40 research outputs found
N-acetylcysteine improves morphologic and functional aspects of ovarian grafts in rats
Liver microcirculation after selective denervation
Microcirculatory disturbances have been related to a decrease in survival after liver transplant. Because innervation is involved in liver hemodynamics regulation, we decided to evaluate microcirculatory hepatic perfusion. Thirty rats were divided into three groups: denervated (DG), hepatic microsurgical denervation; manipulated (MG), hepatic manipulation; control (CG), laparotomy. Hepatic microcirculation was assessed in the median lobe using laser Doppler flowmetry in the following moments: T-0, after laparotomy and T-1, after denervation; and in the following moments after derevation: T-2, 10 minutes, T-3, 20 minutes, T-4, 30 minutes, T-5, 1 hour, T-6, 1.5 hours, and T-7, 2 hours for DG, and in same moments for MG and CG. DG showed a decrease in hepatic perfusion for 20 minutes after denervation, different from MG and CG. After that, there was recovery in hepatic perfusion in MG and DG (Kruskal-Wallis and Friedman tests). Therefore, denervation and manipulation alter hepatic microcirculation, but denervation promotes a more severe decrease than manipulation. (C) 2001 Willey-Liss, Inc.Universidade Federal de São Paulo, Escola Paulista Med, Dept Surg, Operat Tech & Expt Surg Div, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Surg, Operat Tech & Expt Surg Div, BR-04023062 São Paulo, BrazilWeb of Scienc
Bile duct exclusion from selective vascular inflow occlusion in rat liver: Role of ischemic preconditioning and N-acetylcysteine on hepatic reperfusion injury
Aim. To study the effects of N-acetyleysteine and ischemic preconditioning on the portal triad clamping compared to arterial and portal clamping alone.Methods. Eighty EPM 1-Wistar rats were randomized into two groups, depending on inclusion (Group 1) or not (Group 2) of the bile duct in the hepatic vascular pedicle occlusion. Each group was divided into four subgroups as follows. IR 1: 20 minutes after celiotomy, the pedicle containing vascular elements and bile duct to the left lateral and median liver lobes was occluded for 40 minutes, followed by 30 minutes of reperfusion. IPC 1: after 10 minutes of ischemia and 10 minutes of reperfusion, the ischemic preconditioning period, the rats were submitted to the same procedure described for IR 1 Group. NAC 1: the rats received N-acetylcysteine (150 mg/kg) 15 minutes before 40 minutes of ischemia and 5 minutes before 30 minutes of reperfusion. SHAM 1: the hepatic pedicle for the lateral and median liver lobes was dissected after 20 minutes, the bile duct alone was clamped for 40 minutes, and released for an additional 30 minutes. in the IR 2, IPC 2, and NAC 2 groups, ischemia was achieved with an exclusive vascular occlusion. SHAM 2: dissection and observation for 90 minutes. the blood was sampled for liver enzyme levels. Statistical analysis was done (P <= .05).Results. Hepatic IR injury was less severe for animals from the classic portal triad clamping (group 1), with regard to AST (IR 1 Group 766 vs IR 2 Group 1380 U/L) and ALT (IR 1 Group 840 vs IR 2 Group 1576 U/L); IPC, but not NAC administration, was able to protect the liver from IR injury for animals from the classic portal triad clamping group, with regard to AST (IPC 1. Group 421 vs NAC 1 Group 1131 U/L) and ALT (IPC 1 Group 315 vs NAC 1 Group 1.085 U/L).Conclusions. IPC protects the liver from IR injury; classic portal triad clamping results in a less severe hepatic IR injury when compared to bile duct exclusion.Universidade Federal de São Paulo, São Paulo, BrazilFed Univ Goias, Goiania, Go, BrazilUniversidade Federal de São Paulo, EPM, São Paulo, BrazilWeb of Scienc
The role of the small bowel as a barrier for bacterial septic shock
Universidade Federal de São Paulo, Dept Microbiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pediat, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pediat, São Paulo, BrazilWeb of Scienc
