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Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property.

Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property. Research Abstract Details 

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  • Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property. Abstract Text:

    kwong-fai wongKwong-Fai Wong,jacqueline k chanJacqueline K Chan,kwong-leung chanKwong-Leung Chan,paul tamPaul Tam,dan yangDan Yang,sheung-tat fanSheung-Tat Fan,john m lukJohn M Luk,kwong-fai wongKwong-Fai Wong,jacqueline k chanJacqueline K Chan,kwong-leung chanKwong-Leung Chan,paul tamPaul Tam,dan yangDan Yang,sheung-tat fanSheung-Tat Fan,john m lukJohn M Luk,kwong-fai wongKwong-Fai Wong,jacqueline k chanJacqueline K Chan,kwong-leung chanKwong-Leung Chan,paul tamPaul Tam,dan yangDan Yang,sheung-tat fanSheung-Tat Fan,john m lukJohn M Luk,

    1. Tripterygium wilfordii (TW) contains bioactive compounds that possess immunosuppressive properties. These compounds are considered to be potential drugs in the treatment of acute graft rejections. However, their structure-activity relationships remain unknown. 2. The aim of the present study was to delineate the molecular moieties of triptolide that could account for its ability to inhibit inflammatory responses. In this context, purified TW active compounds (triptolide and triptonide) and synthetic triptolide derivatives were prepared to investigate the structure-activity relationships of triptolide. To this end, rat splenocytes were treated with increasing concentrations of the compounds and then allogenically stimulated using a mixed lymphocyte reaction to determine their antiproliferative activities. From the results, the IC(50) value of each compound was calculated. 3. Modification of the beta-hydroxyl group at the C-14 position of the triptolide molecule significantly affected the immunosuppressive activity of T59, as demonstrated by a sevenfold increase of the IC(50). Conversely, reduction of the gamma-butyrolactone group in T60 and T61 completely abrogated the antiproliferative effect. Alterations in the C-14 beta-hydroxyl and gamma-butyrolactone groups also resulted in reduced cytotoxicity. 4. The present findings demonstrate that the C-14 beta-hydroxyl and gamma-butyrolactone moieties of the triptolide molecule are crucial for its anti-inflammatory properties and cytotoxicity and are responsible for the compound's antiproliferative activity.

    Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property. Publishing Authors By Initials

    kf wongKF Wong,jk chanJK Chan,kl chanKL Chan,p tamP Tam,d yangD Yang,st fanST Fan,jm lukJM Luk,kf wongKF Wong,jk chanJK Chan,kl chanKL Chan,p tamP Tam,d yangD Yang,st fanST Fan,jm lukJM Luk,kf wongKF Wong,jk chanJK Chan,kl chanKL Chan,p tamP Tam,d yangD Yang,st fanST Fan,jm lukJM Luk,

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    Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Clinical and experimental pharmacology & physiolog

    VOLUME: 35

    Page Numbers: 55-9

    Journal Abbreviation: Clin. Exp. Pharmacol. Physiol.

    ISSN: 0305-1870

    DAY: 30

    MONTH: Jan

    YEAR: 2008

    Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 425076

    Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property. Keywords Mesh Terms:

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    Grant and Affiliation Information for Immunochemical characterization of the functional constituents of tripterygium wilfordii contributing to its anti-inflammatory property.

    AFFILIATION: Department of Surgery, University of Hong Kong, Jockey Club Clinical Research Center, Pokfulam, Hong Kong.

    Country: Australia

    Australia Research PublicationAustralia Research Publication

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    MEDLINETA: Clin Exp Pharmacol Physiol

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