PMID- 31632109 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230519 IS - 1178-7007 (Print) IS - 1178-7007 (Electronic) IS - 1178-7007 (Linking) VI - 12 DP - 2019 TI - Plant-derived oleanolic acid ameliorates markers associated with non-alcoholic fatty liver disease in a diet-induced pre-diabetes rat model. PG - 1953-1962 LID - 10.2147/DMSO.S218626 [doi] AB - BACKGROUND: The increased prevalence of non-alcoholic fatty liver disease (NAFLD) in type 2 diabetes mellitus (T2DM) patients is becoming a worldwide health burden. Studies have indicated, however, that the onset of NAFLD occurs during pre-diabetes, a condition that often precedes the onset of T2DM. Oleanolic acid has been reported to improve glucose homeostasis in diet-induced pre-diabetes; however, the effects of this triterpene on liver function have not been evaluated. PURPOSE: This study was aimed at evaluating the therapeutic effects of oleanolic acid (OA) on selected markers of NAFLD in a pre-diabetes rat model. METHODS AND MATERIALS: Pre-diabetes was induced by exposing Sprague Dawley rats to a high-fat high-carbohydrate diet for 20 weeks. The pre-diabetic rats were then treated with OA (80 mg/kg) or metformin (500 mg/kg) in the presence and absence of dietary interventions for a period of 12 weeks. The effects of OA were evaluated on parameters including plasma triglycerides (TGs), very low-density lipoprotein (VLDL) particles, bilirubin, AST, ALT, SREBP and antioxidant profile while the livers were collected for histological analysis. RESULTS: The findings of this study showed that the administration of OA to pre-diabetic rats ameliorated body/liver weights ratio and significantly decreased plasma triglycerides (TGs) and VLDL. Furthermore, OA also ameliorated hepatic oxidative stress, lowered the SREBP expression and intrahepatic TGs. In addition, OA administration decreased plasma concentrations of bilirubin and liver damage enzyme biomarkers. CONCLUSION: The findings of the study suggest that OA ameliorates the risk of developing pre-diabetes-related NAFLD through the prevention of intrahepatic fat accumulation while also lowering hepatic inflammation. CI - (c) 2019 Gamede et al. FAU - Gamede, Mlindeli AU - Gamede M AUID- ORCID: 0000-0001-5512-1545 AD - School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa. FAU - Mabuza, Lindokuhle AU - Mabuza L AD - School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa. FAU - Ngubane, Phikelelani AU - Ngubane P AUID- ORCID: 0000-0003-2150-1149 AD - School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa. FAU - Khathi, Andile AU - Khathi A AD - School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa. LA - eng PT - Journal Article DEP - 20191001 PL - New Zealand TA - Diabetes Metab Syndr Obes JT - Diabetes, metabolic syndrome and obesity : targets and therapy JID - 101515585 PMC - PMC6778448 OTO - NOTNLM OT - NAFLD and oleanolic acid OT - insulin resistance OT - pre-diabetes COIS- The authors report no conflict of interest in this work. EDAT- 2019/10/22 06:00 MHDA- 2019/10/22 06:01 PMCR- 2019/10/01 CRDT- 2019/10/22 06:00 PHST- 2019/06/07 00:00 [received] PHST- 2019/07/24 00:00 [accepted] PHST- 2019/10/22 06:00 [entrez] PHST- 2019/10/22 06:00 [pubmed] PHST- 2019/10/22 06:01 [medline] PHST- 2019/10/01 00:00 [pmc-release] AID - 218626 [pii] AID - 10.2147/DMSO.S218626 [doi] PST - epublish SO - Diabetes Metab Syndr Obes. 2019 Oct 1;12:1953-1962. doi: 10.2147/DMSO.S218626. eCollection 2019.