11β-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches

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• 作者：Judith M. Rollinger ; Denise V. Kratschmar ; Daniela Schuster ; Petra H. Pfisterer ; Christel Gumy ; Evelyne M. Aubry ; Sarah Br ; stö ; tter ; Hermann Stuppner ; Gerhard Wolber ; Alex Odermatt
• 关键词：Eriobotrya japonica ; 11β ; -HSD1 ; Diabetes ; Glucocorticoid receptor ; Metabolic syndrome
• 刊名：Bioorganic and Medicinal Chemistry
• 出版年：2010
• 出版时间：15 February 2010
• 年：2010
• 卷：18
• 期：4
• 页码：1507-1515
• 全文大小：684 K

文摘

The inhibition of 11β-hydroxysteroid dehydrogenase 1 (11β-HSD1), which catalyzes the conversion of inactive 11-ketoglucocorticoids to active 11β-hydroxyglucocorticoids, emerged as promising strategy to treat symptoms of the metabolic syndrome, including obesity and type 2 diabetes. In this study the leaves of the anti-diabetic medicinal plant loquat (Eriobotrya japonica) were phytochemically investigated following hints from a pharmacophore-based virtual screening and a bioactivity-guided approach. Determination of the 11β-HSD1 and 11β-HSD2 inhibitory activities in cell lysates revealed triterpenes from the ursane type as selective, low micro-molar inhibitors of 11β-HSD1, that is, corosolic acid (1), 3-epicorosolic acid methyl ester (4), 2-α hydroxy-3-oxo urs-12-en-28-oic acid (6), tormentic acid methyl ester (8), and ursolic acid (9). Importantly, a mixture of loquat constituents with moderate activities displayed a pronounced additive effect. By means of molecular modeling studies and the identification of the 11β-HSD1-inhibiting 11-keto-ursolic acid (17) and 3-acetyl-11-keto-ursolic acid (18) a structure–activity relationship was deduced for this group of pentacyclic triterpenes. The mechanism of action elucidated in the present work together with the previously determined pharmacological activities provides these natural products with an astonishing multi-targeted anti-diabetic profile.