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. Author manuscript; available in PMC: 2014 Apr 15.
Published in final edited form as: Biochem Pharmacol. 2013 Feb 5;85(8):1066–1076. doi: 10.1016/j.bcp.2013.01.026

Table 1.

Silymarin enhances the production of IFNγ and IL-12 by DCs obtained from UVB-irradiated wild-type mice but not DCs obtained from XPA-KO mice.

Cytokines Wild-type
XPA-KO
Control UVB SLM +UVB Control UVB SLM+ UVB
IFNγ 3989 1765 3010* 2508 1764 1883
IL-12 57 12 46* 21 5 7
IL-10 288 394** 300 203 339** 371

Wild-type and XPA-KO mice that were treated or not-treated with silymarin were exposed to UVB irradiation three times on consecutive days. Mice were sacrificed 24 h after the last UVB exposure and DCs (CD11c+ cells) were positively selected from the lymph nodes. DCs were stimulated with LPS (5μg/mL) for 48 h. After incubation, cells were harvested and supernatants collected. The concentrations of cytokines in the cell supernatants were estimated by ELISA. The data are presented as the mean in terms of pg/2 million cells, n=5.

Significant decrease versus non-UVB control, P<.001

*

significant increase versus UVB alone, P<0.001.

Significant decrease versus UVB alone, P<0.05.

**

Significant increase versus non-UVB control P<0.01.

SLM= silymarin.