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New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities
Inflammation is a very common and important pathological process that can cause many diseases. The discovery of anti-inflammatory drugs and the treatment of inflammation are particularly essential. Dammarane-type triterpenoid saponins (PNS) were demonstrated to show anti-inflammatory effects in the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982892/ https://www.ncbi.nlm.nih.gov/pubmed/31905770 http://dx.doi.org/10.3390/molecules25010139 |
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author | Sun, Fan Ruan, Jingya Zhao, Wei Zhang, Ying Xiang, Guilin Yan, Jiejing Hao, Mimi Wu, Lijie Zhang, Yi Wang, Tao |
author_facet | Sun, Fan Ruan, Jingya Zhao, Wei Zhang, Ying Xiang, Guilin Yan, Jiejing Hao, Mimi Wu, Lijie Zhang, Yi Wang, Tao |
author_sort | Sun, Fan |
collection | PubMed |
description | Inflammation is a very common and important pathological process that can cause many diseases. The discovery of anti-inflammatory drugs and the treatment of inflammation are particularly essential. Dammarane-type triterpenoid saponins (PNS) were demonstrated to show anti-inflammatory effects in the leaves of Panax notoginseng. Chromatographies and spectral analysis methods were combined to isolate and identify PNS. Moreover, the nitric oxide (NO) inhibitory activities of all compounds were examined in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. As a result, eleven new dammarane-type triterpenoid saponins, notoginsenosides NL-A(1)–NL-A(4) (1–4), NL-B(1)–NL-B(3) (5–7), NL-C(1)–NL-C(3) (8–10), and NL-D (11) were isolated, and their structures were identified by using various spectrometric techniques and chemical reactions. Among them, compounds 4 and 11 were characterized by the malonyl substitution at 3-position. The 3-malonyl substituted dammarane-type terpennoids were first obtained from natural products. In addition, compounds 1, 2, 5, 6, and 8–10 were found to play an important role in suppressing NO levels at 50 μM, without cytotoxicity. All inhibitory activities were found to be dose-dependent. |
format | Online Article Text |
id | pubmed-6982892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69828922020-02-06 New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities Sun, Fan Ruan, Jingya Zhao, Wei Zhang, Ying Xiang, Guilin Yan, Jiejing Hao, Mimi Wu, Lijie Zhang, Yi Wang, Tao Molecules Article Inflammation is a very common and important pathological process that can cause many diseases. The discovery of anti-inflammatory drugs and the treatment of inflammation are particularly essential. Dammarane-type triterpenoid saponins (PNS) were demonstrated to show anti-inflammatory effects in the leaves of Panax notoginseng. Chromatographies and spectral analysis methods were combined to isolate and identify PNS. Moreover, the nitric oxide (NO) inhibitory activities of all compounds were examined in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. As a result, eleven new dammarane-type triterpenoid saponins, notoginsenosides NL-A(1)–NL-A(4) (1–4), NL-B(1)–NL-B(3) (5–7), NL-C(1)–NL-C(3) (8–10), and NL-D (11) were isolated, and their structures were identified by using various spectrometric techniques and chemical reactions. Among them, compounds 4 and 11 were characterized by the malonyl substitution at 3-position. The 3-malonyl substituted dammarane-type terpennoids were first obtained from natural products. In addition, compounds 1, 2, 5, 6, and 8–10 were found to play an important role in suppressing NO levels at 50 μM, without cytotoxicity. All inhibitory activities were found to be dose-dependent. MDPI 2019-12-29 /pmc/articles/PMC6982892/ /pubmed/31905770 http://dx.doi.org/10.3390/molecules25010139 Text en © 2019 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 Sun, Fan Ruan, Jingya Zhao, Wei Zhang, Ying Xiang, Guilin Yan, Jiejing Hao, Mimi Wu, Lijie Zhang, Yi Wang, Tao New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities |
title | New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities |
title_full | New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities |
title_fullStr | New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities |
title_full_unstemmed | New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities |
title_short | New Dammarane-Type Triterpenoid Saponins from Panax notoginseng Leaves and Their Nitric Oxide Inhibitory Activities |
title_sort | new dammarane-type triterpenoid saponins from panax notoginseng leaves and their nitric oxide inhibitory activities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982892/ https://www.ncbi.nlm.nih.gov/pubmed/31905770 http://dx.doi.org/10.3390/molecules25010139 |
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