Protection of PC12 cells against superoxide-induced damage by isoflavonoids from Astragalus mongholicus.
- Author:
De-Hong YU
1
;
Yong-Ming BAO
;
Li-Jia AN
;
Ming YANG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Astragalus Plant; chemistry; Glucosides; chemistry; isolation & purification; pharmacology; Glutathione; metabolism; Glutathione Peroxidase; metabolism; Isoflavones; chemistry; isolation & purification; pharmacology; PC12 Cells; Protective Agents; isolation & purification; pharmacology; Proto-Oncogene Proteins c-bcl-2; metabolism; Rats; Superoxide Dismutase; metabolism; Xanthine Oxidase; antagonists & inhibitors; pharmacology
- From: Biomedical and Environmental Sciences 2009;22(1):50-54
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo further investigate the neuroprotective effects of five isoflavonoids from Astragalus mongholicus on xanthine (XA)/ xanthine oxidase (XO)-induced injury to PC12 cells.
METHODSPC12 cells were damaged by XA/XO. The activities of antioxidant enzymes, MTT, LDH, and GSH assays were used to evaluate the protection of these five isoflavonoids. Contents of Bcl-2 family proteins were determined with flow cytometry.
RESULTSAmong the five isoflavonoids including formononetin, ononin, 9, 10-dimethoxypterocarpan-3-O-beta-D-glucoside, calycosin and calycosin-7-O-glucoside, calycosin and calycosin-7-O-glucoside were found to inhibit XA/ XO-induced injury to PC12 cells. Their EC50 values of formononetin and calycosin were 0.05 microg/mL. Moreover, treatment with these three isoflavonoids prevented a decrease in the activities of antioxidant enzymes, superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), while formononetin and calycosin could prevent a significant deletion of GSH. In addition, only calycosin and calycosin-7-O-glucoside were shown to inhibit XO activity in cell-free system, with an approximate IC50 value of 10 microg/mL and 50 microg/mL. Formononetin and calycosin had no significant influence on Bcl-2 or Bax protein contents.
CONCLUSIONNeuroprotection of formononetin, calycosin and calycosin-7-O-glucoside may be mediated by increasing endogenous antioxidants, rather by inhibiting XO activities or by scavenging free radicals.