , Disease Models, Animal , Hemodynamics/drug effects , Malondialdehyde/analysis , Random Allocation , Rats, Wistar , Reproducibility of Results , Sulfones/administration & dosage , Time Factors , Treatment Outcome , Triazines/administration & dosage
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