| First Author | Frieler RA | Year | 2022 |
| Journal | Obesity (Silver Spring) | Volume | 30 |
| Issue | 9 | Pages | 1818-1830 |
| PubMed ID | 35927796 | Mgi Jnum | J:333764 |
| Mgi Id | MGI:7440145 | Doi | 10.1002/oby.23509 |
| Citation | Frieler RA, et al. (2022) Aconitate decarboxylase 1 regulates glucose homeostasis and obesity in mice. Obesity (Silver Spring) 30(9):1818-1830 |
| abstractText | OBJECTIVE: The intersection between immunology and metabolism contributes to the pathogenesis of obesity-associated metabolic diseases as well as molecular control of inflammatory responses. The metabolite itaconate and the cell-permeable derivatives have robust anti-inflammatory effects; therefore, it is hypothesized that cis-aconitate decarboxylase (Acod1)-produced itaconate has a protective, anti-inflammatory effect during diet-induced obesity and metabolic disease. METHODS: Wild-type and Acod1(-/-) mice were subjected to diet-induced obesity. Glucose metabolism was analyzed by glucose tolerance tests, insulin tolerance tests, and indirect calorimetry. Gene expression and transcriptome analysis was performed using quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and RNA sequencing. RESULTS: Wild-type and Acod1(-/-) mice on high-fat diet had equivalent weight gain, but Acod1(-/-) mice had impaired glucose metabolism. Insulin tolerance tests and glucose tolerance tests after 12 weeks on high-fat diet revealed significantly higher blood glucose levels in Acod1(-/-) mice. This was associated with significant enrichment of inflammatory gene sets and a reduction in genes related to adipogenesis and fatty acid metabolism. Analysis of naive Acod1(-/-) mice showed a significant increase in fat deposition at 3 and 6 months of age and obesity and insulin resistance by 12 months. CONCLUSIONS: The data show that Acod1 has an important role in the regulation of glucose homeostasis and obesity under normal and high-fat diet conditions. |
