巴豆急性口服毒性、抗肿瘤、抗菌和抗氧化活性的GC-MS分析与评价。航空部件:体外、体内和计算机研究。

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Ibrahim Ali Al-Hakami , Amina El-Shaibany , Hassan Al-Mahbashi , Ahmed S. Abdelkhalek , Mahmoud M. Elaasser , Ali E. Raslan
{"title":"巴豆急性口服毒性、抗肿瘤、抗菌和抗氧化活性的GC-MS分析与评价。航空部件:体外、体内和计算机研究。","authors":"Ibrahim Ali Al-Hakami ,&nbsp;Amina El-Shaibany ,&nbsp;Hassan Al-Mahbashi ,&nbsp;Ahmed S. Abdelkhalek ,&nbsp;Mahmoud M. Elaasser ,&nbsp;Ali E. Raslan","doi":"10.1080/14786419.2023.2280820","DOIUrl":null,"url":null,"abstract":"<div><div><em>Croton socotranus</em> Balf.f. shrub is widely used traditionally in Asia as an anti-infective. The study was conducted for metabolite profiling, oral acute toxicity and antioxidant studies, antimicrobial activity and anticancer effect against human hepatoma (HepG2), breast cancer (MCF-7) and rhabdomyosarcoma (RD) cells. Gas chromatography-mass spectrometry analysis revealed the presence of 39 compounds, predominantly comprising fatty acids (57.76%), sesquiterpenes (24.56%) and triterpenes (9.54%). The <em>n</em>-hexane fraction exhibited promising antimicrobial activity and displayed a potent anti-tumour effect against HepG2, MCF-7 and RD cells with IC<sub>50</sub> values of 3.4, 6.5 and 7.1 μg/mL, respectively. Histological examination revealed significant morphological changes consistent with the changes observed in the apoptotic mechanism of action. The molecular docking study provided insights into the rational binding modes of the identified compounds with phosphoinositide 3-kinase and poly(ADP-ribose)polymerase-1 enzymes. Our findings suggest the potential of <em>C. socotranus</em> as a valuable source of antimicrobial and anticancer agents.</div></div>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":"38 24","pages":"Pages 4307-4316"},"PeriodicalIF":1.9000,"publicationDate":"2023-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"GC-MS profiling and evaluation of acute oral toxicity, anti-tumour, antimicrobial and antioxidant activities of Croton socotranus Balf.f. aerial parts: in-vitro, in-vivo and in-silico studies\",\"authors\":\"Ibrahim Ali Al-Hakami ,&nbsp;Amina El-Shaibany ,&nbsp;Hassan Al-Mahbashi ,&nbsp;Ahmed S. Abdelkhalek ,&nbsp;Mahmoud M. Elaasser ,&nbsp;Ali E. Raslan\",\"doi\":\"10.1080/14786419.2023.2280820\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Croton socotranus</em> Balf.f. shrub is widely used traditionally in Asia as an anti-infective. The study was conducted for metabolite profiling, oral acute toxicity and antioxidant studies, antimicrobial activity and anticancer effect against human hepatoma (HepG2), breast cancer (MCF-7) and rhabdomyosarcoma (RD) cells. Gas chromatography-mass spectrometry analysis revealed the presence of 39 compounds, predominantly comprising fatty acids (57.76%), sesquiterpenes (24.56%) and triterpenes (9.54%). The <em>n</em>-hexane fraction exhibited promising antimicrobial activity and displayed a potent anti-tumour effect against HepG2, MCF-7 and RD cells with IC<sub>50</sub> values of 3.4, 6.5 and 7.1 μg/mL, respectively. Histological examination revealed significant morphological changes consistent with the changes observed in the apoptotic mechanism of action. The molecular docking study provided insights into the rational binding modes of the identified compounds with phosphoinositide 3-kinase and poly(ADP-ribose)polymerase-1 enzymes. Our findings suggest the potential of <em>C. socotranus</em> as a valuable source of antimicrobial and anticancer agents.</div></div>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\"38 24\",\"pages\":\"Pages 4307-4316\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2023-11-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1478641923022726\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1478641923022726","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

摘要

牛膝草;灌木在亚洲传统上被广泛用作抗感染药。该研究旨在进行代谢物分析、口服急性毒性和抗氧化研究、抗菌活性和对人肝癌(HepG2)、乳腺癌(MCF-7)和横纹肌肉瘤(RD)细胞的抗癌作用。经气相色谱-质谱分析,共鉴定出39种化合物,主要包括脂肪酸(57.76%)、倍半萜(24.56%)和三萜(9.54%)。正己烷部分对HepG2、MCF-7和RD细胞具有较强的抗肿瘤作用,IC50值分别为3.4、6.5和7.1 μg/mL。组织学检查显示明显的形态学改变与凋亡作用机制的变化一致。分子对接研究揭示了所鉴定化合物与磷酸肌肽3-激酶和聚(adp -核糖)聚合酶-1酶的合理结合模式。我们的研究结果表明,socotranus可能是一种有价值的抗菌和抗癌药物来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GC-MS profiling and evaluation of acute oral toxicity, anti-tumour, antimicrobial and antioxidant activities of Croton socotranus Balf.f. aerial parts: in-vitro, in-vivo and in-silico studies
Croton socotranus Balf.f. shrub is widely used traditionally in Asia as an anti-infective. The study was conducted for metabolite profiling, oral acute toxicity and antioxidant studies, antimicrobial activity and anticancer effect against human hepatoma (HepG2), breast cancer (MCF-7) and rhabdomyosarcoma (RD) cells. Gas chromatography-mass spectrometry analysis revealed the presence of 39 compounds, predominantly comprising fatty acids (57.76%), sesquiterpenes (24.56%) and triterpenes (9.54%). The n-hexane fraction exhibited promising antimicrobial activity and displayed a potent anti-tumour effect against HepG2, MCF-7 and RD cells with IC50 values of 3.4, 6.5 and 7.1 μg/mL, respectively. Histological examination revealed significant morphological changes consistent with the changes observed in the apoptotic mechanism of action. The molecular docking study provided insights into the rational binding modes of the identified compounds with phosphoinositide 3-kinase and poly(ADP-ribose)polymerase-1 enzymes. Our findings suggest the potential of C. socotranus as a valuable source of antimicrobial and anticancer agents.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信