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Research Article

Immuno- and Hepato-Toxicity of Dichloroacetic Acid in MRL+/+ and B6C3F1 Mice

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Pages 107-115 | Received 02 Oct 2006, Accepted 09 Dec 2006, Published online: 09 Oct 2008

Figures & data

TABLE 1 Body weight and liver/body weight ratios of MRL+/+ and B6C3F1 mice treated with DCA

FIG. 1 Serum levels of IgG and its subtypes in MRL+/+ (A) and B6C3F1 mice (B), and total IgM (C) in mice exposed to vehicle or DCA for 12 wk. The values represent the mean ± SEM (n = 6); *p < 0.05 when compared to the respective control.

FIG. 1 Serum levels of IgG and its subtypes in MRL+/+ (A) and B6C3F1 mice (B), and total IgM (C) in mice exposed to vehicle or DCA for 12 wk. The values represent the mean ± SEM (n = 6); *p < 0.05 when compared to the respective control.

FIG. 2 Serum levels of G-CSF and IL-12 in MRL+/+ and B6C3F1 mice exposed to vehicle or DCA for 12 wk. The values represent mean ± SEM (n = 6); *p < 0.05 when compared between strains.

FIG. 2 Serum levels of G-CSF and IL-12 in MRL+/+ and B6C3F1 mice exposed to vehicle or DCA for 12 wk. The values represent mean ± SEM (n = 6); *p < 0.05 when compared between strains.

FIG. 3 Levels of IL-10 and KC chemokine in liver extracts of MRL+/+ (A) and of multiple cytokines in liver extracts of B6C3F1 mice (B–D) exposed to vehicle or DCA for 12 wk. The values represent the mean ± SEM (n = 6); *p < 0.05 when compared to the respective control.

FIG. 3 Levels of IL-10 and KC chemokine in liver extracts of MRL+/+ (A) and of multiple cytokines in liver extracts of B6C3F1 mice (B–D) exposed to vehicle or DCA for 12 wk. The values represent the mean ± SEM (n = 6); *p < 0.05 when compared to the respective control.

FIG. 4 Cytokines secreted by splenic T-lymphocytes from MRL+/+ and B6C3F1 mice exposed to vehicle or DCA for 12 wk and activated in culture with antibodies against CD3 and CD8 for 48 hr. The values represent the mean (n = 6); *p < 0.05 for comparisons between mouse strain; #p < 0.05 for comparisons between control and DCA treatment within a strain.

FIG. 4 Cytokines secreted by splenic T-lymphocytes from MRL+/+ and B6C3F1 mice exposed to vehicle or DCA for 12 wk and activated in culture with antibodies against CD3 and CD8 for 48 hr. The values represent the mean (n = 6); *p < 0.05 for comparisons between mouse strain; #p < 0.05 for comparisons between control and DCA treatment within a strain.

FIG. 5 Liver histopathology of MRL+/+ (A and B) and B6C3F1 mice (C and D) exposed to vehicle (A and C) or DCA (B and D) for 12 wk. Liver sections were stained with H & E. Arrows indicate lipid accumulation within hepatocytes, compressing and displacing the nucleus to the periphery (magnification 200×).

FIG. 5 Liver histopathology of MRL+/+ (A and B) and B6C3F1 mice (C and D) exposed to vehicle (A and C) or DCA (B and D) for 12 wk. Liver sections were stained with H & E. Arrows indicate lipid accumulation within hepatocytes, compressing and displacing the nucleus to the periphery (magnification 200×).

FIG. 6 Liver histopathology of MRL+/+ (A and B) and B6C3F1 mice (C and D) exposed to vehicle (A and C) or DCA (B and D) for 12 wk. Liver sections were stained with Oil Red O (magnification 400×). Arrows indicate large intracellular lipid droplets.

FIG. 6 Liver histopathology of MRL+/+ (A and B) and B6C3F1 mice (C and D) exposed to vehicle (A and C) or DCA (B and D) for 12 wk. Liver sections were stained with Oil Red O (magnification 400×). Arrows indicate large intracellular lipid droplets.

FIG. 7 Quantification of Oil Red O staining of liver tissue from MRL+/+ and B6C3F1 mice exposed to vehicle or DCA for 12 wk. The values represent the mean ± SEM (n = 5); *p < 0.05 when compared to the respective control.

FIG. 7 Quantification of Oil Red O staining of liver tissue from MRL+/+ and B6C3F1 mice exposed to vehicle or DCA for 12 wk. The values represent the mean ± SEM (n = 5); *p < 0.05 when compared to the respective control.

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