Additive Inhibitory Effect of Experimentally Induced Hepatic Cirrhosis by Agonists of Peroxisome Proliferator Activator Receptor gamma and Retinoic Acid Receptor

作者：Bruck Rafael^*; Weiss Sigal; Aeed Hussein; Pines Mark; Halpern Zamir; Zvibel Isabel

来源：Digestive Diseases and Sciences, 2009, 54(2): 292-299.

DOI：10.1007/s10620-008-0336-5

• Hepatic stellate cells
• Peroxisome proliferator activator receptors
• All-trans retinoic acid
• Thioacetamide
• Liver fibrosis

Peroxisome proliferator activator receptor (PPAR) ligands prevent liver fibrosis, while the role of all-trans retinoic acid (ATRA) and its metabolite 9-cis retinoic acid (9-cis RA) is less clear. We have investigated the ability of the combination of PPAR gamma ligand rosiglitazone (RSG) and of ATRA to prevent liver fibrosis. In vivo treatment with RSG or ATRA reduced fibrotic nodules, spleen weight, and hydroxyproline levels in rat model of thioacetamide-induced liver fibrosis. The combination of ATRA + RSG caused the strongest inhibition, accompanied by decreased expression of collagen I, alpha-smooth muscle actin, TGF beta 1, and TNF alpha. In vitro studies showed that PPAR gamma ligand 15-deoxy-Delta 12,14- prostaglandinJ(2)[PJ(2)] and RXR ligand 9-cis RA or PJ(2) and ATRA inhibited proliferation of hepatic stellate cells HSC-T6. 9-cis RA inhibited c-jun levels and also inhibited expression of its receptor RXR alpha in HSC-T6 cells. The combination of PPAR-gamma and RAR agonists demonstrated an additive effect in the inhibition of TAA-induced hepatic fibrosis, due to inhibition of HSC proliferation and reduction of profibrotic TGFb1 and proinflammatory TNF alpha.

• 出版日期2009-2