Analysis of hepatic reserve function after extended hepatectomy and treatment of acute liver failure induced by extended hepatectomy

扩大肝切除术后肝脏储备功能分析及扩大肝切除所致急性肝功能衰竭的治疗

基本信息

  • 批准号:
    16591332
  • 负责人:
  • 金额:
    $ 2.11万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    2004
  • 资助国家:
    日本
  • 起止时间:
    2004 至 2005
  • 项目状态:
    已结题

项目摘要

Extended hepatectomy for advanced biliary cancer may result in acute liver failure even if in patients with normal liver function. Preoperative and postoperative evaluation of hepatic reserve function especially in patients with liver cirrhosis or obstructive jaundice, to prevent postoperative liver failure, is very important.1.The changes of mRNA expression of the organic anion transporters (mrp2, mrp3, bsep, oatp and ntcp) depending on the duration of bile duct ligation have been examined in rats. Blood and liver tisues were obtained during the period from 3 to 28 days after the ligation. The excretion transporters, the mRNA levels of mrp2 and bsep decreased, while those of mrp3 increased from 3 days until 28 days after the ligation. The uptake transporters, ntcp and oatp decreased until 28 days after the ligation. After 7 days ligation of bile duct, external and internal biliary drainage were performed. The expression of mrp2 mRNA levels increased, while those of mrp3 decreased. The … More se changes of mrp2 and mrp3 mRNA expressions were significantly stronger in the internal biliary drainage than the external drainage. These suggest that the internal biliary drainage is useful for hepatic function reserve. We are now examining the expression of these protein levels.2.We evaluated the differences in hepatic reserve function and parameters to predict the liver failure in the early stage after extended hepatectomy in rats. The survival rates of 48 hours after hepatectomy were 50% in 90% hepatectomy and 100% in 70% hepatectomy. 90% hepatectomy is a model for acute liver failure. We determined the bile flow, biliary bile acid excretion and the mRNA levels of organic anion transporters (mrp2, mrp3 and bsep) after 70% or 90% hepatectomy in rats. The bile flow and bile acid excretion both decreased significantly after the 90% hepatectomy. Biliary bile acid excretion and the expression of mrp2 decreased, while the expressions of mrp3 and bsep increased after 90% hepatectomy. In contrast, the expression of mrp2 increased, while the expressions of mrp3 and bsep decreased after 70% hepatectomy. The expressions of mrp2 and mrp3 were differently regulated after 70% and 90% hepatectomy. We suspected that expressions of mrp2 and mrp3 and biliary bile acid excretion and bile flow might be able to predict the liver failure after extended hepatectomy. Less
晚期胆道癌的扩大肝切除术可能导致急性肝功能衰竭,即使在肝功能正常的患者中也是如此。术前、术后评估肝储备功能,特别是对有肝硬变或梗阻性黄疸的患者,对于预防术后肝功能衰竭非常重要。1.观察了大鼠胆管结扎后不同时间有机阴离子转运体(mrp2、mrp3、bsep、oatp和ntcp)mRNA表达的变化。于结扎后3~28d取血和肝组织。排泄转运蛋白mrp2和bsep的表达水平在结扎后3d开始下降,而mrp3的表达在3d至28d逐渐升高。摄取转运体ntcp和oatp在结扎后28d下降。术后7d结扎胆管,行胆道外引流和内引流。Mrp2基因表达水平升高,mrp3基因表达水平降低。The…胆道内引流较外引流mrp2、mrp3基因表达的改变更明显。提示胆道内引流有利于肝功能储备。我们正在检测这些蛋白水平的表达。2.我们评估了肝储备功能和参数的差异,以预测大鼠扩大肝切除术后早期肝功能衰竭。肝切除后48h存活率,90%肝切除组为50%,70%肝切除组为100%。90%肝切除是急性肝功能衰竭的一种模型。我们测定了大鼠70%和90%肝切除后胆汁流量、胆汁酸排泄量和有机阴离子转运体(mrp2、mrp3和bsep)的mRNA水平。90%肝切除后胆汁流量和胆汁酸排泄量均明显减少。90%肝切除后胆汁中胆汁酸排泄量和mrp2表达减少,mrp3和bsep表达增加。相反,70%肝切除后mrp2表达增加,mrp3和bsep表达降低。70%和90%肝切除后,mrp2和mrp3的表达受到不同程度的调节。我们推测mrp2和mrp3的表达以及胆汁中胆汁酸的排泄和胆汁流量可能能够预测扩大肝切除术后的肝功能衰竭。较少

