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  • 标题:Effects of Polymorphisms of MDR1, MRP1, and MRP2 Genes on Their mRNA Expression Levels in Duodenal Enterocytes of Healthy Japanese Subjects
  • 本地全文:下载
  • 作者:Yuka Moriya ; Tsutomu Nakamura ; Masanori Horinouchi
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2002
  • 卷号:25
  • 期号:10
  • 页码:1356-1359
  • DOI:10.1248/bpb.25.1356
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:In the present study, we examined whether polymorphisms in the ATP-binding cassette (ABC) transporter genes, MDR1 , MRP1 and MRP2 , were associated with their respective mRNA expression levels in duodenal enterocytes of 13 healthy Japanese volunteers. MDR1 genotypes of T-129C, G2677(A,T) and C3435T, MRP1 genotypes of G128C, C218T, G2168A and G3173A, and MRP2 genotypes of C-24T, G1249A, C2302T, C2366T and G4348A were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) or direct sequencing. Mutations T-129C, G2677(A,T) and C3435T of MDR1 gene were found at allele frequencies of 2/26, 16/26 and 12/26, respectively. Mutations G2168A of the MRP1 gene and C-24T of the MRP2 gene were also found at allele frequencies of 1/26 and 6/26, respectively, whereas other mutations were not detected in MRP1 and MRP2 genes. The relative concentrations (mean±S.E.) of MDR1 mRNA to villin mRNA were 0.38±0.15, 0.56±0.14 and 1.13±0.42 in the subjects with C/C3435, C/T3435 and T/T3435, respectively, which supported the lower serum concentrations of digoxin after single oral administration in the subjects with the mutant T-allele at position 3435. Genetic collaboration between positions 3435 and 2677 was suggested, and those in G/G2677, G/(A,T)2677 and T/(A,T)2677 were 0.16±0.05, 1.10±0.40, and 0.63±0.16, respectively ( p =0.107). However, there was no remarkable effect of the G2168A of the MRP1 gene or of C-24T of the MRP2 gene on the relative MRP1 or MRP2 mRNA concentrations, respectively.
  • 关键词:P-glycoprotein;multidrug resistance-associated protein;genetic polymorphism;gene expression;duodenal enterocyte
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