Article ID Journal Published Year Pages File Type
1389977 Carbohydrate Research 2006 10 Pages PDF
Abstract

In this study, three novel maloyl glucans were isolated at temperatures below 15 °C from Aloe vera gel (Aloe barbadensis Miller). These compounds were characterized using NMR spectroscopy, ESIMS, MALDITOF-MS and capillary electrophoresis. The compounds were characterized as 6-O-(1-l-maloyl)-α-,β-d-Glcp (veracylglucan A), α-d-Glcp-(1→4)-6-O-(1-l-maloyl)-α,-β,-d-Glcp (veracylglucan B) and α-d-Glcp-(1→4)-tetra-[6-O-(1-l-maloyl)-α-d-Glcp-(1→4)]-6-O-(1-l-maloyl)-α,-β-d-Glcp (veracylglucan C). These unusual malic acid acylated carbohydrates were then tested in vitro for effects on cell proliferation and gene expression of proinflammatory cytokines, IL-6, IL-8 and ICAM-1, using RT-PCR. Veracylglucan B demonstrated potent anti-inflammatory and anti-proliferative effects, while Veracylglucan C, on the other hand, exhibited significant cell proliferative and anti-inflammatory activities. Veracylglucan A could only be isolated in smaller quantities, and it proved to be very unstable. Thus no biological effects could be observed in this respect. The in vitro bioassays also indicated that Veracylglucan B and C are antagonistic and competitive in their effects on cell proliferation. The results of this work represent a major step forward in the research on aloe vera gel. This is the first time that two fully chemically characterized compounds are shown to be responsible for known biological activities of aloe vera gel.

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Physical Sciences and Engineering Chemistry Organic Chemistry
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