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Effects of White Ginseng-Ejung-tand Acupuncture Solution on Nitric Oxide and Hydrogen peroxide Production in LPS-induced Mouse Macropnages

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경락경혈학회지 Vol.28, No.1, pp.61 69, 2011∼ Korean Journal of Acupuncture

Ji-Young Lee, Young-Jin Kim, Wan-Su Park College of Oriental Medicine, Kyung-Won University

Abstract

Objectives : The purpose of this study is to investigate effects of White Ginseng-Ejung-tang acupuncture solution (EJ) on nitric oxide (NO) and of hydrogen peroxide production in RAW 264.7 mouse macrophages stimulated by lipopolysaccharide (LPS).

Methods : Cell viability was measured by modified MTT assay. NO production was measured by Griess reagent assay. Hydrogen peroxide production was measured by dihydrorhodamine 123 (DHR) assay. Significant differences were examined by using a Student's t-test.

Results : The results of the experiment are as follows.

1. EJ did not show cell toxicity against RAW 264.7 cells for 24 hr incubation at the concentrations of up to 200 /mL in RAW 264.7 cells.

2. EJ significantly inhibited NO production for 24 hr incubation in RAW 264.7 cells (p<0.05).

3. EJ significantly inhibited the LPS-induced production of NO for 24 hr incubation in RAW 264.7 cells (p<0.05).

4. EJ significantly inhibited the LPS-induced production of hydrogen peroxide for 16, 24, 40, 48, 64, and 72 hr incubation in RAW 264.7 cells (p<0.05).

Conclusions : These results suggest that EJ has an anti-inflammtory property related with its inhibition of NO and hydrogen peroxide production in LPS-induced macrophages.

Key words : Ejung-tang, Macrophage, Inflammation, Nitric oxide, Hydrogen peroxide

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Fig. 1. Effect of EJ on cell viability in RAW 264.7 cells for 24 hr incubation.

Fig. 2. Effect of EJ on NO production in RAW 264.7 cells for 24 hr incubation.

Fig. 3. Effect of EJ on NO production in RAW 264.7 cells stimulated by LPS for 24 hr incubation.

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Fig. 4. Effect of EJ on the production of intracellular H2O2 in RAW 264.7 cells stimulated by LPS for 16 hr incubation.

H2O2 in RAW 264.7 cells for 24 hr incubation.

Fig. 6. Effect of EJ on the production of intracellular H2O2 in RAW 264.7 cells stimulated by LPS for 40 hr incubation.

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Fig. 7. Effect of EJ on the production of intracellular H2O2 in RAW 264.7 cells stimulated by LPS for 48 hr incubation.

Fig. 8. Effect of EJ on the production of intracellular H2O2 in RAW 264.7 cells stimulated by LPS for 64 hr incubation.

Fig. 9. Effect of EJ on the production of intracellular H2O2 in RAW 264.7 cells stimulated by LPS for 72 hr incubation.

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Fig. 2. Effect of EJ on NO production in RAW 264.7 cells for 24 hr incubation.
Fig. 4. Effect of EJ on the production of intracellular H 2 O 2 in RAW 264.7 cells stimulated by LPS for 16 hr incubation.
Fig. 9. Effect of EJ on the production of intracellular H 2 O 2 in RAW 264.7 cells stimulated by LPS for 72 hr incubation.

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