课题基金 / 基金详情

Physiological Function of Hormones Derived from Mesenchymal Cells and Its Failure

Physiological Function of Hormones Derived from Mesenchymal Cells and Its Failure
间充质细胞激素的生理功能及其失效
批准号:
21229013
负责人:
NAKAO Kazuwa
金额:
$135.62万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (S)
财政年份:
2009
资助国家:
日本
项目状态:
已结题
起止时间:
2009-05-11 至 2014-03-31

项目摘要

项目成果

NAKAO Kazuwa的其他基金

相关文献

中文摘要
翻译
我们证明了CNP ecKO小鼠的BP显著升高。肠系膜动脉血管舒张反应明显减弱。我们发现,循环CNP拯救软骨发育不良的CNP ko小鼠骨骼生长受损。我们揭示了GC-A保护足细胞免受醛固酮诱导的肾小球损伤,我们证明了脂肪营养不良患者通过fMRI和饱腹感对食物相关神经活动的餐后抑制不足,瘦素可以恢复这种抑制,并且瘦素/胰淀素联合给药对DIO小鼠的糖和脂质代谢具有有益作用。由于我们的制造商发起的试验,用于脂肪代谢障碍的重组人瘦素的上市和生产于2013年在日本获得批准。我们在体外证明了人iPS/ES细胞的成脂潜能,并且这些脂肪细胞在移植后可以存活至少4周。
英文摘要
We demonstrated that the BP of CNP ecKO mice is significantly elevated. Their vascular relaxation reaction of mesenteric artery was diminished significantly. We showed that circulating CNP rescues chondrodysplastic CNP ko mice from impaired skeletal growth. We revealed that GC-A protects podocytes from aldosterone-induced glomerular injury.We demonstrated the insufficiency of postprandial suppression of food-related neural activity by fMRI and satiety feeling in lipodystrophic patients, which was restored by leptin, and that the beneficial effect of leptin /amylin coadministration on glucose and lipid metabolism in DIO mice. Owing to our investigator-initiated trial, marketing and manufacturing of recombinant human leptin for lipodystrophy were approved in 2013 in Japan. We demonstrated on adipogenic potential of human iPS/ES cells in vitro, and that these adipocytes can survive for at least 4 weeks after transplantation.
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DOI: 10.1007/s00223-011-9567-0
发表时间: 2012-04-01
期刊: CALCIFIED TISSUE INTERNATIONAL
影响因子: 4.2
作者: [Kondo, Eri, Yasoda, Akihiro, Nakao, Kazuwa]
通讯作者: Nakao, Kazuwa
DOI: 10.2337/dc09-1447
发表时间: 2010-05
期刊: Diabetes care
影响因子: 16.2
作者: [Yasuno S, Ueshima K, Oba K, Fujimoto A, Hirata M, Ogihara T, Saruta T, Nakao K]
通讯作者: Nakao K
DOI: 10.1507/endocrj.k10e-164
发表时间: 2010-08
期刊: Endocrine journal
影响因子: 2
作者: [A. Yasoda;K. Nakao]
通讯作者: A. Yasoda;K. Nakao
DOI: 10.1038/ki.2011.305
发表时间: 2012-01
期刊: Kidney international
影响因子: 19.6
作者: [H. Yokoi;M. Kasahara;K. Mori;Y. Ogawa;T. Kuwabara;Hirotaka Imamaki;T. Kawanishi;Kenichi Koga;]
通讯作者: H. Yokoi;M. Kasahara;K. Mori;Y. Ogawa;T. Kuwabara;Hirotaka Imamaki;T. Kawanishi;Kenichi Koga;
78
    Development and analysis of model rats for diseases of endocrinology and metabolism
    • 批准号:
      23659476
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.33万
    • 财政年份:
      2011
    • 负责人:
      NAKAO Kazuwa
    • 依托单位:
    Translational research and development of novel diagnostic/therapeutic modalities for metabolic syndrome based on adipocyte endocrinology and adiposcience
    • 批准号:
      16109007
    • 项目类别:
      Grant-in-Aid for Scientific Research (S)
    • 资助金额:
      $73.22万
    • 财政年份:
      2004
    • 负责人:
      NAKAO Kazuwa
    • 依托单位:
    Molecular Basis of Centrally-controled Energy Homeostasis -Focusing on Leptin Resistance-
    • 批准号:
      13307033
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $35.36万
    • 财政年份:
      2001
    • 负责人:
      NAKAO Kazuwa
    • 依托单位:
    Clinical implication of cardiovascular hormones
    • 批准号:
      10307026
    • 项目类别:
      Grant-in-Aid for Scientific Research (A).
    • 资助金额:
      $24.83万
    • 财政年份:
      1998
    • 负责人:
      NAKAO Kazuwa
    • 依托单位: