| First Author | Holter MM | Year | 2020 |
| Journal | Nutrients | Volume | 12 |
| Issue | 7 | PubMed ID | 32708970 |
| Mgi Jnum | J:294231 | Mgi Id | MGI:6455113 |
| Doi | 10.3390/nu12072124 | Citation | Holter MM, et al. (2020) Compound 18 Improves Glucose Tolerance in a Hepatocyte TGR5-dependent Manner in Mice. Nutrients 12(7) |
| abstractText | The bile acid receptor, TGR5, is a key regulator of glucose homeostasis, but the mechanisms by which TGR5 signaling improves glucose regulation are incompletely defined. In particular, TGR5 has an increasingly appreciated role in liver physiology and pathobiology; however, whether TGR5 signaling within the liver contributes to its glucoregulatory effects is unknown. Therefore, we investigated the role of hepatocyte TGR5 signaling on glucose regulation using a hepatocyte-specific TGR5 knockout mouse model. Hepatocyte-specific Tgr5(Hep+/+) and Tgr5(Hep-/-) mice were fed a high fat diet (HFD) for 7 weeks and then orally gavaged with three doses of a highly potent, TGR5-specific agonist, Compound 18 (10 mg/kg), or vehicle, over 72 h and underwent an oral glucose tolerance test (OGTT) after the last dose. Herein, we report that TGR5 mRNA and protein is present in mouse hepatocytes. Cumulative food intake, body weight, and adiposity do not differ between Tgr5(Hep+/+) and Tgr5(Hep-/-) mice with or without treatment with Compound 18. However, administration of Compound 18 improves glucose tolerance in Tgr5(HEP+/+) mice, but not in Tgr5(Hep-/-) mice. Further, this effect occurred independent of body weight and GLP-1 secretion. Together, these data demonstrate that TGR5 is expressed in hepatocytes, where it functions as a key regulator of whole-body glucose homeostasis. |
