کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4331538 | 1614303 | 2007 | 10 صفحه PDF | دانلود رایگان |
We previously demonstrated that ginsenoside Rg3 (Rg3), one of the active ingredients in Panax ginseng, attenuates NMDA receptor-mediated currents and NMDA-induced neurotoxicity (Kim, S., Kim, T., Ahn, K., Park, W.K., Nah, S.Y., Rhim, H., 2004. Ginsenoside Rg3 antagonizes NMDA receptors through a glycine modulatory site in rat cultured hippocampal neurons. Biochem. Biophys. Res. Commun. 323, 416-424). Accumulating evidence suggests that homocysteine (HC), a metabolite of methionine, exerts its excitotoxicity through NMDA receptor activation. In the present study, we examined the neuroprotective effects of Rg3 on HC-induced hippocampal excitotoxicity in vitro and in vivo. Our in vitro studies using rat cultured hippocampal neurons revealed that Rg3 treatment significantly and dose-dependently inhibited HC-induced hippocampal cell death, with an EC50 value of 28.7 ± 7.5 μM. Rg3 treatment not only significantly reduced HC-induced DNA damage, but also dose-dependently attenuated HC-induced caspase-3 activity in vitro. Our in vivo studies revealed that intracerebroventricular (i.c.v.) pre-administration of Rg3 significantly and dose-dependently reduced i.c.v. HC-induced hippocampal damage in rats. To examine the mechanisms underlying the in vitro and in vivo neuroprotective effects of Rg3 against HC-induced hippocampal excitotoxicity, we examined the effect of Rg3 on HC-induced intracellular Ca2+ elevations in cultured hippocampal cells and found that Rg3 treatment dose-dependently inhibited HC-induced intracellular Ca2+ elevation, with an IC50 value of 41.5 ± 17.5 μM. In addition, Rg3 treatment dose-dependently inhibited HC-induced currents in Xenopus oocytes expressing the NMDA receptor, with an IC50 of 47.3 ± 14.2 μM. These results collectively indicate that Rg3-induced neuroprotection against HC in rat hippocampus might be achieved via inhibition of HC-mediated NMDA receptor activation.
Journal: Brain Research - Volume 1136, 9 March 2007, Pages 190–199