Changes in gene expression of cytochrome P-450 in liver, kidney and aorta of cirrhotic rats

• Published in: Prostaglandins & other lipid mediators Vol. 120; pp. 134 - 138
• Main Authors: Di Pascoli, Marco, Turato, Cristian, Zampieri, Francesca, Verardo, Alberto, Pontisso, Patrizia, Pesce, Paola, Sacerdoti, David, Bolognesi, Massimo
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.07.2015
• Subjects: Amides - pharmacology; Animals; Aorta - drug effects; Aorta - metabolism; Cytochrome P-450; Cytochrome P-450 Enzyme System - genetics; Epoxyeicosatrienoic acids; Gene Expression Regulation, Enzymologic - drug effects; Kidney - drug effects; Kidney - metabolism; Liver - drug effects; Liver - metabolism; Liver cirrhosis; Liver Cirrhosis - enzymology; Liver Cirrhosis - genetics; Male; Organ Specificity; Portal hypertension; Rats; Rats, Wistar; RNA, Messenger - genetics; RNA, Messenger - metabolism; Epoxyeicosatrienoic acids; Liver cirrhosis; Cytochrome P-450; Portal hypertension
• ISSN: 1098-8823
• DOI: 10.1016/j.prostaglandins.2015.03.009

Liver cirrhosis is characterized by structural and hemodynamic changes that affect mainly the liver, the kidney and the vascular system. Cytochrome P-450 (CYP) is a variegated family of enzymes that, among many other activities, metabolize arachidonic acid to the vasoactive epoxyeicosatrienoic acids (EETs). To investigate in an animal model of cirrhosis the m-RNA expression of CYPs in liver, kidney and aorta and to evaluate the effect of epoxygenase inhibition by N-(methylsulfonyl)-2-(2-propynyloxy)-benzenehexanamide (MS-PPOH). In aorta, liver and kidney from 3 control, 3 cirrhotic and 6 cirrhotic rats treated with MS-PPOH, quantitative real-time PCR reactions were performed and the m-RNA expression of CYP2J3, CYP2J4, CYP2J10, CYP2C11, CYP2C12 and CYP2C23 was calculated. In cirrhotic rats, the gene expression of hepatic CYP2C11 and CYP2J10 was increased, of aortic CYP2J4 was increased, of aortic CYP2C12 was reduced and of renal CYP2C11 was increased. In cirrhotic rats, MS-PPOH reduced CYP2J10 hepatic and CYP2C11 renal gene expression to levels similar to the ones of control rats. Changes in CYPs gene expression may contribute to the hemodynamic alterations typical of cirrhosis. The altered gene expression of CYPs can, in some cases, be reversed by epoxygenase inhibition.