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2001 Fiscal Year Final Research Report Summary

Analyses of SGLT1 function and cooperative function of SGLT1 with disaccharidase

Research Project

Project/Area Number 12672160
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 医薬分子機能学
Research InstitutionTokyo University of Pharmacy and Life Science

Principal Investigator

TAKASHI Mizuma  Tokyo University of Pharmacy and Life Science Department of Biophamaceutics,Associate Professor, 薬学部, 助教授 (80229715)

Co-Investigator(Kenkyū-buntansha) AKIRA Dobashi  Tokyo University of Pharmacy and Life Science Department of Stuctural Organic Chemistry,Professor, 薬学部, 教授 (40138962)
Project Period (FY) 2000 – 2001
Keywordsglucose transporter / glucose conjugate / glucoside / spare space / SGLT1 / transportability / recognition / disaccharidase
Research Abstract

Functionai analysis of SGLT1-mediated transport of glucose conjugates was performed. Influence of aglycone moiety on SGLT1 function was evaluated in terms of binding (recognition) and translocation (transport). All of glucose conjugates studied in this project, except salicin, were classified to Class T (transportable compound). Turnover of SGLT1for transport did not depend on molecular size. Furthrmore, although the order of turnover rate of p-substituents of phenyl β-glucose was NH_2 > OH > NO_2, binding affinity (Km) were similar to each other. This indicated that the binding and translocation of SGLT1 were affected by substituents, but the influcences were different. Molecular modeling analysis showed that glucose conformation of glucosides were in 4^C_1 chair form, which is the same as previous results (p-nitrophyeny1 β-glucoside and acetaminophen β-glucoside). Therefore, the position of spare apace of SGLT1 affects SGLT1 function.
Disaccharidase activities of disaccharide conjugate, maltase and LPH(lactase/phloridzin hydrolase) were found in Caco-2 cells. Furthermore, SGLT1 activity was detected in tri-iodothyronine-treated Caco-2 cells, although significant activity of SGLT1 was not detected i non-treated Caco-2 cells. This suggest that Caco-2 cells may be useful for the study of disaccharidase and SGLT1.

  • Research Products

    (8 results)

All Other

All Publications (8 results)

  • [Publications] Takashi Mizuma: "Intestinal transport and metabolism of glucose-conjugated kyotorphin and cyclic kyotorphin : metabolic degradation is crucial to intestinal absorption of peptide drugs"Biochim. Biophs. Acta. 1475. 90-98 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 水間 俊: "輸送担体および代謝酵素が関わる薬物腸管吸収の連続的過程よ競合的過程:SGLT1、二糖分解酵素、ペプチダーゼ、グルクロン酸抱合代謝酵素について"薬物動態. 16. 258-263 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takashi Mizuma: "Control and Diseases of Sodium Dependent Transport Proteins and Ion Channels"Elsevier. 440 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 水間 俊: "生物薬剤学(編 林、谷川原)"南江堂. 284 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takashi Mizuma et al.: "Intestinal transport and metabolism of glucoseconjugated kyotorphin and cyclic kyotorphin : metabolic degradation is crucial to intestinal absorption of peptide drugs,"Biochim.Biophys.Acta.. 1475. 90-98 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takashi Mizuma et al.: "Role of transporter and metabolic enzyme in sequential and competitive process of intestinal absorption : Study on SGLT1, disaccharidase and Pep tidase"Xenobiotic Metabolism and Disposition. 16. 258-263 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takashi Mizuma et al.: "Control and Diseases of Sodium DependentTransport Proteins and Ion Channels (Eds, Suketa etal.)"Elsevier. 440 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takashi Mizuma: "Biopharmaceutics (Eds. Hayashi and Tanigawara)"Nankodo. 284 (2001)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2003-09-17  

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