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Selective Liver Estrogen Receptor Modulation Prevents Steatosis, Diabetes, and Obesity Through the Anorectic Growth Differentiation Factor 15 Hepatokine in Mice
- Source :
- Hepatology Communications, Hepatology Communications, 2019, 3 (7), pp.908-924. ⟨10.1002/hep4.1363⟩, Hepatology Communications, Vol 3, Iss 7, Pp 908-924 (2019), Hepatology Communications 7 (3), 908-924. (2019)
- Publication Year :
- 2019
- Publisher :
- HAL CCSD, 2019.
-
Abstract
- Hepatocyte estrogen receptor alpha (ER alpha) was recently recognized as a relevant molecular target for nonalcoholic fatty liver disease (NAFLD) prevention. The present study defined to what extent hepatocyte ER alpha could be involved in preserving metabolic homeostasis in response to a full (17 beta-estradiol [E2]) or selective (selective estrogen receptor modulator [SERM]) activation. Ovariectomized mice harboring a hepatocyte-specific ER alpha deletion (LERKO mice) and their wild-type (WT) littermates were fed a high-fat diet (HFD) and concomitantly treated with E2, tamoxifen (TAM; the most used SERM), or vehicle. As expected, both E2 and TAM prevented all HFD-induced metabolic disorders in WT mice, and their protective effects against steatosis were abolished in LERKO mice. However, while E2 still prevented obesity and glucose intolerance in LERKO mice, hepatocyte ER alpha deletion also abrogated TAM-mediated control of food intake as well as its beneficial actions on adiposity, insulin sensitivity, and glucose homeostasis, suggesting a whole-body protective role for liver-derived circulating factors. Moreover, unlike E2, TAM induced a rise in plasma concentration of the anorectic hepatokine growth differentiation factor 15 (Gdf15) through a transcriptional mechanism dependent on hepatocyte ER alpha activation. Accordingly, ER alpha was associated with specific binding sites in the Gdf15 regulatory region in hepatocytes from TAM-treated mice but not under E2 treatment due to specific epigenetic modifications. Finally, all the protective effects of TAM were abolished in HFD-fed GDF15-knockout mice. Conclusion: We identified the selective modulation of hepatocyte ER alpha as a pharmacologic strategy to induce sufficient anorectic hepatokine Gdf15 to prevent experimental obesity, type 2 diabetes, and NAFLD.
Details
- Language :
- English
- ISSN :
- 2471254X
- Database :
- OpenAIRE
- Journal :
- Hepatology Communications, Hepatology Communications, 2019, 3 (7), pp.908-924. ⟨10.1002/hep4.1363⟩, Hepatology Communications, Vol 3, Iss 7, Pp 908-924 (2019), Hepatology Communications 7 (3), 908-924. (2019)
- Accession number :
- edsair.pmid.dedup....f21b6ea60ba1ee457f11a87588cc2f17