Biliary secretion of S-nitrosoglutathione is involved in the hypercholeresis induced by ursodeoxycholic acid in the normal rat

Authors

  • Carlos M. Rodríguez-Ortigosa,

    Corresponding author
    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
    2. CIBERehd, Pamplona, Spain
    • Division of Hepatology and Gene Therapy, CIMA University of Navarra, Avda. Pio XII, 55 (31008) Pamplona, Spain
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    • fax: +34 948 194717

  • Jesús M. Banales,

    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
    2. CIBERehd, Pamplona, Spain
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  • Israel Olivas,

    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
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  • Iker Uriarte,

    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
    2. CIBERehd, Pamplona, Spain
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  • José J.G. Marín,

    1. Laboratory of Experimental Hepatology and Drug Targeting, University of Salamanca, Salamanca, Spain
    2. CIBERehd, Salamanca, Spain
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  • Fernando J. Corrales,

    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
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  • Juan F. Medina,

    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
    2. CIBERehd, Pamplona, Spain
    3. Liver Unit, University of Navarra Clinic, Pamplona, Spain
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  • Jesús Prieto

    Corresponding author
    1. Division of Hepatology and Gene Therapy, CIMA University of Navarra, Pamplona, Spain
    2. CIBERehd, Pamplona, Spain
    3. Liver Unit, University of Navarra Clinic, Pamplona, Spain
    • Liver Unit, University of Navarra Clinic, Avda. Pio XII, 36 (31008) Pamplona, Spain
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    • fax: +34 948 296500


  • Potential conflict of interest: Nothing to report.

Abstract

Ursodeoxycholic acid (UDCA) induces bicarbonate-rich hypercholeresis by incompletely defined mechanisms that involve the stimulation of adenosine triphosphate (ATP) release from cholangiocytes. As nitric oxide (NO) at a low concentration can stimulate a variety of secretory processes, we investigated whether this mediator could be implicated in the choleretic response to UDCA. Our in vivo experiments with the in situ perfused rat liver model in anesthetized rats, showed that UDCA infusion increased the biliary secretion of NO derivatives, hepatic inducible NO synthase expression, and NO synthase activity in liver tissue. UDCA also stimulated NO release by isolated rat hepatocytes. In contrast to UDCA, cholic acid was a poor inducer of NO secretion, and tauroursodeoxycholic acid showed no effect on NO secretion. Upon UDCA administration, NO was found in bile as low-molecular-weight nitrosothiols, of which S-nitrosoglutathione (GSNO) was the predominant species. UDCA-stimulated biliary NO secretion was abolished by the inhibition of inducible NO synthase with Nω-nitro-L-arginine methyl ester in isolated perfused livers and also in rats whose livers were depleted of glutathione with buthionine sulfoximine. Moreover, the biliary secretion of NO species was significantly diminished in UDCA-infused transport mutant [ATP–binding cassette C2 (ABCC2)/multidrug resistance–associated protein 2 (Mrp2)–deficient] rats, and this finding was consistent with the involvement of the glutathione carrier ABCC2/Mrp2 in the canalicular transport of GSNO. It was particularly noteworthy that in cultured normal rat cholangiocytes, GSNO activated protein kinase B, protected against apoptosis, and enhanced UDCA-induced ATP release to the medium; this effect was blocked by phosphoinositide 3-kinase inhibition. Finally, retrograde GSNO infusion into the common bile duct increased bile flow and biliary bicarbonate secretion. Conclusion: UDCA induces biliary secretion of GSNO, which contributes to stimulating ductal secretion. (HEPATOLOGY 2010;)

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