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Basic research for the prevention of cisplatin-induced renal toxicity based on the characteristics of renal tubular transport of its cytotoxic metabolite

Basic research for the prevention of cisplatin-induced renal toxicity based on the characteristics of renal tubular transport of its cytotoxic metabolite
基于顺铂细胞毒性代谢产物肾小管转运特性预防顺铂肾毒性的基础研究
批准号:
22790153
负责人:
IWAMOTO Takuya
金额:
$2.58万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Young Scientists (B)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2011

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中文摘要
翻译
研究顺铂N-乙酰半胱氨酸结合物(CDDP-NAC,细胞毒性代谢物)的肾小管转运特性。在转导OCT2、OAT1或OAT3的人胚胎肾293(HEK293)细胞中,CDDP-NAC在这些细胞中的积聚明显低于单独转染CDDP。NAC可抑制CDDP在肾小管上皮细胞的摄取,这可能是CDDP毒性降低的原因之一。
英文摘要
This study was performed to investigate the characteristics of renal tubular transport of N-acetylcysteine conjugate of cisplatin(CDDP-NAC, cytotoxic metabolite). In the human embryonic kidney 293(HEK293) cells transfected OCT2, OAT1 or OAT3, the CDDP-NAC accumulation in these cells was significantly lower than that of CDDP alone. NAC treatment prevented CDDP uptake in renal tubular cells, which might contribute to the reduced toxicity of CDDP.
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Concomitant use of itraconazole, a CYP3A4 inhibitor, increases the severity of peripheral neuropathy and thrombocytopenia induced by a protea some inhibitor, bortezomib
同时使用伊曲康唑(一种 CYP3A4 抑制剂)会增加由 Protea some 抑制剂硼替佐米引起的周围神经病变和血小板减少症的严重程度
DOI: --
发表时间: 2010
期刊: Pharmacotherapy
影响因子: 4.1
作者: [Iwamoto T, Ishibashi M, Fujieda A, Masuya M, Katayama N, Okuda M]
通讯作者: Okuda M
Altered function and expression of organic cation transporters, rOCT1 and rOCT2, in acute cholestasis and their implications in the disposition and clearances of drugs
急性胆汁淤积中有机阳离子转运蛋白 rOCT1 和 rOCT2 功能和表达的改变及其对药物处置和清除的影响
DOI: --
发表时间: 2010
期刊:
影响因子: --
作者: [Kurata, et al.]
通讯作者: et al.
DOI: 10.2133/dmpk.dmpk-10-rg-004
发表时间: 2010-01-01
期刊: DRUG METABOLISM AND PHARMACOKINETICS
影响因子: 2.1
作者: [Kurata, Tomohiko, Muraki, Yuichi, Okuda, Masahiro]
通讯作者: Okuda, Masahiro
Hepatic Drug Interaction Between Tacrolimus and Lansoprazole in a Bone Marrow Transplant Patient Receiving Voriconazole and Harboring CYP2C19 and CYP3A5 Heterozygous Mutations
接受伏立康唑且携带 CYP2C19 和 CYP3A5 杂合突变的骨髓移植患者中他克莫司和兰索拉唑之间的肝脏药物相互作用
DOI: --
发表时间: 2011
期刊: Clin Ther
影响因子: 3.2
作者: [Iwamoto T, Monma F, Fujieda A, Nakatani K, Katayama N, Okuda M]
通讯作者: Okuda M
The development of hepatic fibrosis suppression focusing on hepatic stellate cell energy metabolism
  • 批准号:
    17K15949
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.5万
  • 财政年份:
    2017
  • 负责人:
    IWAMOTO Takuya
  • 依托单位:
Development of therapy for liver cirrhosis : focused on energy metabolism of liver stellate cell
  • 批准号:
    15K19330
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.5万
  • 财政年份:
    2015
  • 负责人:
    IWAMOTO Takuya
  • 依托单位:
Risk evaluation of carboplatin-induced allergy based on basophil activation test and FceRI expression.
  • 批准号:
    24590188
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.41万
  • 财政年份:
    2012
  • 负责人:
    IWAMOTO Takuya
  • 依托单位:
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