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SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects

Patients with liver cirrhosis also have subtle cardiac structure or function abnormalities. This cardiac dysfunction commonly occurs in 56% of waiting orthotopic liver transplantation (OLT) patients and is defined as cirrhotic cardiomyopathy (CCM). Up to now, there is no standard treatment because C...

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Autores principales: Yang, Cheng-Hsun, Ting, Wei-Jen, Day, Cecilia Hsuan, Ju, Da-Tong, Yeh, Yu-Lan, Chung, Li-Chin, Tsai, Fu-Jenn, Tsai, Chang-Hai, Tsai, Yuhsin, Huang, Chih-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057717/
https://www.ncbi.nlm.nih.gov/pubmed/24815066
http://dx.doi.org/10.3390/ijms15058037
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author Yang, Cheng-Hsun
Ting, Wei-Jen
Day, Cecilia Hsuan
Ju, Da-Tong
Yeh, Yu-Lan
Chung, Li-Chin
Tsai, Fu-Jenn
Tsai, Chang-Hai
Tsai, Yuhsin
Huang, Chih-Yang
author_facet Yang, Cheng-Hsun
Ting, Wei-Jen
Day, Cecilia Hsuan
Ju, Da-Tong
Yeh, Yu-Lan
Chung, Li-Chin
Tsai, Fu-Jenn
Tsai, Chang-Hai
Tsai, Yuhsin
Huang, Chih-Yang
author_sort Yang, Cheng-Hsun
collection PubMed
description Patients with liver cirrhosis also have subtle cardiac structure or function abnormalities. This cardiac dysfunction commonly occurs in 56% of waiting orthotopic liver transplantation (OLT) patients and is defined as cirrhotic cardiomyopathy (CCM). Up to now, there is no standard treatment because CCM does not have a solidly established diagnosis and is based on high clinical suspicion. The liver function of CCM is particularly limited, making patients vulnerable to more drug treatments. Here, we use silymarin (100 mg/kg/day), baicalein (30 mg/kg/day), San Huang Shel Shin Tang (SHSST, 30 mg/kg/day) and β-cyclodextrin modified SHSST (SHSSTc, 30 and 300 mg/kg/day) treatments for a CCl(4)-induced CCM rat model. The results show that silymarin, baicalein and SHSST treatments can only slightly reduce the collagen accumulation in CCM rat hearts. However, SHSSTc treatment protects the heart in CCM and significantly inhibits collagen acumination and the fibrosis regulating transforming growth factor-β (TGF-β) pathway expression. SHSSTc treatments further reduced the heart weight and the ratio between left ventricular weight (LVW) and tibia length (TL). This experimental data show that water solubility improved β-cyclodextrin modified Chinese herbal medicine formula (SHSSTc) can provide an excellent heart protection effect through TGF-β pathway inhibition.
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spelling pubmed-40577172014-06-16 SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects Yang, Cheng-Hsun Ting, Wei-Jen Day, Cecilia Hsuan Ju, Da-Tong Yeh, Yu-Lan Chung, Li-Chin Tsai, Fu-Jenn Tsai, Chang-Hai Tsai, Yuhsin Huang, Chih-Yang Int J Mol Sci Article Patients with liver cirrhosis also have subtle cardiac structure or function abnormalities. This cardiac dysfunction commonly occurs in 56% of waiting orthotopic liver transplantation (OLT) patients and is defined as cirrhotic cardiomyopathy (CCM). Up to now, there is no standard treatment because CCM does not have a solidly established diagnosis and is based on high clinical suspicion. The liver function of CCM is particularly limited, making patients vulnerable to more drug treatments. Here, we use silymarin (100 mg/kg/day), baicalein (30 mg/kg/day), San Huang Shel Shin Tang (SHSST, 30 mg/kg/day) and β-cyclodextrin modified SHSST (SHSSTc, 30 and 300 mg/kg/day) treatments for a CCl(4)-induced CCM rat model. The results show that silymarin, baicalein and SHSST treatments can only slightly reduce the collagen accumulation in CCM rat hearts. However, SHSSTc treatment protects the heart in CCM and significantly inhibits collagen acumination and the fibrosis regulating transforming growth factor-β (TGF-β) pathway expression. SHSSTc treatments further reduced the heart weight and the ratio between left ventricular weight (LVW) and tibia length (TL). This experimental data show that water solubility improved β-cyclodextrin modified Chinese herbal medicine formula (SHSSTc) can provide an excellent heart protection effect through TGF-β pathway inhibition. Molecular Diversity Preservation International (MDPI) 2014-05-08 /pmc/articles/PMC4057717/ /pubmed/24815066 http://dx.doi.org/10.3390/ijms15058037 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Yang, Cheng-Hsun
Ting, Wei-Jen
Day, Cecilia Hsuan
Ju, Da-Tong
Yeh, Yu-Lan
Chung, Li-Chin
Tsai, Fu-Jenn
Tsai, Chang-Hai
Tsai, Yuhsin
Huang, Chih-Yang
SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects
title SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects
title_full SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects
title_fullStr SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects
title_full_unstemmed SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects
title_short SHSST Cyclodextrin Complex Prevents the Fibrosis Effect on CCl(4)-Induced Cirrhotic Cardiomyopathy in Rats through TGF-β Pathway Inhibition Effects
title_sort shsst cyclodextrin complex prevents the fibrosis effect on ccl(4)-induced cirrhotic cardiomyopathy in rats through tgf-β pathway inhibition effects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057717/
https://www.ncbi.nlm.nih.gov/pubmed/24815066
http://dx.doi.org/10.3390/ijms15058037
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