{"title":"蘑菇Cyathus striatus CBPFE A06培养次生代谢物的分子特性、结构、神经营养和抗炎活性","authors":"Jing Wei, Mei-Yu Ye, Zhen-Xin Wang, Yi-Lin Zhang, Xuan-Sheng Hu, He-Ping Hui, Yi-Tong Liu, Jianzhao Qi","doi":"10.1080/14786419.2023.2273911","DOIUrl":null,"url":null,"abstract":"<p><p>Two previously undescribed natural cyathane diterpenoids Me-dentifragilin A (<b>1</b>) and Epi-neocyathin O (<b>2</b>), and three known cyathane diterpenoids <b>3</b>-<b>5</b>, cyathin O, neocyathin P, and cyathin I, were isolated from the rice medium of the <i>Cyathus striatus</i> CBPFE A06. Their structures were established by NMR spectra, and HR-ESI-MS. Compounds <b>1</b>-<b>5</b> displayed encouraging neurotrophic activity in PC-12 cells at doses of 5 µM. Meanwhile, <b>1</b>-<b>5</b> significantly inhibited LPS-induced NO generation in BV2 cells with the IC<sub>50</sub> values ranging from 2.44 ± 0.16 to 4.33 ± 0.32 μM. Western blot analysis showed that <b>2</b> and <b>4</b> inhibited the expression of genes involved in nitric oxide (NO) production. Molecular docking revealed that five residues of inducible NO synthase (iNOS) are key residues affecting the interaction of <b>2</b> and <b>4</b> with iNOS. This study enriches the structural diversity of cyathane diterpenes and adds to the evidence that cyathane diterpenes prevent and treat neurodegenerative diseases.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"4280-4285"},"PeriodicalIF":1.9000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular properties, structure, neurotrophic and anti-inflammatory activities of cultured secondary metabolites from the cultures of the mushroom <i>Cyathus striatus</i> CBPFE A06.\",\"authors\":\"Jing Wei, Mei-Yu Ye, Zhen-Xin Wang, Yi-Lin Zhang, Xuan-Sheng Hu, He-Ping Hui, Yi-Tong Liu, Jianzhao Qi\",\"doi\":\"10.1080/14786419.2023.2273911\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Two previously undescribed natural cyathane diterpenoids Me-dentifragilin A (<b>1</b>) and Epi-neocyathin O (<b>2</b>), and three known cyathane diterpenoids <b>3</b>-<b>5</b>, cyathin O, neocyathin P, and cyathin I, were isolated from the rice medium of the <i>Cyathus striatus</i> CBPFE A06. Their structures were established by NMR spectra, and HR-ESI-MS. Compounds <b>1</b>-<b>5</b> displayed encouraging neurotrophic activity in PC-12 cells at doses of 5 µM. Meanwhile, <b>1</b>-<b>5</b> significantly inhibited LPS-induced NO generation in BV2 cells with the IC<sub>50</sub> values ranging from 2.44 ± 0.16 to 4.33 ± 0.32 μM. Western blot analysis showed that <b>2</b> and <b>4</b> inhibited the expression of genes involved in nitric oxide (NO) production. Molecular docking revealed that five residues of inducible NO synthase (iNOS) are key residues affecting the interaction of <b>2</b> and <b>4</b> with iNOS. This study enriches the structural diversity of cyathane diterpenes and adds to the evidence that cyathane diterpenes prevent and treat neurodegenerative diseases.</p>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\" \",\"pages\":\"4280-4285\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1080/14786419.2023.2273911\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/10/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2023.2273911","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/25 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Molecular properties, structure, neurotrophic and anti-inflammatory activities of cultured secondary metabolites from the cultures of the mushroom Cyathus striatus CBPFE A06.
Two previously undescribed natural cyathane diterpenoids Me-dentifragilin A (1) and Epi-neocyathin O (2), and three known cyathane diterpenoids 3-5, cyathin O, neocyathin P, and cyathin I, were isolated from the rice medium of the Cyathus striatus CBPFE A06. Their structures were established by NMR spectra, and HR-ESI-MS. Compounds 1-5 displayed encouraging neurotrophic activity in PC-12 cells at doses of 5 µM. Meanwhile, 1-5 significantly inhibited LPS-induced NO generation in BV2 cells with the IC50 values ranging from 2.44 ± 0.16 to 4.33 ± 0.32 μM. Western blot analysis showed that 2 and 4 inhibited the expression of genes involved in nitric oxide (NO) production. Molecular docking revealed that five residues of inducible NO synthase (iNOS) are key residues affecting the interaction of 2 and 4 with iNOS. This study enriches the structural diversity of cyathane diterpenes and adds to the evidence that cyathane diterpenes prevent and treat neurodegenerative diseases.
期刊介绍:
The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds.
The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal.
Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section.
All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.