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有机阴离子转运多肽1A2对药物转运的影响 被引量:1

Effect on drug transport of OATP1A2
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摘要 有机阴离子转运多肽1A2(OATP1A2)是人体内重要的膜转运蛋白,在肝、肾、小肠、血脑屏障等组织部位进行表达,介导内、外源物质的跨细胞转运,对药物的吸收、分布和消除起着十分重要的作用。本文将对OATP1A2的组织分布和基本功能、基因多态性及其对药物转运的影响作一综述。 Organic anion transporting polypeptide 1A2(OATP1A2),expressed in liver, kidney,small intestine,blood-brain barrier and other organizations,is an important membrane transporter in humans.OATP1A2 mediates the trans-membrane transport of endogenous and exogenous materials,and plays a significant role in drug absorption,distribution and elimination. This review aimes to summarize the distribution, basic functions and gene polymorphism of OATP1A2,and its impact on drug transport.
出处 《中国临床药理学与治疗学》 CAS CSCD 2010年第4期464-469,共6页 Chinese Journal of Clinical Pharmacology and Therapeutics
关键词 有机阴离子转运多肽1A2 药物转运 药代动力学 Organic anion transporting polypeptide 1A2 Drug transport Pharmacokinetics
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参考文献31

  • 1Zair ZM, Eloranta JJ, Stieger B, et al. Pharmacogenetics of OATP (SLC21/SLCO), OAT and OCT (SLC22) and PEPT (SLC15) transporters in the intestine, liver and kidney[J].Pharmacogenomics, 2008, 9(5): 597-624.
  • 2张伟,贺毅憬,周宏灏.有机阴离子转运多肽1B1的遗传药理学进展[J].中国临床药理学与治疗学,2008,13(7):721-729. 被引量:16
  • 3Hagenbuch B, Meier PJ. The superfamily of organic anion transporting polypeptides[J]. Biochin Bio phys Acta, 2003, 1609(1): 1-18.
  • 4Kullak-Uhlick GA, Hagenbuch B, Stieger B, et al. Molecular and functional characterization of an organic anion transporting polypeptide cloned from human liver[J]. Gastroenterology, 1995, 109(4): 1274-1282.
  • 5Steekelbroeck S, Nassen A, Ugele B, et al. Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunhistochemistry study[J]. Neurochem, 2004, 89 (2) : 403-417.
  • 6Noe B, Hagenbuch B, Stieger B, et al. Isolation of a muhispecific organic anion and cardiac glycoside transporter from rat brain[J]. Proc Natl Acad Sci USA, 1997, 94(19): 10346-10350.
  • 7Badagnani I, Castro R, Taylor T, et al. Interaction of methotrexate with organic-anion transporting polypeptide 1A2 and its genetic variants[J]. Pharmacol Exp Ther, 2006, 318(2): 521-529.
  • 8Franke RM, Scherkenbach I.A, Sparreboom A. Pharmacogenetics of the organic anion transporting polypeptide 1A2[J]. Pharmacogenomics, 2009, 10 (3): 339-344.
  • 9Ho RH. Tirona RG, Leake BF,et al. Drug and bile acid transporters in rosuvastatin hepatic uptake: function, expression and pharmacogenetics[J]. Gastroenterology, 2006, 130(6):1793-1806.
  • 10Maeda T, Takahashi K, Ohtsu N, et al. Identification of influx transporter for the quinolone antibacterial agent levofloxacin[J]. Mol Pharm, 2007, 4 (1):85-94.

