General Information:
Id: | 7,511 |
Diseases: |
Diabetes mellitus, type II
- [OMIM]
Inflammatory bowel disease Insulin resistance |
Mus musculus | |
article | |
Reference: | Arsenescu R et al.(2011) Role of the xenobiotic receptor in inflammatory bowel disease Inflamm. Bowel Dis. 17: 1149-1162 [PMID: 20878756] |
Interaction Information:
Comment | AhR-/- mice died before the end of the treatment. However, AhR-/+ mice exhibited decreased disease activity compared to WT mice. The AhR-/+ mice expressed less proinflammatory cytokines such as tumor necrosis factor alpha (TNF-alpha) and IL17 and increased antiinflammatory IL-10 compared with the AhR+/+ mice in the colon. |
Formal Description Interaction-ID: 74107 |
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Drugbank entries | Show/Hide entries for AHR or TNF |
Comment | AhR-/- mice died before the end of the treatment. However, AhR-/+ mice exhibited decreased disease activity compared to WT mice. The AhR-/+ mice expressed less proinflammatory cytokines such as tumor necrosis factor alpha (TNF-alpha) and IL17 and increased antiinflammatory IL-10 compared with the AhR+/+ mice in the colon. |
Formal Description Interaction-ID: 74109 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | AhR-/- mice died before the end of the treatment. However, AhR-/+ mice exhibited decreased disease activity compared to WT mice. The AhR-/+ mice expressed less proinflammatory cytokines such as tumor necrosis factor alpha (TNF-alpha) and IL17 and increased antiinflammatory IL-10 compared with the AhR+/+ mice in the colon. |
Formal Description Interaction-ID: 74110 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | AhR-/- mice died before the end of the treatment. However, AhR-/+ mice exhibited decreased disease activity compared to WT mice. The AhR-/+ mice expressed less proinflammatory cytokines such as tumor necrosis factor alpha (TNF-alpha) and IL17 and increased antiinflammatory IL-10 compared with the AhR+/+ mice in the colon. |
Formal Description Interaction-ID: 74111 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | Colonic macrophage infiltration was attenuated in the AhR-/+ group. |
Formal Description Interaction-ID: 74112 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | Adiponectin, the only known anti-inflammatory adipokine, is considered an exclusive product of adipose tissue. The study shows that adiponectin gene is also expressed in the colon. |
Formal Description Interaction-ID: 74116 |
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Comment | AhR-/+ mice treated with DSS presented a significant downregulation of the only known precursor of angiotensin I/II - angiotensinogen, as well as the angiotensin converting enzyme ACE, and angiotensin receptor AT1 gene expression compared to the WT group. Importantly, the AhR-/+ mice presented significant less AT1 mRNA gene expression under basal conditions. Compared to WT mice with colitis, the immunohistochemistry of colon sections of AhR-/+ mice with colitis revealed decreased angiotensin II, AT1 receptor and ACE expression. |
Formal Description Interaction-ID: 74117 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | AhR-/+ mice treated with DSS presented a significant downregulation of the only known precursor of angiotensin I/II - angiotensinogen, as well as the angiotensin converting enzyme ACE, and angiotensin receptor AT1 gene expression compared to the WT group. Importantly, the AhR-/+ mice presented significant less AT1 mRNA gene expression under basal conditions. Compared to WT mice with colitis, the immunohistochemistry of colon sections of AhR-/+ mice with colitis revealed decreased angiotensin II, AT1 receptor and ACE expression. |
Formal Description Interaction-ID: 74118 |
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Drugbank entries | Show/Hide entries for AHR or ACE |
Comment | AhR-/+ mice treated with DSS presented a significant downregulation of the only known precursor of angiotensin I/II - angiotensinogen, as well as the angiotensin converting enzyme ACE, and angiotensin receptor AT1 gene expression compared to the WT group. Importantly, the AhR-/+ mice presented significant less AT1 mRNA gene expression under basal conditions. Compared to WT mice with colitis, the immunohistochemistry of colon sections of AhR-/+ mice with colitis revealed decreased angiotensin II, AT1 receptor and ACE expression. |
Formal Description Interaction-ID: 74119 |
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Drugbank entries | Show/Hide entries for AHR or AGTR1 |
Comment | All the AhR-/+ mice presented a higher basal adiponectin mRNA gene expression that did not change during treatment. |
Formal Description Interaction-ID: 74120 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | Adiponectin mRNA gene expression dropped significantly in the wild type mice during colitis. Consequently, adiponectin receptors (AdipoQ R1 and R2) were downregulated during DSS colitis in all groups. |
Formal Description Interaction-ID: 74122 |
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Comment | Adiponectin mRNA gene expression dropped significantly in the wild type mice during colitis. Consequently, adiponectin receptors (AdipoQ R1 and R2) were downregulated during DSS colitis in all groups. |
Formal Description Interaction-ID: 74124 |
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Comment | Adiponectin mRNA gene expression dropped significantly in the wild type mice during colitis. Consequently, adiponectin receptors (AdipoQ R1 and R2) were downregulated during DSS colitis in all groups. |
Formal Description Interaction-ID: 74125 |
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Comment | T-Cadherin mRNA gene expression, a novel adiponectin receptor that serves to anchor adiponectin to cell surface, was upregulated only in the AhR-/+ mice and not in the WT mice with colitis. |
Formal Description Interaction-ID: 74126 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | AhR-/+ mice exposed to DSS had a lower expression of Protein of 44 kDa [Erp44] that inhibits the secretion of adiponectin oligomers from the endoplasmic reticulum [ER]. |
Formal Description Interaction-ID: 74129 |
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Comment | A significant downregulation of ER stress markers BIP and XBP1 was observed in the AhR-/+ mice exposed to DSS as compared to the WT mice with colitis. |
Formal Description Interaction-ID: 74131 |
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Drugbank entries | Show/Hide entries for AHR or HSPA5 |
Comment | A significant downregulation of ER stress markers BIP and XBP1 was observed in the AhR-/+ mice exposed to DSS as compared to the WT mice with colitis. |
Formal Description Interaction-ID: 74134 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | Since ER stress response is coupled to the cell death program, the mRNA expression of two pro-apoptotic molecules was investigated: C/EBP Homologous Protein [CHOP] and Caspase 12 [Casp12]. There was a significant downregulation of the expression of both pro-apoptotic genes only in the AhR-/+ mice exposed to DSS. |
Formal Description Interaction-ID: 74135 |
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Drugbank entries | Show/Hide entries for AHR |
Comment | Since ER stress response is coupled to the cell death program, the mRNA expression of two pro-apoptotic molecules was investigated: C/EBP Homologous Protein [CHOP] and Caspase 12 [Casp12]. There was a significant downregulation of the expression of both pro-apoptotic genes only in the AhR-/+ mice exposed to DSS. |
Formal Description Interaction-ID: 74136 |
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Drugbank entries | Show/Hide entries for AHR |