Literature DB >> 22117825

The hepatic protective mechanism of Ginkgo biloba extract in rats with obstructive jaundice.

Ming-Zhe Weng1, Xian-Ping Zhou, Jian-Guang Jia, Jing Ding, Cui-Fu Fang, Yi-Yu Qin, Shao-Fu Tao, Long-Hua Rao, Ji-Yu Li, Zhi-Wei Quan.   

Abstract

The objective of our study was to examine the hepatic protective mechanism of Ginkgo biloba extract (GBE) in rats with obstructive jaundice (OJ). Twenty rats underwent bile duct ligation and received daily intraperitoneal injections of either control saline or Ginkgo biloba extract for 14 days. Ten sham-operated rats had their bile duct exposed but not ligated or sectioned. Serum alanine transaminase (ALT) was analyzed for liver function tests and liver damage was further assessed by histologic examination. The levels of endothelin 1 (ET-1) and nitric oxide (NO) in blood and liver homogenate were measured. The serum alanine transaminase was elevated in the bile duct ligation rats (BDL rats); GBE could significantly lower serum transaminase level and ameliorate liver histological damage. ET-1 and NO levels in both plasma and liver tissue were also elevated in common bile duct (CBD)-ligated rats, but this increase was significantly decreased by GBE treatment. Moreover, the degree of liver damage severity positively correlates with high levels of ET-1 and NO. GBE mediated the liver protective effect at least in part by suppressing overproduction of ET-1 and NO and restoring a proper balance between ET-1 and NO to some extent.

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Year:  2011        PMID: 22117825      PMCID: PMC4362573          DOI: 10.17305/bjbms.2011.2547

Source DB:  PubMed          Journal:  Bosn J Basic Med Sci        ISSN: 1512-8601            Impact factor:   3.363


  20 in total

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2.  Regulation of inducible nitric oxide synthase in hepatic sinusoidal endothelial cells.

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10.  Characterization of 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate synthase (HDS) gene from Ginkgo biloba.

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4.  Ginkgo biloba extract (EGb761) did not express estrogenic activity in an immature rat uterotrophic assay.

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