Literature DB >> 12791596

Polyphenols from Camellia sinenesis attenuate experimental cholestasis-induced liver fibrosis in rats.

Zhi Zhong1, Matthias Froh, Mark Lehnert, Robert Schoonhoven, Liu Yang, Henrik Lind, John J Lemasters, Ronald G Thurman.   

Abstract

Accumulation of hydrophobic bile acids during cholestasis leads to generation of oxygen free radicals in the liver. Accordingly, this study investigated whether polyphenols from green tea Camellia sinenesis, which are potent free radical scavengers, decrease hepatic injury caused by experimental cholestasis. Rats were fed a standard chow or a diet containing 0.1% polyphenolic extracts from C. sinenesis starting 3 days before bile duct ligation. After bile duct ligation, serum alanine transaminase increased to 760 U/l after 1 day in rats fed a control diet. Focal necrosis and bile duct proliferation were also observed after 1-2 days, and fibrosis developed 2-3 wk after bile duct ligation. Additionally, procollagen-alpha1(I) mRNA increased 30-fold 3 wk after bile duct ligation, accompanied by increased expression of alpha-smooth muscle actin and transforming growth factor-beta and the accumulation of 4-hydroxynenonal, an end product of lipid peroxidation. Polyphenol feeding blocked or blunted all of these bile duct ligation-dependent changes by 45-73%. Together, the results indicate that cholestasis due to bile duct ligation causes liver injury by mechanisms involving oxidative stress. Polyphenols from C. sinenesis scavenge oxygen radicals and prevent activation of stellate cells, thereby minimizing liver fibrosis.

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Year:  2003        PMID: 12791596     DOI: 10.1152/ajpgi.00008.2003

Source DB:  PubMed          Journal:  Am J Physiol Gastrointest Liver Physiol        ISSN: 0193-1857            Impact factor:   4.052


  24 in total

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2.  Aldehyde dehydrogenase-2 activation by Alda-1 decreases necrosis and fibrosis after bile duct ligation in mice.

Authors:  Hereward J Wimborne; Kenji Takemoto; Patrick M Woster; Don C Rockey; John J Lemasters; Zhi Zhong
Journal:  Free Radic Biol Med       Date:  2019-09-23       Impact factor: 7.376

3.  NIM811 (N-methyl-4-isoleucine cyclosporine), a mitochondrial permeability transition inhibitor, attenuates cholestatic liver injury but not fibrosis in mice.

Authors:  Hasibur Rehman; Venkat K Ramshesh; Tom P Theruvath; Insil Kim; Robert T Currin; Shailendra Giri; John J Lemasters; Zhi Zhong
Journal:  J Pharmacol Exp Ther       Date:  2008-09-18       Impact factor: 4.030

4.  Erdosteine treatment attenuates oxidative stress and fibrosis in experimental biliary obstruction.

Authors:  Göksel Sener; A Ozer Sehirli; Hale Z Toklu; Meral Yuksel; Feriha Ercan; Nursal Gedik
Journal:  Pediatr Surg Int       Date:  2007-01-10       Impact factor: 1.827

5.  The traditional ayurvedic medicine, Eugenia jambolana (Jamun fruit), decreases liver inflammation, injury and fibrosis during cholestasis.

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6.  Tannic acid inhibits cholangiocyte proliferation after bile duct ligation via a cyclic adenosine 5',3'-monophosphate-dependent pathway.

Authors:  Silvia Taffetani; Yoshiyuki Ueno; Fanyin Meng; Julie Venter; Heather Francis; Shannon Glaser; Gianfranco Alpini; Tushar Patel
Journal:  Am J Pathol       Date:  2005-06       Impact factor: 4.307

7.  Bile acids induce inflammatory genes in hepatocytes: a novel mechanism of inflammation during obstructive cholestasis.

Authors:  Katryn Allen; Hartmut Jaeschke; Bryan L Copple
Journal:  Am J Pathol       Date:  2010-12-23       Impact factor: 4.307

8.  Protective effect of Jasonia montana against ethinylestradiol-induced cholestasis in rats.

Authors:  Mohammed A Hussein; Soad M Abdel-Gawad
Journal:  Saudi Pharm J       Date:  2009-12-23       Impact factor: 4.330

9.  Antifibrotic effects of green tea on in vitro and in vivo models of liver fibrosis.

Authors:  Hye-Kyung Kim; Taik-Hoon Yang; Hong-Yon Cho
Journal:  World J Gastroenterol       Date:  2009-11-07       Impact factor: 5.742

10.  Beneficial Effects of Fermented Green Tea Extract in a Rat Model of Non-alcoholic Steatohepatitis.

Authors:  Kazuo Nakamoto; Fusako Takayama; Mitsumasa Mankura; Yuki Hidaka; Toru Egashira; Tetsuya Ogino; Hiromu Kawasaki; Akitane Mori
Journal:  J Clin Biochem Nutr       Date:  2009-04-25       Impact factor: 3.114

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