دورية أكاديمية

Piceatannol and Its Metabolite, Isorhapontigenin, Induce SIRT1 Expression in THP-1 Human Monocytic Cell Line

التفاصيل البيبلوغرافية
العنوان: Piceatannol and Its Metabolite, Isorhapontigenin, Induce SIRT1 Expression in THP-1 Human Monocytic Cell Line
المؤلفون: Shinpei Kawakami, Yosuke Kinoshita, Hiroko Maruki-Uchida, Koji Yanae, Masahiko Sai, Tatsuhiko Ito
المصدر: Nutrients, Vol 6, Iss 11, Pp 4794-4804 (2014)
بيانات النشر: MDPI AG, 2014.
سنة النشر: 2014
المجموعة: LCC:Nutrition. Foods and food supply
مصطلحات موضوعية: piceatannol, isorhapontigenin, resveratrol, sirtuin 1, THP-1, Nutrition. Foods and food supply, TX341-641
الوصف: Piceatannol is a phytochemical that is present in large amounts in passion fruit (Passiflora edulis) seeds, and is an analog of resveratrol. Recently, the absorption and metabolism of piceatannol were investigated in rats, and isorhapontigenin, O-methyl piceatannol, was detected as a piceatannol metabolite in rat plasma. To elucidate the function of piceatannol and its metabolites, we investigated the expression of sirtuin 1 (SIRT1) in THP-1 monocytic cells after treatment with piceatannol and its metabolites, and compared their effects with those of resveratrol and its metabolites. Piceatannol and resveratrol upregulated the expression levels of SIRT1 mRNA and SIRT1 protein. An extract of passion fruit seeds, which contained high levels of piceatannol, also upregulated SIRT1 mRNA expression. As for the metabolites, isorhapontigenin upregulated SIRT1 mRNA expression, whereas resveratrol glucuronides and sulfate did not affect SIRT1 expression. These findings indicate that after intake of piceatannol, not only piceatannol itself, but also its metabolite, isorhapontigenin, contributed to the upregulation of SIRT1 expression.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2072-6643
Relation: http://www.mdpi.com/2072-6643/6/11/4794; https://doaj.org/toc/2072-6643
DOI: 10.3390/nu6114794
URL الوصول: https://doaj.org/article/b9ec35ebc640476982a27a932216278a
رقم الأكسشن: edsdoj.b9ec35ebc640476982a27a932216278a
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20726643
DOI:10.3390/nu6114794