项目成果

期刊论文数量(12)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Risk factors for early death after liver resection in patients with solitary hepatocellular carcinoma
Prognostic benefit of selective portal vein occlusion during hepatic resection for hepatocellular carcinoma
  • DOI:
    10.1016/j.surg.2005.02.008
  • 发表时间:
    2005-06-01
  • 期刊:
  • 影响因子:
    3.8
  • 作者:
    Makino, I;Chijiiwa, K;Kai, M
  • 通讯作者:
    Kai, M
Biliary Lipid Output in the Early Stage of Acute Liver Failure Induced by 90% Hepatectomy in the Rat
胆汁%20脂质%20输出%20in%20the%20早期%20阶段%20of%20急性%20肝脏%20失败%20诱导%20by%2090%%20肝切除%20in%20the%20Rat
Biliary lipids output in the early stage of acute liver failure induced by 90% hepatectomy in the rat
胆道%20脂质%20输出%20in%20the%20早期%20阶段%20of%20急性%20肝脏%20失败%20诱导%20by%2090%%20肝切除%20in%20the%20rat
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KAI Masahiro其他文献

波浪による転動石の鋼製桟橋への衝突の再現実験
滚石因波浪撞击钢墩的再现实验
  • DOI:
  • 发表时间:
    2021
  • 期刊:
  • 影响因子:
    0
  • 作者:
    TSUTSUMI Ayato;YAMAMOTO Atsushi;KAI Masahiro;TAKANO Daiki;TAKAHASHI Hidenori;SAKAKIBARA Junichi;鈴木健太,小口智弘,先名重樹,王欣,永野正行;今井 脩雅・木村 克俊・宮武 誠・山本 泰司・名越 隆雄・阿部 翔太
  • 通讯作者:
    今井 脩雅・木村 克俊・宮武 誠・山本 泰司・名越 隆雄・阿部 翔太
関東地域における浅部深部統合地盤を用いた超高層集合住宅の地震応答評価
关东地区浅层和深层综合土高层公寓的地震反应评价
  • DOI:
  • 发表时间:
    2020
  • 期刊:
  • 影响因子:
    0
  • 作者:
    TSUTSUMI Ayato;YAMAMOTO Atsushi;KAI Masahiro;TAKANO Daiki;TAKAHASHI Hidenori;SAKAKIBARA Junichi;鈴木健太,小口智弘,先名重樹,王欣,永野正行
  • 通讯作者:
    鈴木健太,小口智弘,先名重樹,王欣,永野正行
地表断層を伴う震源モデルを用いた断層近傍における地盤震動特性- 鉛直右横ずれ断層モデルを用いた検討 -
使用带有地表断层的震源模型研究断层附近的地震动特征 - 使用垂直右旋走滑断层模型的研究 -
  • DOI:
  • 发表时间:
    2020
  • 期刊:
  • 影响因子:
    0
  • 作者:
    TSUTSUMI Ayato;YAMAMOTO Atsushi;KAI Masahiro;TAKANO Daiki;TAKAHASHI Hidenori;SAKAKIBARA Junichi;鈴木健太,小口智弘,先名重樹,王欣,永野正行;今井 脩雅・木村 克俊・宮武 誠・山本 泰司・名越 隆雄・阿部 翔太;斉藤日向子,金澤伸一;貴堂峻至,永野正行
  • 通讯作者:
    貴堂峻至,永野正行
WORK PROGRESS CONTROL FOR GROUND IMPROVED BY CHEMICAL GROUTING USING P-WAVE AMPLITUDE ATTENUATION TOMOGRAPHY
利用纵波振幅衰减断层扫描化学灌浆加固地基的施工进度控制
工法規定管理に着目した盛土の初期応力解析
注重工法规范管理的路堤初始应力分析
  • DOI:
  • 发表时间:
    2022
  • 期刊:
  • 影响因子:
    0
  • 作者:
    TSUTSUMI Ayato;YAMAMOTO Atsushi;KAI Masahiro;TAKANO Daiki;TAKAHASHI Hidenori;SAKAKIBARA Junichi;鈴木健太,小口智弘,先名重樹,王欣,永野正行;今井 脩雅・木村 克俊・宮武 誠・山本 泰司・名越 隆雄・阿部 翔太;斉藤日向子,金澤伸一
  • 通讯作者:
    斉藤日向子,金澤伸一

