Abstract
Cholestasis occurs in a wide variety of human liver diseases, and hepatocellular injury is an invariant feature of cholestasis causing liver dysfunction and inflammation, promoting fibrogenesis, and ultimately leading to liver failure. α-Melanocyte-stimulating hormone (α-MSH) is a potent anti-inflammatory agent in many models of inflammation, suggesting that it inhibits a critical step common to different forms of inflammation. The aim of this study was to investigate whether the gene transfer of α-MSH could attenuate hepatic inflammation after bile duct ligation in the rat. Studies were performed in bile duct-ligated (BDL) rats. Hydrodynamic-based gene transfection with α-MSH plasmid via rapid tail vein injection was performed 30 min after ligation of bile duct. The endpoints were studied as markers of inflammation 7 days after bile duct ligation. α-MSH expression in liver via a single administration of naked plasmid was demonstrated. Liver inflammation index, including neutrophil infiltration and serum alanine aminotransferase, were significantly reduced in α-MSH gene transfer rats. Markers for liver inflammation, including expression of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and inducible NO synthase (iNOS) mRNA, as assessed by real-time PCR, were also attenuated by α-MSH gene therapy. Expression of iNOS protein in liver diminished after α-MSH gene transfer. Consistent with these data, hepatic stellate cells (HSC) and Kupffer cells were markedly inhibited in α-MSH gene-treated rats. Our findings show that gene transfer of α-MSH could attenuate hepatic inflammation after bile duct ligation in the rat.
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This work was supported by Topnotch Stroke Research Center Grant, Ministry of Education, and Department of Health (Grant No. DOH-TD-B-111-002), Taiwan
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Wang, CC., Lin, JW., Lee, LM. et al. α-Melanocyte-Stimulating Hormone Gene Transfer Attenuates Inflammation after Bile Duct Ligation in the Rat. Dig Dis Sci 53, 556–563 (2008). https://doi.org/10.1007/s10620-007-9901-6
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DOI: https://doi.org/10.1007/s10620-007-9901-6