Neuroprotective effects of ginsenoside Rg3 against homocysteine-induced excitotoxicity in rat hippocampus

2007 
Abstract We previously demonstrated that ginsenoside Rg 3 (Rg 3 ), 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 Rg 3 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 Rg 3 on HC-induced hippocampal excitotoxicity in vitro and in vivo . Our in vitro studies using rat cultured hippocampal neurons revealed that Rg 3 treatment significantly and dose-dependently inhibited HC-induced hippocampal cell death, with an EC 50 value of 28.7 ± 7.5 μM. Rg 3 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 Rg 3 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 Rg 3 against HC-induced hippocampal excitotoxicity, we examined the effect of Rg 3 on HC-induced intracellular Ca 2+ elevations in cultured hippocampal cells and found that Rg 3 treatment dose-dependently inhibited HC-induced intracellular Ca 2+ elevation, with an IC 50 value of 41.5 ± 17.5 μM. In addition, Rg 3 treatment dose-dependently inhibited HC-induced currents in Xenopus oocytes expressing the NMDA receptor, with an IC 50 of 47.3 ± 14.2 μM. These results collectively indicate that Rg 3 -induced neuroprotection against HC in rat hippocampus might be achieved via inhibition of HC-mediated NMDA receptor activation.
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