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Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus

In the dimethylnitrosamine (DMN)-induced hepatic fibrosis Wistar rat model, the mycelium extract of Phellinus linteus (PLE) (20 mg/Kg) displayed significant protection against hepatic fibrosis. The present investigation characterized eleven new ionone derivatives, phellinulins D–N (4–14), from the P...

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Autores principales: Huang, Shiow-Chyn, Wang, Pei-Wen, Kuo, Ping-Chung, Hung, Hsin-Yi, Pan, Tai-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099599/
https://www.ncbi.nlm.nih.gov/pubmed/30002357
http://dx.doi.org/10.3390/molecules23071705
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author Huang, Shiow-Chyn
Wang, Pei-Wen
Kuo, Ping-Chung
Hung, Hsin-Yi
Pan, Tai-Long
author_facet Huang, Shiow-Chyn
Wang, Pei-Wen
Kuo, Ping-Chung
Hung, Hsin-Yi
Pan, Tai-Long
author_sort Huang, Shiow-Chyn
collection PubMed
description In the dimethylnitrosamine (DMN)-induced hepatic fibrosis Wistar rat model, the mycelium extract of Phellinus linteus (PLE) (20 mg/Kg) displayed significant protection against hepatic fibrosis. The present investigation characterized eleven new ionone derivatives, phellinulins D–N (4–14), from the P. linteus mycelium extract and the relative stereochemical structures were constructed according to the spectroscopic and spectrometric analytical results. Some purified compounds were examined for their inhibitory effects on activated rat hepatic stellate cells (HSCs) and several isolates did exhibit significant protection. The results indicated that the mycelium of P. linteus could be explored as a hepatoprotective drug or healthy food candidate in the near future.
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spelling pubmed-60995992018-11-13 Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus Huang, Shiow-Chyn Wang, Pei-Wen Kuo, Ping-Chung Hung, Hsin-Yi Pan, Tai-Long Molecules Article In the dimethylnitrosamine (DMN)-induced hepatic fibrosis Wistar rat model, the mycelium extract of Phellinus linteus (PLE) (20 mg/Kg) displayed significant protection against hepatic fibrosis. The present investigation characterized eleven new ionone derivatives, phellinulins D–N (4–14), from the P. linteus mycelium extract and the relative stereochemical structures were constructed according to the spectroscopic and spectrometric analytical results. Some purified compounds were examined for their inhibitory effects on activated rat hepatic stellate cells (HSCs) and several isolates did exhibit significant protection. The results indicated that the mycelium of P. linteus could be explored as a hepatoprotective drug or healthy food candidate in the near future. MDPI 2018-07-12 /pmc/articles/PMC6099599/ /pubmed/30002357 http://dx.doi.org/10.3390/molecules23071705 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huang, Shiow-Chyn
Wang, Pei-Wen
Kuo, Ping-Chung
Hung, Hsin-Yi
Pan, Tai-Long
Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus
title Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus
title_full Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus
title_fullStr Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus
title_full_unstemmed Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus
title_short Hepatoprotective Principles and Other Chemical Constituents from the Mycelium of Phellinus linteus
title_sort hepatoprotective principles and other chemical constituents from the mycelium of phellinus linteus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099599/
https://www.ncbi.nlm.nih.gov/pubmed/30002357
http://dx.doi.org/10.3390/molecules23071705
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