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急性林丹处理对离体灌注大鼠肝脏中库普弗细胞功能的剂量依赖性影响。

Dose-dependent effects of acute lindane treatment on Kupffer cell function assessed in the isolated perfused rat liver.

作者信息

Videla L A, Troncoso P, Arisi A C, Junqueira V B

机构信息

Departamento de Bioquímica, Facultad de Medicina, Universidad de Chile, Santiago, Chile.

出版信息

Xenobiotica. 1997 Jul;27(7):747-57. doi: 10.1080/004982597240325.

Abstract
  1. Twenty-four hours after lindane exposure (5-60 mg/kg) a dose-dependent increase in the serum and hepatic levels of the insecticide was observed. Both the basal rate of O2 consumption and the sinusoidal efflux of lactate dehydrogenase (LDH) by the perfused rat liver was enhanced after the administration of 20-60 mg lindane/kg. 2. The administration of low doses of lindane (5-20 mg/kg) increased carbon uptake and the carbon-induced O2 consumption by the perfused liver, effects that were abolished by pretreatment with the Kupffer cell inactivator gadolinium chloride (GdCl3). These parameters were not modified at the higher doses of lindane used (40-60 mg/kg). 3. In the dose range of 20-60 mg lindane/kg, carbon infusion led to a further increase in liver LDH efflux over values found in its absence, an effect that was markedly diminished by GdCl3 in rat treated with 20 mg lindane/kg, being unaltered by GdCl3 in animals given 60 mg/kg. 4. It is concluded that lindane induces a dose-dependent biphasic effect on Kupffer cell function, which could be conditioned by differential membrane perturbation actions of the insecticide that progressively accumulates in the liver, thus altering receptor-mediated and enzymatic processes related to colloidal carbon phagocytosis. Increased Kupffer cell function at low doses of lindane leads to enhanced liver injury. However, this feature of lindane intoxication at higher doses (60 mg/kg) is independent of Kupffer cell activity and seems to be determined by an oxidative stress mechanism induced at the parenchymal cell level.
摘要
  1. 接触林丹(5 - 60毫克/千克)24小时后,观察到血清和肝脏中该杀虫剂水平呈剂量依赖性增加。给予20 - 60毫克林丹/千克后,灌注大鼠肝脏的基础耗氧率和乳酸脱氢酶(LDH)的窦状隙流出量均增加。2. 给予低剂量林丹(5 - 20毫克/千克)可增加灌注肝脏的碳摄取和碳诱导的耗氧量,这些效应可被库普弗细胞灭活剂氯化钆(GdCl3)预处理消除。在使用的较高剂量林丹(40 - 60毫克/千克)下,这些参数未发生改变。3. 在20 - 60毫克林丹/千克的剂量范围内,输注碳导致肝脏LDH流出量比未输注时进一步增加,在用20毫克林丹/千克处理的大鼠中,GdCl3可显著减弱这种效应,而在给予60毫克/千克的动物中,GdCl3对其无影响。4. 得出结论,林丹对库普弗细胞功能诱导出剂量依赖性双相效应,这可能由该杀虫剂在肝脏中逐渐积累的不同膜扰动作用所决定,从而改变与胶体碳吞噬相关的受体介导和酶促过程。低剂量林丹时库普弗细胞功能增强导致肝脏损伤加剧。然而,林丹高剂量(60毫克/千克)中毒的这一特征与库普弗细胞活性无关,似乎由实质细胞水平诱导的氧化应激机制所决定。

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