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格列奈类药物基因组学研究进展 被引量:1

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摘要 药物基因组学是在药物遗传学基础上发展起来的新兴学科,是分子药理学与功能基因组学结合的产物。通过研究药物代谢、转运及药物作用受体相关基因单核苷酸多态性(SNP)对药物疗效的影响,开发新药、指导临床合理用药,从而提高药物的疗效及安全性^[1]。候选基因主要包括药物代谢酶、药物转运蛋白以及药物受体基因。近年来对临床用药药物基因组学的研究日益增多,但有关糖尿病用药的研究尚少。随着糖尿病患病率的逐年升高,人们对糖尿病合理用药更加关注,这就促进了降糖药药物基因组学的发展。
出处 《上海医学》 CAS CSCD 北大核心 2008年第5期370-373,共4页 Shanghai Medical Journal
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  • 1Evans W E, Relling M V. Pharmacogenomics; translating functional genomics into rational therapeutics. Science, 1999,286: 487-491.
  • 2Goldberg R B, Einhorn D, Lucas C P, et al. A randomized placebo-controlled trial of repaglinlde in the treatment of type 2 diabetes. Diabetes Care, 1998, 21:1897-1903.
  • 3Niemi M, Leathart J B, Neuvonen M,et al. Polymorphism in CYP2C8 is associated with reduced plasma concentrations of repaglinide. Clin Pharmacol Ther, 2003,74 : 380 -387.
  • 4Kirchheiner J, Meineke I, Muller G, et al. Influence of CYP2C9 and CYP2D6 polymorphisms on the pharmacokine tics of nateglinide in genotyped healthy volunteers. Clin Pharmacokinet, 2004,43:267- 278.
  • 5Dai D, Zeldin D C, Blaisdell J A,et al. Polymorphisms in human CYP2C8 decrease metabolism of the anticancer drug paclitaxel and arachidonic acid. Pharmacogenetics, 2001, 11:597-607.
  • 6Bidstrup T B, Bjφrnsdottir I, Sidelmann U G,et al. CYP2C8and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repag linide.Br J Clin Pharmacol, 2003,56 : 305-314.
  • 7McLeod J F. Clinical pharmacokinetics of nateglinide: a rapidly-absorbed, short-acting insulinotropic agent. Clin Pharma cokinet, 2004,43: 97-120.
  • 8Klose T S, Blaisdell J A, Goldstein J A. Gene structure of CYP2C8 and extrahepatic distribution of the human CYP2Cs. J Biochem Mol Toxicol, 1999,13:289-295.
  • 9Niemi M, Backman J T, Neuvonen M,et al. Effects of gemfibrozil, itraconazole, and their combination on the pharmacokinetics and pharmacodynamics of repaglinide: potentially hazardous interaction between gemfibrozil and repaglinide. Diabetologia, 2003, 46: 347-351.
  • 10Bahadur N, Leathart J B, Mutch E,et al. CYP2C8 polymorphisms in Caucasians and their relationship with paclitaxel 6alpha-hydroxylase activity in human liver microsomes. Biothem Pharmacol, 2002,64:1579-1589.

同被引文献26

  • 1赵明,杜宏,王燕燕,王坚.磺脲类药物受体基因多态性和2型糖尿病、磺脲类药物疗效相关性初步研究[J].中华内科杂志,2003,42(11):808-809. 被引量:4
  • 2张伟,王安,周宏灏.口服降糖药的遗传药理学研究进展[J].中国临床药理学与治疗学,2007,12(1):7-10. 被引量:5
  • 3杨毅,郭丽敏,杨金奎.SUR1 Ser1369Ala多态性与磺脲类药物疗效的相关性[J].基础医学与临床,2007,27(5):521-524. 被引量:3
  • 4陈莉丽,李强,邢厚恂,任晓炜,孙玉倩,刘枫晨,梁梅花,张众,张巾超.磺脲类受体1基因多态性对磺脲类降糖药物作用的影响[J].第二军医大学学报,2007,28(7):765-767. 被引量:4
  • 5Nora N,Ana-Maria S,Darko K,et al.Metabolic control in type 2 diabetes is associated with sulfonyluren receptor-l (SUR-1) but not with KCNJI 1 polymorphisms[J].Arch Med Res,2009,40(5):387-392.
  • 6Marzena D,Hanna W,Pawel PJ.Impact of the sulfonylurea receptor 1(SUR1) exon 16-3c/t polymorphism on acute hyperglycaemia in type 2diabetic patients[J].Diabetes Res Clin Pract,2007,77(2):258-262.
  • 7Zhang HJ,Liu XM,Kuang HY,et al.Association of sulfonylurea receptor 1 genotype with therapeutic response to gliclazide in type 2 diabetes[J].Diabetes Res Clin Praet,2007,77(1):58-61.
  • 8de Morais SM,Schweikl H,Blaisdell J,et al.Gene structure and upstream regulatory regions of human CYP2C9 and CYP2C《,18》[J].Biothem Biophys Res Commun,1993,194(1):194-201.
  • 9Sullivan-Klose TH,Ghanayem BI,Bell DA,et al.The role of theCYP2C9-Leu359 allelic variant in the tolbutamide polymorphism[J].Pharmaeogenetics,1996,6(4):341-349.
  • 10Miners JO,Birken DJ.Cytoehrome P4502C9:an enzyme of major importance in human drug metabolism[J].Br J Clin Pharmacol,1998,45(6):525-538.

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