首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Impaired activities of cyclic adenosine monophosphate-responsive element binding protein, protein kinase A and calcium-independent phospholipase A2 are involved in deteriorated regeneration of cirrhotic liver after partial hepatectomy in rats.
【24h】

Impaired activities of cyclic adenosine monophosphate-responsive element binding protein, protein kinase A and calcium-independent phospholipase A2 are involved in deteriorated regeneration of cirrhotic liver after partial hepatectomy in rats.

机译:环肝腺苷单磷酸反应元件结合蛋白,蛋白激酶A和非钙依赖性磷脂酶A2的活性受损,参与了大鼠部分肝切除术后肝硬化肝的再生能力下降。

获取原文
获取原文并翻译 | 示例
           

摘要

Aims: This study is to elucidate whether cyclic adenosine monophosphate (cAMP)-mediated signal is involved in lower regenerative potential of cirrhotic liver. Methods: Hepatic cAMP concentration, activities of protein kinase A (PKA), c-AMP responsive element binding protein (CREB) and Ca(2+) -independent phospholipase A(2) (iPLA2) and regeneration rate were compared between rats with thioacetamide-induced cirrhotic and normal livers after two-third hepatectomy. Results: The liver regeneration estimated by the rates of [(3) H]-thymidine incorporation and staining of proliferating cell nuclear antigen was significantly lower in the cirrhotic group. CREB, PKA and iPLA2 activities, assessed by western blots and electromobility shift assay, were significantly impaired after hepatectomy in the cirrhosis group. PKA and iPLA2 silencing by siRNA transfection significantly inhibited CREB activity and cell growth in transformed hepatocytes in vitro. Conclusions: CREB dysfunction, mediated by PKA and iPLA2 suppression, may be involved in the deteriorated liver regeneration in the cirrhotic rats.
机译:目的:本研究旨在阐明环磷酸腺苷(cAMP)介导的信号是否与肝硬化肝的较低再生潜力有关。方法:比较了硫代乙酰胺大鼠的肝cAMP浓度,蛋白激酶A(PKA)活性,c-AMP反应元件结合蛋白(CREB)和Ca(2+)非依赖性磷脂酶A(2)(iPLA2)的再生速率。三分之二的肝切除术后引起的肝硬化和正常肝。结果:在肝硬化组中,通过[(3 H)-胸苷掺入率和增殖细胞核抗原染色估计的肝再生显着降低。肝硬化组肝切除术后,通过western印迹和电动迁移率分析评估的CREB,PKA和iPLA2活性显着受损。 siRNA转染使PKA和iPLA2沉默显着抑制了体外转化肝细胞的CREB活性和细胞生长。结论:PKA和iPLA2抑制介导的CREB功能异常可能与肝硬化大鼠肝脏再生能力下降有关。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号