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Colonic and plasmatic food intake regulation in female and male TLR4 IEC −/− mice in response to the ABA model. Relative cDNA levels of the Gcg and <t>Pyy</t> genes in female (A) and male (B) mice. Plasmatic concentration of the anorexigenic <t>hormones</t> <t>GLP1</t> and PYY in female (C) and male (D) mice. Wild-type ( wt ) mice (in blue) and mice invalidated for the TLR4 specifically in intestinal epithelial cells (TLR4 IEC −/− , in red), were submitted to the activity-based anorexia (ABA) model or were used under control conditions (CTs). The data are shown as mean ± SEM and were analyzed using two-way ANOVA (TLR4 IEC −/− × ABA). The two-way ANOVA significance ( p < 0.05 or ABA, TLR4 IEC −/− and/or Int for interaction) is indicated by bold and underlined font. Tukey's multiple comparisons test results are indicated as * p < 0.05, *** p < 0.001. n and exact p- value on Figure S10.
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Colonic and plasmatic food intake regulation in female and male TLR4 IEC −/− mice in response to the ABA model. Relative cDNA levels of the Gcg and <t>Pyy</t> genes in female (A) and male (B) mice. Plasmatic concentration of the anorexigenic <t>hormones</t> <t>GLP1</t> and PYY in female (C) and male (D) mice. Wild-type ( wt ) mice (in blue) and mice invalidated for the TLR4 specifically in intestinal epithelial cells (TLR4 IEC −/− , in red), were submitted to the activity-based anorexia (ABA) model or were used under control conditions (CTs). The data are shown as mean ± SEM and were analyzed using two-way ANOVA (TLR4 IEC −/− × ABA). The two-way ANOVA significance ( p < 0.05 or ABA, TLR4 IEC −/− and/or Int for interaction) is indicated by bold and underlined font. Tukey's multiple comparisons test results are indicated as * p < 0.05, *** p < 0.001. n and exact p- value on Figure S10.
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Colonic and plasmatic food intake regulation in female and male TLR4 IEC −/− mice in response to the ABA model. Relative cDNA levels of the Gcg and <t>Pyy</t> genes in female (A) and male (B) mice. Plasmatic concentration of the anorexigenic <t>hormones</t> <t>GLP1</t> and PYY in female (C) and male (D) mice. Wild-type ( wt ) mice (in blue) and mice invalidated for the TLR4 specifically in intestinal epithelial cells (TLR4 IEC −/− , in red), were submitted to the activity-based anorexia (ABA) model or were used under control conditions (CTs). The data are shown as mean ± SEM and were analyzed using two-way ANOVA (TLR4 IEC −/− × ABA). The two-way ANOVA significance ( p < 0.05 or ABA, TLR4 IEC −/− and/or Int for interaction) is indicated by bold and underlined font. Tukey's multiple comparisons test results are indicated as * p < 0.05, *** p < 0.001. n and exact p- value on Figure S10.
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Colonic and plasmatic food intake regulation in female and male TLR4 IEC −/− mice in response to the ABA model. Relative cDNA levels of the Gcg and <t>Pyy</t> genes in female (A) and male (B) mice. Plasmatic concentration of the anorexigenic <t>hormones</t> <t>GLP1</t> and PYY in female (C) and male (D) mice. Wild-type ( wt ) mice (in blue) and mice invalidated for the TLR4 specifically in intestinal epithelial cells (TLR4 IEC −/− , in red), were submitted to the activity-based anorexia (ABA) model or were used under control conditions (CTs). The data are shown as mean ± SEM and were analyzed using two-way ANOVA (TLR4 IEC −/− × ABA). The two-way ANOVA significance ( p < 0.05 or ABA, TLR4 IEC −/− and/or Int for interaction) is indicated by bold and underlined font. Tukey's multiple comparisons test results are indicated as * p < 0.05, *** p < 0.001. n and exact p- value on Figure S10.
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Colonic and plasmatic food intake regulation in female and male TLR4 IEC −/− mice in response to the ABA model. Relative cDNA levels of the Gcg and Pyy genes in female (A) and male (B) mice. Plasmatic concentration of the anorexigenic hormones GLP1 and PYY in female (C) and male (D) mice. Wild-type ( wt ) mice (in blue) and mice invalidated for the TLR4 specifically in intestinal epithelial cells (TLR4 IEC −/− , in red), were submitted to the activity-based anorexia (ABA) model or were used under control conditions (CTs). The data are shown as mean ± SEM and were analyzed using two-way ANOVA (TLR4 IEC −/− × ABA). The two-way ANOVA significance ( p < 0.05 or ABA, TLR4 IEC −/− and/or Int for interaction) is indicated by bold and underlined font. Tukey's multiple comparisons test results are indicated as * p < 0.05, *** p < 0.001. n and exact p- value on Figure S10.

Journal: Gut Microbes

Article Title: Intestinal epithelial TLR4 knock out induces sex-specific effects on gut barrier and microbiome in an activity-based anorexia model

doi: 10.1080/19490976.2026.2637316

Figure Lengend Snippet: Colonic and plasmatic food intake regulation in female and male TLR4 IEC −/− mice in response to the ABA model. Relative cDNA levels of the Gcg and Pyy genes in female (A) and male (B) mice. Plasmatic concentration of the anorexigenic hormones GLP1 and PYY in female (C) and male (D) mice. Wild-type ( wt ) mice (in blue) and mice invalidated for the TLR4 specifically in intestinal epithelial cells (TLR4 IEC −/− , in red), were submitted to the activity-based anorexia (ABA) model or were used under control conditions (CTs). The data are shown as mean ± SEM and were analyzed using two-way ANOVA (TLR4 IEC −/− × ABA). The two-way ANOVA significance ( p < 0.05 or ABA, TLR4 IEC −/− and/or Int for interaction) is indicated by bold and underlined font. Tukey's multiple comparisons test results are indicated as * p < 0.05, *** p < 0.001. n and exact p- value on Figure S10.

Article Snippet: Gut peptides regulating metabolism and food intake, GLP1 and PYY (Phoenix Pharmaceuticals, Karlsruhe, Germany), corticosterone (Abnova, KA0468, VWR international SAS, Fontenay-sous-Bois, France), estradiol E2 (Cusabio, CSB-E05109m), and progesterone (antibodies online, ABIN6969565) were measured by enzyme immunoassays in plasma samples ( ).

Techniques: Concentration Assay, Activity Assay, Control