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Ginseng extract and total saponins suppress microglial activation in vitro and in vivo: implications for the treatment of Alzheimer's disease

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Ginseng extract and total saponins suppress microglial

activation in vitro and in vivo: implications for the

treatment of Alzheimer’s disease

Jin-Sun Park

1

, Eun-Mi Park

2

, Dong-Hyun Kim

3

, Hee-Sun Kim

1

1Department of Neuroscience and 2Department of Pharmacology, School of Medicine, Ewha Womans University, 3College of Pharmacy, Kyung Hee University, Seoul 110-783, Korea

The microglial activation plays an important role in the pathogenesis of Alzheimer’s disease by producing neurotoxic factors such as proinflammatory cytokines and nitric oxide (NO). Therefore, the inhibition of microglial activation would be an effective therapeutic approach to alleviating the progression of Alzheimer’s disease. In the present study, we investigated the effect of Korea Red Ginseng on microglial activation. Ginseng extract and total saponins suppressed LPS-induced release of NO, TNF-α,

and IL-6 in BV2 microglial cells. The inhibitory effect of total saponins was more potent than that of ginseng extract, suggesting that the main effective constituents harboring anti-inflammatory activity of red ginseng may be saponins. Similarly, ginseng extract and total saponins also suppressed Aβ-induced TNF-α

and IL-1β expression in microglial cells. RNase protection assay showed that ginseng extract and total

saponins regulated iNOS, MMP-9 and the cytokines at transcriptional level. Further mechanistic studies revealed that ginseng extract and total saponins significantly inhibited the MAPK and NF-κB activities in

LPS-stimulated microglial cells. Finally, the inhibitory effect of ginseng extract and total saponins on microglial activation was confirmed in LPS-injected mice. Therefore, the inhibition of microglial activation by ginseng extract and total saponins might have therapeutic potential for Alzheimer’s disease and other neurodegenerative diseases.

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