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Research Article

Chrysin, a Natural and Biologically Active Flavonoid, Influences a Murine Leukemia Model In Vivo through Enhancing Populations of T-and B-Cells, and Promoting Macrophage Phagocytosis and NK Cell Cytotoxicity

CHIN-CHUNG LIN, CHUN-SHU YU, JAI-SING YANG, CHI-CHENG LU, JO-HUA CHIANG, JING-PIN LIN, CHAO-LIN KUO and JING-GUNG CHUNG
In Vivo July 2012, 26 (4) 665-670;
CHIN-CHUNG LIN
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CHUN-SHU YU
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JAI-SING YANG
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CHI-CHENG LU
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JO-HUA CHIANG
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JING-PIN LIN
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CHAO-LIN KUO
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  • For correspondence: jgchung{at}mail.cmu.edu.tw clkuo{at}mail.cmu.edu.tw
JING-GUNG CHUNG
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  • For correspondence: jgchung{at}mail.cmu.edu.tw clkuo{at}mail.cmu.edu.tw
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    Figure 1.

    Chyrsin reduced the percentage of viable WEHI-3 cells. Cells were treated with 0, 5, 10, 20, 30, 40 and 50 μM chrysin for 24 and 48 h. The cells were harvested and the percentages of viable WEHI-3 cells were determined as described in Materials and Methods. Each point is the mean±S.D. of three experiments. *p<0.05, Significantly different compared with DMSO-treated control.

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    Figure 2.

    Representative mice after exposure to chrysin. Thirty male BALB/c mice were individually injected with WEHI-3 cells then randomly separated into three groups. Group I mice were treated with olive oil. Group II mice were treated with chrysin (10 mg/kg) in olive oil. Group III animals were treated with chrysin (50 mg/kg) in olive oil as described in the Materials and Methods. After sacrifice time, the blood and the spleen from all the animal was collected. NS: Not significant.

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    Figure 3.

    Chrysin affected the levels of cell markers in white blood cells from leukemic BALB/c mice. All mice were intraperitoneally injected with WEHI-3 cells for 2 weeks, followed by oral treatment with or without chrysin for 3 weeks. Blood was collected from each animal and was analyzed for cell markers (A: CD3; B: CD19; C: CD11b and D: Mac-3) by flow cytometry as described in Materials and Methods. The data are expressed as the mean±S.D. of three experiments (n=10). *p<0.05 Significant by different between control and chrysin-treated groups. NS: Not significant.

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    Figure 4.

    Chrysin stimulated phagocytotic activity of peripheral blood mononuclear cells (PBMCs) in leukemia BALB/c mice. Macrophages were isolated from PBMCs (A) and the peritoneal cavity (B) of each leukemic BALB/c mice after exposure to 0, 10 and 50 mg/kg/day of chrysin by oral administration for three weeks. The percentage of phagocytosis of green fluorescent particles (FITC-E.coli.) under chrysin treatment was determined by flow cytometric analysis as described in the Materials and Methods. Each point is mean±S.D (n=10). *p<0.05 Significant when compared with untreated leukemic mice. NS: Not significant.

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    Figure 5.

    Chrysin affected the activity of natural killer (NK) cells in leukemic BALB/c mice. The YAC-1 target cells were killed by NK cells of splenocytes from the mice after treatment with chrysin (10 and 50 mg/kg/day) by oral administration in target cell ratio of 25:1 and 50:1 Each point is the mean±S.D.*p<0.05 Significant when compared with untreated leukemic mice. NS: Not significant. (n=10).

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Vol. 26, Issue 4
July-August 2012
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Chrysin, a Natural and Biologically Active Flavonoid, Influences a Murine Leukemia Model In Vivo through Enhancing Populations of T-and B-Cells, and Promoting Macrophage Phagocytosis and NK Cell Cytotoxicity
CHIN-CHUNG LIN, CHUN-SHU YU, JAI-SING YANG, CHI-CHENG LU, JO-HUA CHIANG, JING-PIN LIN, CHAO-LIN KUO, JING-GUNG CHUNG
In Vivo Jul 2012, 26 (4) 665-670;

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Chrysin, a Natural and Biologically Active Flavonoid, Influences a Murine Leukemia Model In Vivo through Enhancing Populations of T-and B-Cells, and Promoting Macrophage Phagocytosis and NK Cell Cytotoxicity
CHIN-CHUNG LIN, CHUN-SHU YU, JAI-SING YANG, CHI-CHENG LU, JO-HUA CHIANG, JING-PIN LIN, CHAO-LIN KUO, JING-GUNG CHUNG
In Vivo Jul 2012, 26 (4) 665-670;
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