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Effect of procainhydrochloride on phospholipase A2 catalytic activity in sodium taurocholate-induced acute experimental pancreatitis in rats.

机译:盐酸普鲁卡因对牛磺胆酸钠引起的大鼠急性实验性胰腺炎中磷脂酶A2催化活性的影响。

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BACKGROUND: In human acute pancreatitis (AP) the local anaesthetic procainhydrochloride (procain-HCl) is given intravenously for pain treatment. Procain has been shown to inhibit catalytic activity of pancreatic (group I) phospholipase A2 (PLA2) and non-pancreatic (group II) PLA2. Both enzymes are important mediators for the local and systemic inflammatory process in AP. To determine the effect of procain, we examined serum and tissue levels of both types of PLA2 activity in the experimental rodent taurocholate model of AP. METHODS: In 60 rats, severe pancreatitis was induced by taurocholate. Forty rats were treated with procain-HCl intravenously at a dosage of 2 mg/kg body weight/h either at or 1 h after induction of pancreatitis. Twenty rats served as controls. We measured catalytic activities of group I and group II PLA2 in serum and tissue samples of lung and pancreas. RESULTS: Serum group II PLA2 catalytic activity was significantly reduced 3 and 6 h after AP induction in rats treated with procain-HCl (p < 0.001) in both treatment groups. In pancreatic and lung tissue, group II PLA2 catalytic activity was significantly reduced compared with normal values (p < 0.001). CONCLUSION: Procain-HCl given intravenously either at or 1 h after induction of necrotizing pancreatitis significantly inhibits group II PLA2 catalytic activity in serum and tissues.
机译:背景:在人类急性胰腺炎(AP)中,静脉内使用局部麻醉的普鲁卡因盐酸盐(procain-HCl)进行疼痛治疗。普鲁卡因已显示出抑制胰腺(I组)磷脂酶A2(PLA2)和非胰腺(II组)PLA2的催化活性。两种酶都是AP局部和全身炎症过程的重要介质。为了确定普鲁卡因的作用,我们在AP实验性啮齿动物牛磺胆酸盐模型中检查了这两种PLA2活性的血清和组织水平。方法:60只大鼠中,牛磺胆酸盐可引起严重的胰腺炎。在诱导胰腺炎时或诱导后1小时,以2 mg / kg体重/ h的剂量静脉注射普鲁卡因-HCl治疗40只大鼠。二十只大鼠作为对照。我们在肺和胰腺的血清和组织样本中测量了I组和II组PLA2的催化活性。结果:在两个治疗组中,用普鲁卡因-HCl(p <0.001)处理的大鼠在诱导AP后3和6 h,血清II组PLA2的催化活性显着降低。在胰腺和肺组织中,与正常值相比,II组PLA2的催化活性显着降低(p <0.001)。结论:在诱导坏死性胰腺炎后1小时或之后1小时静脉给予普鲁卡因HCl可显着抑制血清和组织中的II组PLA2催化活性。

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