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DOI: 10.1055/s-0032-1309275
Die blutzuckersenkende und fettabbauende Aktivität der Bittermelone – Neue Erkenntnisse hinsichtlich der Wirkmechanismen
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Publication History
Publication Date:
05 November 2012 (online)
Zusammenfassung
Zur Bittermelone (Momordica charantia L.) gibt es mehr als 100 wissenschaftliche Publikationen, die einen Effekt bei der Blutzuckerregulation belegen. Eine Wirkung beim metabolischen Syndrom konnte erstmals nachgewiesen werden. Die angegebenen Wirkmechanismen für M. charantia waren bisher vorwiegend hypothetisch. So galt die Aktivierung von Inkretinen (intestinale, endokrine Hormone), die die Insulinfreisetzung stimulieren, als potenzieller Mechanismus oder die Resorptionshemmung von Glukose durch Hemmung von Glukosidasen und Disaccharasen im Intestinaltrakt. Neuerdings haben Wissenschaftler aus Kiel einen weiteren interessanten Interpretationsansatz gefunden. M.-charantia-Extrakt enthält einen spezifischen Hemmstoff der 11 β-Hydroxysteroid-Dehydrogenase Typ 1(11 β-HSD1), ein Enzym, das bei der Pathogenese von Diabetes und Adipositas eine Schlüssel rolle spielt und weltweit Ziel intensiver Forschung ist.
Summary
Improvement of glucose metabolism and weight lowering activity of bitter melon
There are more than 100 scientific publications supporting the blood sugar regulation effect of bitter melon (Momordica charantia L.). For the first time, however, an effect on the metabolic syndrome has been established. Hitherto, the mode of action of M. charantia was predominantly hypothetical. These included the activation of incretins (a group of gastrointestinal, endocrinal hormones) that stimulate an increase in the amount of insulin as potential mechanism or the resorption inhibition of glucose via the inhibition of glucosidases and disaccharases in the intestinal tract. As reported in this article, scientists from Kiel, Germany, have found a further new interesting approach regarding bitter melon. The extract from M. charantia contains a specific inhibitor of 11 β-hydroxysteroid dehydrogenase type 1 (11 β-HSD1), an enzyme that plays a key role in the pathogenesis of diabetes as well as obesity. It is a target candidate for worldwide research.
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