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首页> 外文期刊>Journal of Surgical Research: Clinical and Laboratory Investigation >Phenobarbital in comparison with carbon tetrachloride and phenobarbital-induced cirrhosis in rat liver regeneration.
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Phenobarbital in comparison with carbon tetrachloride and phenobarbital-induced cirrhosis in rat liver regeneration.

机译:苯巴比妥与四氯化碳和苯巴比妥所致肝硬化的大鼠肝脏再生比较。

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BACKGROUND: The simultaneous administration of carbon tetrachloride (CCl4) and phenobarbital in the rat produces one of the most common experimental models of liver cirrhosis. As phenobarbital also has a hepatotrophic effect, its role in liver regeneration following partial hepatectomy (HTX) is not elucidated. PURPOSE: To examine the effect of long-term administration of phenobarbital in liver regeneration after HTX with regard to CCl4-induced cirrhotic rat model. Materials and Methods. The liver regeneration following HTX in phenobarbital-treated rats (PB rats) was compared to that seen in cirrhotic rats (LC rats), induced by oral gavage of CCl4 and phenobarbital, and normal rats. The effect of the withdrawal of phenobarbital was also examined. Liver regeneration was estimated 24 h after the HTX by measuring the liver weight, the DNA content in the liver, and [3H]thymidine incorporation into the DNA. RESULTS: Treatment with CCl4 and phenobarbital caused liver deformity, and the highest percentage of liver weight regeneration was seen in LC rats with this deformity, even though [3H]thymidine incorporation into the DNA was impaired in this group. Phenobarbital had a hepatotrophic effect, but its withdrawal caused a decrease in liver mass and cessation of body weight gain. The change in the DNA content 24 h after HTX was negative in PB rats. CONCLUSIONS: Liver regeneration could not be estimated using liver or body weight in the PB or LC rat model. [3H]Thymidine incorporation into the DNA was reliable indicator of liver regeneration in the different liver states during the early stage after HTX. Although the DNA content with respect to total liver mass was obscured due to liver inflation in PB rats, [3H]thymidine incorporation into the DNA between PB rats and normal rats was similar. Copyright 1999 Academic Press.
机译:背景:在大鼠中同时施用四氯化碳(CCl4)和苯巴比妥可产生最常见的肝硬化实验模型之一。由于苯巴比妥也具有肝营养作用,因此尚未阐明其在部分肝切除术(HTX)后在肝再生中的作用。目的:就CCl4诱导的肝硬化大鼠模型,探讨长期服用苯巴比妥对HTX后肝再生的影响。材料和方法。将经苯巴比妥治疗的大鼠(PB大鼠)HTX后的肝脏再生与肝硬化大鼠(LC大鼠)中因CCl4和苯巴比妥的口服灌胃诱导的肝再生以及正常大鼠的肝再生进行了比较。还检查了苯巴比妥退出的效果。通过测量肝脏重量,肝脏中的DNA含量以及[3H]胸苷掺入DNA中,估计HTX后24小时的肝脏再生。结果:使用CCl4和苯巴比妥治疗可导致肝脏畸形,即使该组DNA中[3H]胸苷的掺入受损,在患有这种畸形的LC大鼠中,肝脏重量再生的百分比最高。苯巴比妥具有保肝作用,但停药会导致肝脏质量下降和体重增加停止。 HTX后24小时,PB大鼠的DNA含量变化为阴性。结论:在PB或LC大鼠模型中,无法使用肝脏或体重估算肝脏再生。 [3H]胸腺嘧啶核苷掺入DNA是HTX后早期不同肝脏状态下肝脏再生的可靠指标。尽管由于PB大鼠的肝脏充血,相对于总肝脏质量的DNA含量被遮盖了,但是[3H]胸苷掺入PB大鼠和正常大鼠之间的DNA相似。版权所有1999,学术出版社。

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