Protective Effect of Selenium-Enriched Green Tea on Carbon Tetrachloride-Induced Liver Fibrosis

The major pathogenic feature of liver fibrosis is that oxidative stress motivation of hepatic stellate cells (HSCs) alters the balance between the synthesis and degradation of extracellular matrix (ECM) and HSCs into proliferative myofibroblasts. Green tea and selenium (Se) can protect the liver fro...

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Veröffentlicht in:Biological trace element research 2022-05, Vol.200 (5), p.2233-2238
Hauptverfasser: Zhang, Lin, Xu, Jia-Ying, Wei, Yanyan, Gao, Shi-Lin, Wang, Lin, Zheng, Jia-Yang, Gu, Minghua, Qin, Li-Qiang
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container_issue 5
container_start_page 2233
container_title Biological trace element research
container_volume 200
creator Zhang, Lin
Xu, Jia-Ying
Wei, Yanyan
Gao, Shi-Lin
Wang, Lin
Zheng, Jia-Yang
Gu, Minghua
Qin, Li-Qiang
description The major pathogenic feature of liver fibrosis is that oxidative stress motivation of hepatic stellate cells (HSCs) alters the balance between the synthesis and degradation of extracellular matrix (ECM) and HSCs into proliferative myofibroblasts. Green tea and selenium (Se) can protect the liver from damage; however, the precise mechanism of green tea and the action of Se in green tea on hepatic fibrosis remain unclear. Several studies have demonstrated the profibrogenic role of 5-hydroxytryptamine (5-HT) and 5-hydroxytryptamine receptor (5-HTR) 2A/2B in the liver. The current study aimed to investigate the protective effects and possible mechanisms of selenium-enriched green tea on carbon tetrachloride (CCl 4 )-induced liver fibrosis in male C57BL/6 J mice. After a 4-week intervention with tea solution, histological analysis of the liver showed that green tea interventions alleviated hepatic fibrosis, which was supported by the changes in collagen type I, collagen type III, and α-smooth muscle actin in the liver. Tea interventions significantly inhibited the CCl 4 -provoked increase of duodenal 5-HT and tryptophan hydroxylase and hepatic 5-HT and 5-HTR2A/2B levels. All of them were lower in the selenium-enriched green tea group than in regular green tea group. Se-enriched green tea had a more pronounced improvement in liver ECM deposition and scar formation and peripheral 5-HT signals than regular green tea. Thus, green tea, especially those enriched with selenium, can improve liver fibrosis through intestinal 5-HT-hepatic 5-HTR signaling.
doi_str_mv 10.1007/s12011-021-02823-x
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Green tea and selenium (Se) can protect the liver from damage; however, the precise mechanism of green tea and the action of Se in green tea on hepatic fibrosis remain unclear. Several studies have demonstrated the profibrogenic role of 5-hydroxytryptamine (5-HT) and 5-hydroxytryptamine receptor (5-HTR) 2A/2B in the liver. The current study aimed to investigate the protective effects and possible mechanisms of selenium-enriched green tea on carbon tetrachloride (CCl 4 )-induced liver fibrosis in male C57BL/6 J mice. After a 4-week intervention with tea solution, histological analysis of the liver showed that green tea interventions alleviated hepatic fibrosis, which was supported by the changes in collagen type I, collagen type III, and α-smooth muscle actin in the liver. Tea interventions significantly inhibited the CCl 4 -provoked increase of duodenal 5-HT and tryptophan hydroxylase and hepatic 5-HT and 5-HTR2A/2B levels. 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subjects Actin
Animals
Biochemistry
Biomedical and Life Sciences
Biotechnology
Carbon
Carbon tetrachloride
Carbon Tetrachloride - toxicity
Collagen
Collagen (type I)
Collagen (type III)
Enrichment
Extracellular
Extracellular matrix
Fibrosis
Green tea
Life Sciences
Liver
Liver - metabolism
Liver Cirrhosis - chemically induced
Liver Cirrhosis - metabolism
Liver Cirrhosis - prevention & control
Male
Mice
Mice, Inbred C57BL
Motivation
Muscles
Nutrition
Oncology
Oxidative stress
Pathogens
Receptors
Selenium
Selenium - metabolism
Serotonin - metabolism
Smooth muscle
Stellate cells
Tea
Tryptophan
Tryptophan hydroxylase
title Protective Effect of Selenium-Enriched Green Tea on Carbon Tetrachloride-Induced Liver Fibrosis
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