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L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell

BACKGROUND AND AIMS: Recent studies have shown that activated pancreatic stellate cells (PSCs) play a major role in pancreatic fibrogenesis. We aimed to study the effect of L-cysteine administration on fibrosis in chronic pancreatitis (CP) induced by trinitrobenzene sulfonic acid (TNBS) in rats and...

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Autores principales: Yang, LiJuan, Shen, JiaQing, He, ShanShan, Hu, GuoYong, Shen, Jie, Wang, Feng, Xu, Ling, Dai, WeiQi, Xiong, Jie, Ni, JianBo, Guo, ChuanYong, Wan, Rong, Wang, XingPeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281011/
https://www.ncbi.nlm.nih.gov/pubmed/22359633
http://dx.doi.org/10.1371/journal.pone.0031807
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author Yang, LiJuan
Shen, JiaQing
He, ShanShan
Hu, GuoYong
Shen, Jie
Wang, Feng
Xu, Ling
Dai, WeiQi
Xiong, Jie
Ni, JianBo
Guo, ChuanYong
Wan, Rong
Wang, XingPeng
author_facet Yang, LiJuan
Shen, JiaQing
He, ShanShan
Hu, GuoYong
Shen, Jie
Wang, Feng
Xu, Ling
Dai, WeiQi
Xiong, Jie
Ni, JianBo
Guo, ChuanYong
Wan, Rong
Wang, XingPeng
author_sort Yang, LiJuan
collection PubMed
description BACKGROUND AND AIMS: Recent studies have shown that activated pancreatic stellate cells (PSCs) play a major role in pancreatic fibrogenesis. We aimed to study the effect of L-cysteine administration on fibrosis in chronic pancreatitis (CP) induced by trinitrobenzene sulfonic acid (TNBS) in rats and on the function of cultured PSCs. METHODS: CP was induced by TNBS infusion into rat pancreatic ducts. L-cysteine was administrated for the duration of the experiment. Histological analysis and the contents of hydroxyproline were used to evaluate pancreatic damage and fibrosis. Immunohistochemical analysis of α-SMA in the pancreas was performed to detect the activation of PSCs in vivo. The collagen deposition related proteins and cytokines were determined by western blot analysis. DNA synthesis of cultured PSCs was evaluated by BrdU incorporation. We also evaluated the effect of L-cysteine on the cell cycle and cell activation by flow cytometry and immunocytochemistry. The expression of PDGFRβ, TGFβRII, collagen 1α1 and α-SMA of PSCs treated with different concentrations of L-cysteine was determined by western blot. Parameters of oxidant stress were evaluated in vitro and in vivo. Nrf2, NQO1, HO-1, IL-1β expression were evaluated in pancreas tissues by qRT-PCR. RESULTS: The inhibition of pancreatic fibrosis by L-cysteine was confirmed by histological observation and hydroxyproline assay. α-SMA, TIMP1, IL-1β and TGF-β1 production decreased compared with the untreated group along with an increase in MMP2 production. L-cysteine suppressed the proliferation and extracellular matrix production of PSCs through down-regulating of PDGFRβ and TGFβRII. Concentrations of MDA+4-HNE were decreased by L-cysteine administration along with an increase in GSH levels both in tissues and cells. In addition, L-cysteine increased the mRNA expression of Nrf2, NQO1 and HO-1 and reduced the expression of IL-1β in L-cysteine treated group when compared with control group. CONCLUSION: L-cysteine treatment attenuated pancreatic fibrosis in chronic pancreatitis in rats.
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spelling pubmed-32810112012-02-22 L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell Yang, LiJuan Shen, JiaQing He, ShanShan Hu, GuoYong Shen, Jie Wang, Feng Xu, Ling Dai, WeiQi Xiong, Jie Ni, JianBo Guo, ChuanYong Wan, Rong Wang, XingPeng PLoS One Research Article BACKGROUND AND AIMS: Recent studies have shown that activated pancreatic stellate cells (PSCs) play a major role in pancreatic fibrogenesis. We aimed to study the effect of L-cysteine administration on fibrosis in chronic pancreatitis (CP) induced by trinitrobenzene sulfonic acid (TNBS) in rats and on the function of cultured PSCs. METHODS: CP was induced by TNBS infusion into rat pancreatic ducts. L-cysteine was administrated for the duration of the experiment. Histological analysis and the contents of hydroxyproline were used to evaluate pancreatic damage and fibrosis. Immunohistochemical analysis of α-SMA in the pancreas was performed to detect the activation of PSCs in vivo. The collagen deposition related proteins and cytokines were determined by western blot analysis. DNA synthesis of cultured PSCs was evaluated by BrdU incorporation. We also evaluated the effect of L-cysteine on the cell cycle and cell activation by flow cytometry and immunocytochemistry. The expression of PDGFRβ, TGFβRII, collagen 1α1 and α-SMA of PSCs treated with different concentrations of L-cysteine was determined by western blot. Parameters of oxidant stress were evaluated in vitro and in vivo. Nrf2, NQO1, HO-1, IL-1β expression were evaluated in pancreas tissues by qRT-PCR. RESULTS: The inhibition of pancreatic fibrosis by L-cysteine was confirmed by histological observation and hydroxyproline assay. α-SMA, TIMP1, IL-1β and TGF-β1 production decreased compared with the untreated group along with an increase in MMP2 production. L-cysteine suppressed the proliferation and extracellular matrix production of PSCs through down-regulating of PDGFRβ and TGFβRII. Concentrations of MDA+4-HNE were decreased by L-cysteine administration along with an increase in GSH levels both in tissues and cells. In addition, L-cysteine increased the mRNA expression of Nrf2, NQO1 and HO-1 and reduced the expression of IL-1β in L-cysteine treated group when compared with control group. CONCLUSION: L-cysteine treatment attenuated pancreatic fibrosis in chronic pancreatitis in rats. Public Library of Science 2012-02-16 /pmc/articles/PMC3281011/ /pubmed/22359633 http://dx.doi.org/10.1371/journal.pone.0031807 Text en Yang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yang, LiJuan
Shen, JiaQing
He, ShanShan
Hu, GuoYong
Shen, Jie
Wang, Feng
Xu, Ling
Dai, WeiQi
Xiong, Jie
Ni, JianBo
Guo, ChuanYong
Wan, Rong
Wang, XingPeng
L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell
title L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell
title_full L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell
title_fullStr L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell
title_full_unstemmed L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell
title_short L-Cysteine Administration Attenuates Pancreatic Fibrosis Induced by TNBS in Rats by Inhibiting the Activation of Pancreatic Stellate Cell
title_sort l-cysteine administration attenuates pancreatic fibrosis induced by tnbs in rats by inhibiting the activation of pancreatic stellate cell
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281011/
https://www.ncbi.nlm.nih.gov/pubmed/22359633
http://dx.doi.org/10.1371/journal.pone.0031807
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