二级参考文献55

  • 1Takeda M, Sekine T, Endou H. Regulation by protein kinase C of organic anion transport driven by rat organic anion transporter 3 ( rOAT3 ). Life Sci, 2000,67 (9) : 1087-1093.
  • 2Braeunlich H. Transport of p-aminobhippurate in renal corti-cal slices of rats of different ages following treatement with thyroid hormones. Biomed Biochim Acta, 1987, 46 (4): 251-257.
  • 3Buist SC, Cherrington NJ. Klaassen CD. Endocrine regulation of rat organic anion transporters. Drug Metab Dispos, 2003,31 (5) : 559-564.
  • 4Buist SC, Klassen CD. Rat and mouse differences in genderpredominant expression of organic anion transporter ( OAT1- 3 ; slczza 6-8 ) maRNA levels. Drug Metab Dispos, 2004,32 (6) :620-625.
  • 5Maher JM, Slitt AL, Callaghan TN, et al. Aherations in transporter expression in liver, kidney, and duodenum after targeted disruption of the transcription factor HNF1α. Biochem Pharmacol, 2006, 72(4) :512-522.
  • 6Jariyawat S, Sekine T, Takeda M, et al. The interaction and transport of beta-lactam antibiotics with the cloned rat renal organic anion transporter 1. J Pharmacol Exp Ther, 1999, 290(2) :672-677.
  • 7Vanwert AL, Bailey RM, Sweet DH. Organic anion transporter 3 (Oat3/Slc22a8) knockout mice exhibit altered clearance and distribution of penicillin G. Am J Physiol Renal Physiol, 2007,293(4) : 1332-1341.
  • 8Ho ES, Lin DC, Mendel DB, et al. Cytotoxicity of antiviral nucleotides adefovir and cidofovir is induced by the expression of human renal organic anion transporter 1. J Am Soc Nephrol, 2000,11 (3) :383-393.
  • 9Khamdng S, Takeda M, Noshiro R, et al. Interactions of human organic anion transporters and human organic cation transporters with nonsteroidal anti-inflammatory durgs. J Pharmacol Exp Ther, 2002,303 (2) :534-539.
  • 10Hasannejad H, Takeda M, Taki K, et al. Interactions of human organic anion transporters with diuretics. J Pharmacol Exp Ther, 2003,308 (3) : 1021-1029.

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  • 1J edlitschky G, Hoffmann U, Kroemer HK. Struc-ture and function of the MRP2 (ABCC2) protein and its role in drug disposition[J]. Expert Opin Drug Metab Toxicol , 2006, 2(3): 351-366.
  • 2Boaglio AC, Zucchetti AE, Sanchez Pozzi EI, et al. Phosphoinositide 3-kinase/protein kinase B signa-ling pathway is involved in estradiol 17-D-glucu-ronide-induced cholestasis . complementarity with classical protein kinase C[J]. Hepatology, 2010, 52(4): 1465-1476.
  • 3Lau vv, Wu CY, Okochi H, et al. Ex situ inhibi-tion of hepatic uptake and efflux significantly chan-ges metabolism: hepatic enzyme-transporter inter-play[J]. 1 Pharmacol Exp Ther, 2004, 308 (3): p. 1040-1045.
  • 4Hartman IC, Brouwer K. Mandagere A, et al. E-valuation of the endothelin receptor antagonists am-brisentan , darusentan , bosentan , and sitaxsentan as substrates and inhibitors of hepatobiliary transport-ers in sandwich-cultured human hepatocytes[J]. Can 1 Physiol Pharmacol, 2010. 88(6): 682-69l.
  • 5Gao B, Hagenbuch B. Kullak-Ublick GA, et al. Organic anion-transporting polypeptides mediate transport of opioid pep tides across blood-brain bar-rier[J]. 1 Pharmacol Exp Ther, 2000,294 (1): 73 -79.
  • 6Weber SI. Greene DL, Sharma SD, et al. Distribu-tion and analgesia of[3HJ[D-Pen2, D-Pen5J en-kephalin and two halogenated analogs after intrave-nous administration[J]. 1 Pharmacol Exp Ther, 1991, 259(3): 1109-1117.
  • 7Chen C, Pollack GM. Extensive biliary excretion of the model opioid peptide[D-PEN2, 5J enkephalin in rats[J]. Pharm Res, 1997, 14(3): 345-350.
  • 8Hoffmaster KA, Zamek-Gliszczynski MI. Pollack GM, et al. Multiple transport systems mediate the hepatic uptake and biliary excretion of the metaboli-cally stable opioid peptide[D-penicillamine2, 5J en-kephalin[J]. Drug Metab Dispos , 2005, 33 (2) : 287-293.
  • 9Hoffmaster KA, Zamek-Gliszczynski MI, Pollack GM, et al. Hepatobiliary disposition of the meta-bolically stable opioid peptide[D- Pen2, D- Pen5J-enkephalin (DPDPE): pharmacokinetic conse-quences of the interplay between multiple transport systems[J].J Pharmacol Exp Ther, 2004, 311 (3): 1203-1210.
  • 10Kotani N, Maeda K, Watanabe T, et al, Culture period-dependent changes in the uptake of trans-porter substrates in sandwich-cultured rat and hu-man hepatocytes[J]. Drug Metab Dispos , 2011, 39(9): 1503-1510.

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