PMID- 21286345 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20110714 LR - 20211020 IS - 1936-0541 (Electronic) IS - 1936-0533 (Print) IS - 1936-0533 (Linking) VI - 4 IP - 4 DP - 2010 Aug 12 TI - Effects of nuclear receptor FXR on the regulation of liver lipid metabolism in patients with non-alcoholic fatty liver disease. PG - 741-8 LID - 10.1007/s12072-010-9202-6 [doi] AB - OBJECTIVE: The aim of this study was to explore the role of farnesoid X receptor (FXR) in liver lipid metabolism of non-alcoholic fatty liver disease (NAFLD) patients. METHODS: In this study, pathology and clinical criteria confirmed NAFLD in patients. Fatty acid synthetase (FAS)-positive liver cells were visualized by laser scanning confocal microscopy. Levels of FXR, liver X receptor (LXR), sterol regulatory element binding protein 1C (SREBP-1C), and small heterodimer partner (SHP) proteins were detected by Western blot. FXR, LXR, and SHP mRNA levels were measured by real-time PCR. RESULTS: In patients with NAFLD, a significant positive relationship between the degree of hepatic steatosis and serum triglycerides and cholesterol (correlation coefficient > 0.5, P < 0.05) was seen. The NAFLD patients had more FAS protein in liver, which suggests that there could have been more of fatty acid synthesis in hepatic cells (P < 0.05). The levels of FXR protein and mRNA were decreased in patients with NAFLD (P < 0.05), while those of LXR and SREBP-1C were increased (P < 0.05). The levels of SREBP-1C positively correlated with the degree of hepatic steatosis. There were no differences between the levels of SHP protein and mRNA both in NAFLD patients and normal controls (P > 0.05). CONCLUSION: Our data showed that the decreased expression of hepatic FXR is associated with an increased expression of LXR, SREBP-1C, and hepatic triglyceride synthesis; furthermore, increased SREBP-1C is associated with the degree of hepatic steatosis in the NAFLD patients. FAU - Yang, Zhao-Xia AU - Yang ZX FAU - Shen, Wei AU - Shen W FAU - Sun, Hang AU - Sun H LA - eng PT - Journal Article DEP - 20100812 PL - United States TA - Hepatol Int JT - Hepatology international JID - 101304009 PMC - PMC2994619 OTO - NOTNLM OT - FXR OT - Human OT - Lipid metabolism OT - NAFLD EDAT- 2011/02/03 06:00 MHDA- 2011/02/03 06:01 PMCR- 2010/08/12 CRDT- 2011/02/03 06:00 PHST- 2010/01/29 00:00 [received] PHST- 2010/07/12 00:00 [accepted] PHST- 2011/02/03 06:00 [entrez] PHST- 2011/02/03 06:00 [pubmed] PHST- 2011/02/03 06:01 [medline] PHST- 2010/08/12 00:00 [pmc-release] AID - 9202 [pii] AID - 10.1007/s12072-010-9202-6 [doi] PST - epublish SO - Hepatol Int. 2010 Aug 12;4(4):741-8. doi: 10.1007/s12072-010-9202-6.