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. 2021 Jul 1;11:13690. doi: 10.1038/s41598-021-93086-y

Figure 5.

Figure 5

Increased intestinal permeability and the subsequent influx of PAMPs mediated by continuous alcohol administration to mice result in suppressed production of inflammatory cytokines from CD11b+ macrophages in the liver. (A) Study design. Control mice (n = 6) received a control liquid diet for 26 days. They were gavaged with isocaloric maltose dextrin twice per week for the last 6 weeks. Alcohol-treated mice (n = 6) received the control liquid diet for 5 days and the 5% ethanol liquid diet for 6 weeks. Withdrawal-group mice (n = 6) received the control liquid diet for 5 days and 5% ethanol liquid diet for 6 weeks, followed by feeding with the control liquid diet for 3 weeks as a withdrawal period. (B) Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. (C) Intestinal permeability evaluated by measuring the amount of fluorescence from dextran-FITC (Dx FITC) at 4 h after gavage. (D) Serum levels of TNF-α and IL-6. (E) Representative surface CD11b and intracellular TNF-α staining of liver mononuclear cells derived from the indicated mice, either unstimulated (upper) or stimulated with LPS for 4 h (lower). (F) Frequency of hepatic TNF-α producing CD11b+ macrophages from the indicated mice either unstimulated (upper) or stimulated with LPS for 4 h (lower). Data represent the mean ± SD. *p value < 0.05 by one-way ANOVA. N.S.: not significant. Data are representative from three independent experiments.