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Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats

BACKGROUND: Our aim was to study the effect of caffeic acid phenethyl ester (CAPE) on iNOS and cystathionine gamma-lyase (CSE) of hepatic fibrosis rat, and discuss the anti-hepatic fibrosis mechanism of caffeic acid phenethyl ester. MATERIAL/METHODS: We observed changes of NO and H(2)S in serum of h...

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Autores principales: Shi, Yan, Guo, Li, Shi, Lu, Yu, Jinyang, Song, Min, Li, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578650/
https://www.ncbi.nlm.nih.gov/pubmed/26378818
http://dx.doi.org/10.12659/MSM.895272
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author Shi, Yan
Guo, Li
Shi, Lu
Yu, Jinyang
Song, Min
Li, Yana
author_facet Shi, Yan
Guo, Li
Shi, Lu
Yu, Jinyang
Song, Min
Li, Yana
author_sort Shi, Yan
collection PubMed
description BACKGROUND: Our aim was to study the effect of caffeic acid phenethyl ester (CAPE) on iNOS and cystathionine gamma-lyase (CSE) of hepatic fibrosis rat, and discuss the anti-hepatic fibrosis mechanism of caffeic acid phenethyl ester. MATERIAL/METHODS: We observed changes of NO and H(2)S in serum of hepatic fibrosis rats. Enzyme-linked immunosorbent assay was used to test OD value of iNOS and CSE in serum of each. The expressions of iNOS and CSE protein in the liver were also detected by immunohistochemistry. RESULTS: Compared with the model group, the expression of NO and iNOS was decreased obviously and the level of H(2)S and CSE was increased in the CAPE group. CONCLUSIONS: CAPE has the effect of anti-hepatic fibrosis, which can be realized through adjusting the expression level of iNOS and CSE.
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spelling pubmed-45786502015-10-06 Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats Shi, Yan Guo, Li Shi, Lu Yu, Jinyang Song, Min Li, Yana Med Sci Monit Animal Study BACKGROUND: Our aim was to study the effect of caffeic acid phenethyl ester (CAPE) on iNOS and cystathionine gamma-lyase (CSE) of hepatic fibrosis rat, and discuss the anti-hepatic fibrosis mechanism of caffeic acid phenethyl ester. MATERIAL/METHODS: We observed changes of NO and H(2)S in serum of hepatic fibrosis rats. Enzyme-linked immunosorbent assay was used to test OD value of iNOS and CSE in serum of each. The expressions of iNOS and CSE protein in the liver were also detected by immunohistochemistry. RESULTS: Compared with the model group, the expression of NO and iNOS was decreased obviously and the level of H(2)S and CSE was increased in the CAPE group. CONCLUSIONS: CAPE has the effect of anti-hepatic fibrosis, which can be realized through adjusting the expression level of iNOS and CSE. International Scientific Literature, Inc. 2015-09-17 /pmc/articles/PMC4578650/ /pubmed/26378818 http://dx.doi.org/10.12659/MSM.895272 Text en © Med Sci Monit, 2015 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Animal Study
Shi, Yan
Guo, Li
Shi, Lu
Yu, Jinyang
Song, Min
Li, Yana
Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats
title Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats
title_full Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats
title_fullStr Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats
title_full_unstemmed Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats
title_short Caffeic Acid Phenethyl Ester inhibit Hepatic Fibrosis by Nitric Oxide Synthase and Cystathionine Gamma-Lyase in Rats
title_sort caffeic acid phenethyl ester inhibit hepatic fibrosis by nitric oxide synthase and cystathionine gamma-lyase in rats
topic Animal Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578650/
https://www.ncbi.nlm.nih.gov/pubmed/26378818
http://dx.doi.org/10.12659/MSM.895272
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