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姜黄素改善丝裂霉素C导致的肾功能损伤 被引量:1

Curcumin improves mitomycin C induced impairment of renal function
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摘要 目的探讨姜黄素对丝裂霉素C(MMC)导致的肾功能损伤的影响及作用机制。方法 制备人乳腺癌异种移植瘤裸鼠模型,2周后分别ip给予姜黄素100mg.kg-1,隔天1次,MMC1,1.5和2mg.kg-1,隔5d1次;姜黄素+MMC组各药的剂量与频率与单独用药一致,实验持续4周。观察动物体质量和存活率,测定瘤质量;采用液质联用仪检测药物在肾组织中的分布,测定血清肌酐(Cre)及血清尿素氮(BUN)含量。结果与正常对照组比,姜黄素100mg.kg-1与MMC1,1.5和2mg.kg-1联合用药组的实验动物食欲正常、无明显差异,且动物无死亡;单用MMC1.5和2mg.kg-1组动物存活率分别为4/8和7/8。与模型对照组相比,姜黄素联合MMC1,1.5和2mg.kg-1组肿瘤质量分别减少了40.9%,86.5%和82.7%,有显著性差异(P<0.05)。与单用MMC相比,姜黄素联合MMC1.5和2mg.kg-1用药后,Cre分别降低了25%和43%,BUN分别降低了41%和34%;肾组织中MMC药物含量分别减少了88%(P<0.01)和84%(P<0.01)。结论姜黄素可以减少MMC抑制肿瘤的用药量,并通过减少MMC在肾的分布,减轻其肾功能损伤。 OBJECTIVE To explore the mechanism of curcumin(Cur) improving mitomycin C(MMC) induced renal injury.METHODS MCF-7 breast cancer xenografts were set up on BALB/c nude mice.Cur 100 mg·kg-1 was ip given once a day,while MMC 1,1.5 and 2 mg·kg-1 was ip given once every 5 d.In Cur+MMC group,drug administration was at the same dosage and frequency as the single drug treatment.Body mass,the survival number and tumor mass were observed.The drug distribution in kidneys were detected by high performance liquid chromatography-mass spectrometry.Serum creatinine(Cre) and blood urea nitrogen(BUN) were determined.RESULTS The combination treatment of Cur and MMC resulted in eusitia of mice.No mice died in any group.However,the survival number of mice was 4/8 and 7/8 in MMC 1.5 and 2 mg·kg-1 alone groups,respectively.The impairment of renal function was induced by MMC 1.5 and 2 mg·kg-1.Compared with MMC group,serum Cre and BUN were reduced by 41% and 34% in Cur 100 mg·kg-1 combined with MMC 1.5 and 2 mg·kg-1 groups,respectively.Compared with MMC 1.5 and 2 mg·kg-1 groups,MMC distribution in kidneys in Cur+MMC 1 and 2.5 mg·kg-1 groups were reduced by 88%(P0.01) and 84%(P0.01),respectively.CONCLUSIONCur can reduce the dosage of MMC in breast cancer and improve MMC-induced impairment of renal function by reducing the distribution of MMC in kidneys.
出处 《中国药理学与毒理学杂志》 CAS CSCD 北大核心 2011年第4期375-379,共5页 Chinese Journal of Pharmacology and Toxicology
基金 上海市教委科研创新项目(08YZ54) 上海市教委E-研究院中医内科建设计划资助项目(E03008)~~
关键词 姜黄素 丝裂霉素C 肾功能 药物分布 curcumin mitomycin C renal function drug distribution
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参考文献8

