Isoflavonoids from Astragalus mongholicus protect PC12 cells from toxicity induced by l-glutamate
lsoflavonoids, formononetin, 9,10-dimethoxypterocarpan 3- O-β- d-glucoside, ononin, calycosin 7- O-glc and calycosin, were isolated from the roots of Astragalus mongholicus Bunge (Leguminosae). The neuroprotective roles and direct antioxidant effects of these isoflavonoids were investigated by using...
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Published in | Journal of ethnopharmacology Vol. 98; no. 1; pp. 89 - 94 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Shannon
Elsevier Ireland Ltd
08.04.2005
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | lsoflavonoids, formononetin, 9,10-dimethoxypterocarpan 3-
O-β-
d-glucoside, ononin, calycosin 7-
O-glc and calycosin, were isolated from the roots of
Astragalus mongholicus Bunge (Leguminosae). The neuroprotective roles and direct antioxidant effects of these isoflavonoids were investigated by using PC12 cell model and DPPH (1,1-diphenyl-2-picrylhydrazyl) assay. Formononetin, ononin and calycosin were found inhibiting glutamate-induced cell injury, with an estimated 50% effective concentration (EC
50) of 0.027
μg/ml, 0.047
μg/ml and 0.031
μg/ml, respectively. Pretreatment with them increased the activities of antioxidant enzymes, including superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), and prevented the release of lactate dehydrogenase (LDH) in glutamate-injured PC12 cells. On the other hand, calycosin 7-
O-glc and calycosin showed more scavenging activity to DPPH radicals than formononetin in the cell-free system. The inconsistency between the neuroprotective capabilities of isoflavonoids and their directly scavenging activity to DPPH radicals indicated that formononetin, ononin and calycosin probably depended on increasing endogenous antioxidant and stabilizing the cells’ membrane structures to inhibit the cell damage induced by glutamate. |
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ISSN: | 0378-8741 1872-7573 |
DOI: | 10.1016/j.jep.2004.12.027 |