KAI Masahiro的其他文献

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{{ truncateString('KAI Masahiro', 18)}}的其他基金

The functions of a diacylglycerol kinase on cancer cells
二酰甘油激酶对癌细胞的作用
  • 批准号:
    19K05817
  • 财政年份:
    2019
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Study on the epiginetic silencing of diacylglycerol kinase gamma in colorectal cancer
结直肠癌中二酰甘油激酶γ的表观沉默研究
  • 批准号:
    24570166
  • 财政年份:
    2012
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Studies on the NFkB activation via diacylglycerol kinase alpha
二酰甘油激酶α激活NFkB的研究
  • 批准号:
    20570135
  • 财政年份:
    2008
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
The intracellular localization and the physiological properties of type 2 phosphatidic acid phosphatase.
2型磷脂酸磷酸酶的细胞内定位和生理特性。
  • 批准号:
    13670126
  • 财政年份:
    2001
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
The cell surface localization and the physiological roles of type 2 phosphatidic acid phosphatase
2型磷脂酸磷酸酶的细胞表面定位和生理作用
  • 批准号:
    11670131
  • 财政年份:
    1999
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

相似海外基金

Pluripotent stem cell derived hepatocytes for liver failure (PUSH for LIFE)
多能干细胞衍生的肝细胞治疗肝衰竭(PUSH for LIFE)
  • 批准号:
    MR/Z503940/1
  • 财政年份:
    2024
  • 资助金额:
    $ 2.11万
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    Research Grant
Senescent hepatocytes mediate reprogramming of immune cells in acute liver failure
衰老肝细胞介导急性肝衰竭中免疫细胞的重编程
  • 批准号:
    10679938
  • 财政年份:
    2023
  • 资助金额:
    $ 2.11万
  • 项目类别:
I-Corps: Medical device to treat liver failure
I-Corps:治疗肝衰竭的医疗设备
  • 批准号:
    2348688
  • 财政年份:
    2023
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Standard Grant
Development of a Novel Liver Failure Therapy Based on Improvement of Energy Status of Hepatocytes by Oxygenated Perfusion
开发基于氧合灌注改善肝细胞能量状态的新型肝衰竭疗法
  • 批准号:
    23K08166
  • 财政年份:
    2023
  • 资助金额:
    $ 2.11万
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    Grant-in-Aid for Scientific Research (C)
Novel regenerative therapy for liver failure with skeletal myoblast cell sheet transplantation
骨骼肌成肌细胞片移植治疗肝衰竭的新型再生疗法
  • 批准号:
    22K08800
  • 财政年份:
    2022
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    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Hepatocytes Encapsulated with mesenchymal stromal cells in alginate microbeads for the treatment of acute Liver failure in Paediatric patients (HELP)
将间充质基质细胞封装在藻酸盐微珠中的肝细胞用于治疗儿科患者的急性肝衰竭(HELP)
  • 批准号:
    MR/V038583/1
  • 财政年份:
    2022
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Research Grant
New treatment methods for liver failure by human iPS cells
人类iPS细胞治疗肝衰竭的新方法
  • 批准号:
    22K08735
  • 财政年份:
    2022
  • 资助金额:
    $ 2.11万
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Checkpoint Inhibitors to Restore Monocyte/Macrophage Function in Liver Failure
检查点抑制剂可恢复肝衰竭患者的单核细胞/巨噬细胞功能
  • 批准号:
    MR/W015412/1
  • 财政年份:
    2022
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Research Grant
Pediatric Acute Liver Failure Immune Response Network (PALF IRN): Treatment for Immune Mediated Pathophysiology (TRIUMPH)
小儿急性肝衰竭免疫反应网络 (PALF IRN):免疫介导的病理生理学治疗 (TRIUMPH)
  • 批准号:
    10421290
  • 财政年份:
    2021
  • 资助金额:
    $ 2.11万
  • 项目类别:
Development of the innovative treatment using self iPS cell for acute liver failure
开发利用自身 iPS 细胞治疗急性肝衰竭的创新疗法
  • 批准号:
    21K08685
  • 财政年份:
    2021
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
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