  • 1Kim KH, Park HY, Nam JH, Park JE, Kim JY, Park MI, et al. The inhibitory effect of curcumin on the growth of human colon cancer cells ( HT-29, WiDr) in vitro [ J ]. Korean J Gastroenterol, 2005, 45 ( 4 ) : 277-284. 被引量:1
  • 2李昱辰,仲来福.姜黄素对顺铂所致大鼠肾毒性的防护作用[J].毒理学杂志,2006,20(2):91-93. 被引量:19
  • 3Zhou QM, Zhang H, Lu YY, Wang XF, Su SB. Cureu- min reduced the side effects of mitomycin C by inhibiting GRP58-mediated DNA cress-linking in MCF-7 breast cancer xenografts [ J ]. Cancer Sci, 2009, 100 ( 11 ) : 2040 -2045. 被引量:1
  • 4Volpato M, Seargent J, Loadman PM, Phillips RM. Formation of DNA interstrand cross-links as a marker of mitomycin C bioreductive activation and chemosensitivity [J]. Eur J Cancer, 2005, 41(9) :1331-1338. 被引量:1
  • 5Wu HI, Brown JA, Dorie M J, Lazzeroni L, Brown JM. Genome-wide identification of genes conferring resistance to the anticancer agents cisplatin, oxaliplatin, and mito- mycin C [ J ]. Cancer Res, 2004, 64 ( 11 ) : 3940-3948. 被引量:1
  • 6Campbell FC, Collett GP. Chemopreventive properties of cureumin[J]. Future Oncol, 2005, 1(3) :405-414. 被引量:1
  • 7Navis I, Sriganth P, Premalatha B. Dietary curcu- min with cisplatin administration modulates tumour marker indices in experimental fibrosarcoma [ J ]. Phar- macol Res, 1999, 39(3) :175-179. 被引量:1
  • 8苏成业.肾脏的药物代谢与肾脏病时药代动力学的改变.中国临床药理学杂志,1986,2(4):244-250. 被引量:1

二级参考文献12

  • 1Huasin K,Morris C,Whitworth C,et al.The deleterious effect of buthionine sulfoximine,a glutathione-depleting agent,on the cisplatin toxicity in mice.Jpn J Pharmacol,1990,52:652-655. 被引量:1
  • 2Somani SM,Ravi R,Rybak LP.Diethyldithiocarbamate protection against cisplatin nephrotoxicity:Antioxidant system.Drug Chem Toxicol,1995,18:151-170. 被引量:1
  • 3Green LM,Reade JL,Ware CF.Rapid colorimetric assay for cell viability:application to the quantitation of cytotoxic and growth inhibitory lymphokines.J Immunol Methods,1984,70:257-262. 被引量:1
  • 4Hannemann J,Baumann K.Cisplatin-induced lipid peroxidation and deCREase of gluconeogenesis in rat kidney cortex:different effects of antioxidants and radical scavengers.Toxicology,1988,51:119-132. 被引量:1
  • 5Kruidering M,Van WB,De HE,et al.Cisplatin-induced nephrotoxicity in porcine proximal tubular cells:mitochondrial dysfunction by inhibition of complexes Ⅰ to Ⅳ of the respiratory chain.J Pharmacol Exp Ther,1997,280:638-649. 被引量:1
  • 6Sreejayan,Rao MN.Cur cuminoids as potent inhibitors of lipid peroxidation.J Pharm Pharmacol,1994,46:1013-1016. 被引量:1
  • 7Rajakumar DV,Rao MN.Antioxidant properties of dehydrozingerone and curcumin in rat brain homogenates.Mol Cell Biochem,1994,140:73-79. 被引量:1
  • 8Sahu SC,Washington MC.Effect of ascorbic acid and curcumin on quercetin-induced nuclear DNA damage,lipid peroxidation and protein degradation.Cancer Lett,1992,63:237-241. 被引量:1
  • 9Kelly MR,Xu J,Alexander KE,et al.Disparate effects of similar phenolic phytochemicals as inhibitors of oxidative damage to cellular DNA.Mutat Res,2001,485:309-318. 被引量:1
  • 10杨一昆,普绍平,高文桂.顺铂的应用及铂族金属抗癌药物的研究进展[J].中国新药杂志,1999,8(12):797-800. 被引量:65

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