Obeticholic acid improves adipose morphometry and inflammation and reduces steatosis in dietary but not metabolic obesity in mice. Issue 1 (2nd November 2016)

• Record Type: Journal Article
• Authors: Haczeyni, Fahrettin; Poekes, Laurence; Wang, Hans; Mridha, Auvro R.; Barn, Vanessa; Geoffrey Haigh, W.; Ioannou, George N.; Yeh, Matthew M.; Leclercq, Isabelle A.; Teoh, Narcissus C.; Farrell, Geoffrey C.
• Is Part Of: Obesity. Volume 25:Issue 1(2017)
• Page Start: 155
• Page End: 165
• Publication Date: 2016-11-02
• Subjects: Obesity -- Periodicals; 616.398005
• DOI: 10.1002/oby.21701
• Languages: English
• ISSNs: 1930-7381

Abstract

Abstract : Objective: Nonalcoholic steatohepatitis (NASH) is the outcome of interactions between overnutrition, energy metabolism, and adipose function. Obeticholic acid (OCA) improves steatosis in patients but for unknown reasons does not resolve NASH pathology. This study therefore investigated OCA effects in Wt mice, which develop obesity with atherogenic dietary feeding, and appetite‐dysregulated, Alms1 mutant foz/foz mice fed the same diet, which develop metabolic obesity and diabetes. Methods: OCA (1 mg/kg) was administered orally to female foz/foz mice and Wt littermates from weaning until 28 weeks. Adipose indices, glucose tolerance, and fatty liver pathology were studied. Experiments were repeated with OCA 10 mg/kg. Results: OCA reduced body weight and hepatic lipids and improved glucose disposal only in Wt mice. OCA limited Wt adipose expansion, altered morphometry in favor of small adipocytes, enhanced expression of genes indicating adipose browning, and reduced crown‐like structure number in visceral adipose tissue. foz/foz mice showed more crown‐like structures in all compartments; OCA failed to alter adipose morphometry, browning, inflammation, or improve NASH severity, even at 10 mg/kg. Conclusions: OCA improved adipose indices, glucose tolerance, and steatosis in a milder metabolic phenotype but failed to improve these factors in morbidly obese diabetic mice. These results help explain OCA's limited efficacy to reverse human NASH.