General Information:
Id: | 904 (click here to show other Interactions for entry) |
Diseases: |
Diabetes mellitus, type II
- [OMIM]
Fatty liver disease, nonalcoholic Insulin resistance |
Mus musculus | |
BAC-based transgenic Sirt1 mouse with moderate overexpression of Sirt1 | |
article | |
Reference: | Pfluger PT et al.(2008) Sirt1 protects against high-fat diet-induced metabolic damage Proc. Natl. Acad. Sci. U.S.A. 105: 9793-9798 [PMID: 18599449] |
Interaction Information:
Comment | Body weights and body lengths of 8- to 10-week-old transgenic Sirt1 mice did not differ from wild-type (WT) control mice on a standard diet (SD). Subsequent exposure for 19 weeks to a high-fat diet (HFD) did not lead to significant differences in body weight, fat mass, or lean mass, although a trend toward lower body weight and fat mass was observed in transgenic mice on HFD compared with WT controls. |
Formal Description Interaction-ID: 5370 |
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Comment | Neither plasma leptin levels nor adiponectin levels differed between genotypes on either SD or HFD. |
Formal Description Interaction-ID: 5373 |
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Comment | Neither plasma leptin levels nor adiponectin levels differed between genotypes on either SD or HFD. |
Formal Description Interaction-ID: 5374 |
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Comment | Transgenic Sirt1 mice exhibited increased food intake compared with wild-type mice on high-fat diet. |
Formal Description Interaction-ID: 5375 |
gene/protein affects_activity of phenotype |
Comment | Indirect calorimetry revealed that transgenic Sirt1 mice showed higher energy expenditure than wild-type mice on high-fat diet. No differences were observed in mice fed standard diet. |
Formal Description Interaction-ID: 5376 |
gene/protein affects_activity of phenotype |
Comment | Although Sirt1 transgenic mice present a modest increase in food intake under high-fat diet, this is compensated by a similarly modest increase in energy expenditure, thus indicating a balanced energy homeostasis. |
Formal Description Interaction-ID: 5379 |
gene/protein NOT affects_activity of process |
Comment | After 19 weeks of high-fat diet, wild-type mice presented with severe hepatosteatosis, including massive accumulation of large lipid droplets. Importantly, Sirt1 transgenic mice were almost entirely protected from NAFLD, showing a low number of lipid droplets with small diameters. |
Formal Description Interaction-ID: 5381 |
gene/protein affects_activity of disease Fatty liver disease, nonalcoholic |
Comment | In agreement with the observed Sirt1-mediated protection from hepatosteatosis, the authors found that Sirt1 transgenic mice presented lower levels of SREBP1c mRNA in response to high-fat diet. |
Formal Description Interaction-ID: 5382 |
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Comment | Sirt1 protects from NAFLD. |
Formal Description Interaction-ID: 5383 |
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Comment | Exposure to a high-fat diet and diet-induced obesity lead to a chronic inflammatory reaction, which is believed to be critical for the development of glucose intolerance and insulin resistance. The expression of IL-6 and TNF-alpha, two major proinflammatory cytokines, was significantly enhanced in livers of wild-type mice on a chronic high-fat diet (HFD). Transgenic mice on HFD, however, still exhibited low levels of inflammatory markers, comparable to those seen in wild-type and transgenic mice on chow diet. |
Formal Description Interaction-ID: 5388 |
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Drugbank entries | Show/Hide entries for IL6 |
Comment | Exposure to a high-fat diet and diet-induced obesity lead to a chronic inflammatory reaction, which is believed to be critical for the development of glucose intolerance and insulin resistance. The expression of IL-6 and TNF-alpha, two major proinflammatory cytokines, was significantly enhanced in livers of wild-type mice on a chronic high-fat diet (HFD). Transgenic mice on HFD, however, still exhibited low levels of inflammatory markers, comparable to those seen in wild-type and transgenic mice on chow diet. |
Formal Description Interaction-ID: 5389 |
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Drugbank entries | Show/Hide entries for TNF |
Comment | TNF-alpha stimulation resulted in significantly lower activation of NF-kappaB activation in Sirt1-transgenic cells (2.8-fold) compared with wild-type cells (5-fold). |
Formal Description Interaction-ID: 5394 |
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Comment | In addition to the reduced expression of inflammatory cytokines, the expression of the antioxidant proteins manganese superoxide dismutase (MnSOD) and the nuclear respiratory factor 1 (Nrf1), a master regulator in the protection from reactive oxygen species, were both increased in transgenic mice on both standard diet and high-fat diet, compared with wild-type mice. Both genes, MnSOD and Nrf1, have been demonstrated to be induced by PGC1alpha, which in turn is positively regulated by Sirt1. |
Formal Description Interaction-ID: 5396 |
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Drugbank entries | Show/Hide entries for SOD2 |
Comment | The overexpression of Sirt1 appears to protect transgenic mice from high-fat diet-induced hepatic inflammation through decreasing the NF-kappaB-mediated induction of inflammatory cytokines, as well as by the activation of antioxidant proteins, possibly mediated by PGC1alpha. |
Formal Description Interaction-ID: 5399 |
gene/protein decreases_activity of process |
Comment | Indirect calorimetry revealed that transgenic Sirt1 mice showed higher energy expenditure than wild-type mice on high-fat diet. No differences were observed in mice fed standard diet. |
Formal Description Interaction-ID: 13187 |
gene/protein NOT affects_activity of phenotype |
Comment | In addition to the reduced expression of inflammatory cytokines, the expression of the antioxidant proteins manganese superoxide dismutase (MnSOD) and the nuclear respiratory factor 1 (Nrf1), a master regulator in the protection from reactive oxygen species, were both increased in transgenic mice on both standard diet and high-fat diet, compared with wild-type mice. Both genes, MnSOD and Nrf1, have been demonstrated to be induced by PGC1alpha, which in turn is positively regulated by Sirt1. |
Formal Description Interaction-ID: 13191 |
|
Comment | In addition to the reduced expression of inflammatory cytokines, the expression of the antioxidant proteins manganese superoxide dismutase (MnSOD) and the nuclear respiratory factor 1 (Nrf1), a master regulator in the protection from reactive oxygen species, were both increased in transgenic mice on both standard diet and high-fat diet, compared with wild-type mice. Both genes, MnSOD and Nrf1, have been demonstrated to be induced by PGC1alpha, which in turn is positively regulated by Sirt1. |
Formal Description Interaction-ID: 13192 |
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Comment | The overexpression of Sirt1 appears to protect transgenic mice from high-fat diet-induced hepatic inflammation through decreasing the NF-kappaB-mediated induction of inflammatory cytokines, as well as by the activation of antioxidant proteins, possibly mediated by PGC1alpha. |
Formal Description Interaction-ID: 13193 |
gene/protein decreases_activity of process |