Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1

The Arctic-derived fungus Eutypella sp. D-1 can produce numerous secondary metabolites, and some compounds exhibit excellent biological activity. Seven pimarane-type diterpenes, including three new compounds eutypellenone F ( 1 ), libertellenone Y ( 2 ), and libertellenone Z ( 3 ), and four known co...

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Published in:Marine Drugs
Main Authors: Yaodong Ning, Shi Zhang, Te Zheng, Yao Xu, Song Li, Jianpeng Zhang, Binghua Jiao, Yun Zhang, Zengling Ma, Xiaoling Lu
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2023
Subjects:
Online Access:https://doi.org/10.3390/md21100541
https://doaj.org/article/2287c2f0bf9b4dd39ace93caa3e31d4f
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spelling ftdoajarticles:oai:doaj.org/article:2287c2f0bf9b4dd39ace93caa3e31d4f 2023-11-12T04:12:26+01:00 Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1 Yaodong Ning Shi Zhang Te Zheng Yao Xu Song Li Jianpeng Zhang Binghua Jiao Yun Zhang Zengling Ma Xiaoling Lu 2023-10-01T00:00:00Z https://doi.org/10.3390/md21100541 https://doaj.org/article/2287c2f0bf9b4dd39ace93caa3e31d4f EN eng MDPI AG https://www.mdpi.com/1660-3397/21/10/541 https://doaj.org/toc/1660-3397 doi:10.3390/md21100541 1660-3397 https://doaj.org/article/2287c2f0bf9b4dd39ace93caa3e31d4f Marine Drugs, Vol 21, Iss 541, p 541 (2023) Eutypella sp. D-1 diterpene anti-inflammatory zebrafish model Biology (General) QH301-705.5 article 2023 ftdoajarticles https://doi.org/10.3390/md21100541 2023-10-29T00:36:12Z The Arctic-derived fungus Eutypella sp. D-1 can produce numerous secondary metabolites, and some compounds exhibit excellent biological activity. Seven pimarane-type diterpenes, including three new compounds eutypellenone F ( 1 ), libertellenone Y ( 2 ), and libertellenone Z ( 3 ), and four known compounds ( 4 – 7 ), were isolated from fermentation broth of Eutypella sp. D-1 by the OSMAC strategy of adding ethanol as a promoter in the culture medium. Compound 2 has a rare tetrahydrofuran-fused pimarane diterpene skeleton. The anti-inflammatory activity of all compounds was evaluated. Compounds 3 – 6 showed a significant inhibitory effect on cell NO release at 10 μmol/L by in vitro experiments, of which 3 – 5 had inhibitory rates over 60% on nitric oxide (NO) release. Subsequently, the anti-inflammatory activity of 3 – 5 was evaluated based on a zebrafish model, and the results showed that 3 had a significant inhibitory effect on inflammatory cells migration at 40 μmol/L, while 4 and 5 had a significant inhibitory effect at 20 μmol/L. Moreover, compounds 3 – 5 have the same conjugated double bond structure, which may be an important group for these compounds to exert anti-inflammatory activity. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Marine Drugs 21 10 541
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Eutypella sp. D-1
diterpene
anti-inflammatory
zebrafish model
Biology (General)
QH301-705.5
spellingShingle Eutypella sp. D-1
diterpene
anti-inflammatory
zebrafish model
Biology (General)
QH301-705.5
Yaodong Ning
Shi Zhang
Te Zheng
Yao Xu
Song Li
Jianpeng Zhang
Binghua Jiao
Yun Zhang
Zengling Ma
Xiaoling Lu
Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1
topic_facet Eutypella sp. D-1
diterpene
anti-inflammatory
zebrafish model
Biology (General)
QH301-705.5
description The Arctic-derived fungus Eutypella sp. D-1 can produce numerous secondary metabolites, and some compounds exhibit excellent biological activity. Seven pimarane-type diterpenes, including three new compounds eutypellenone F ( 1 ), libertellenone Y ( 2 ), and libertellenone Z ( 3 ), and four known compounds ( 4 – 7 ), were isolated from fermentation broth of Eutypella sp. D-1 by the OSMAC strategy of adding ethanol as a promoter in the culture medium. Compound 2 has a rare tetrahydrofuran-fused pimarane diterpene skeleton. The anti-inflammatory activity of all compounds was evaluated. Compounds 3 – 6 showed a significant inhibitory effect on cell NO release at 10 μmol/L by in vitro experiments, of which 3 – 5 had inhibitory rates over 60% on nitric oxide (NO) release. Subsequently, the anti-inflammatory activity of 3 – 5 was evaluated based on a zebrafish model, and the results showed that 3 had a significant inhibitory effect on inflammatory cells migration at 40 μmol/L, while 4 and 5 had a significant inhibitory effect at 20 μmol/L. Moreover, compounds 3 – 5 have the same conjugated double bond structure, which may be an important group for these compounds to exert anti-inflammatory activity.
format Article in Journal/Newspaper
author Yaodong Ning
Shi Zhang
Te Zheng
Yao Xu
Song Li
Jianpeng Zhang
Binghua Jiao
Yun Zhang
Zengling Ma
Xiaoling Lu
author_facet Yaodong Ning
Shi Zhang
Te Zheng
Yao Xu
Song Li
Jianpeng Zhang
Binghua Jiao
Yun Zhang
Zengling Ma
Xiaoling Lu
author_sort Yaodong Ning
title Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1
title_short Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1
title_full Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1
title_fullStr Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1
title_full_unstemmed Pimarane-Type Diterpenes with Anti-Inflammatory Activity from Arctic-Derived Fungus Eutypella sp. D-1
title_sort pimarane-type diterpenes with anti-inflammatory activity from arctic-derived fungus eutypella sp. d-1
publisher MDPI AG
publishDate 2023
url https://doi.org/10.3390/md21100541
https://doaj.org/article/2287c2f0bf9b4dd39ace93caa3e31d4f
genre Arctic
genre_facet Arctic
op_source Marine Drugs, Vol 21, Iss 541, p 541 (2023)
op_relation https://www.mdpi.com/1660-3397/21/10/541
https://doaj.org/toc/1660-3397
doi:10.3390/md21100541
1660-3397
https://doaj.org/article/2287c2f0bf9b4dd39ace93caa3e31d4f
op_doi https://doi.org/10.3390/md21100541
container_title Marine Drugs
container_volume 21
container_issue 10
container_start_page 541
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