7-hydroxy-4′- methoxy isoflavone 对大肠利什曼原虫的抗寄生和细胞毒性作用

Q3 Pharmacology, Toxicology and Pharmaceutics Journal of HerbMed Pharmacology Pub Date : 2023-08-10 DOI:10.34172/jhp.2023.44897
Mahdi Aghaei, Farhood Alizadegan, Yosra Raziani, Githa Kishore, Massumeh Saadatmand, Suja Ajoy Kumar
{"title":"7-hydroxy-4′- methoxy isoflavone 对大肠利什曼原虫的抗寄生和细胞毒性作用","authors":"Mahdi Aghaei, Farhood Alizadegan, Yosra Raziani, Githa Kishore, Massumeh Saadatmand, Suja Ajoy Kumar","doi":"10.34172/jhp.2023.44897","DOIUrl":null,"url":null,"abstract":"Introduction: Leishmaniasis caused by Leishmania spp. is observed in most parts of the world. Although, glucantime, a pentavalent antimony compound, and other synthetic drugs are broadly applied for leishmaniasis therapy; however, the use of these synthetic agents has some limitations. Hence, this study was designed to assess the inhibiting effects of 7-hydroxy4′-methoxyisoflavone (7HMI) against promastigote and amastigote stages of Leishmania major in vitro. Methods: The MTT assay was applied to study the antileishmanial activity of 7HMI against promastigotes and its cytotoxicity effects on macrophage cells. The nitric oxide (NO) produced by the treated macrophage cells with 7HMI was also assessed. Results: 7HMI considerably (P<0.05) inhibited the growth rate of promastigotes and amastigotes stages. The 50% inhibitory concentrations of 7HMI and glucantim were 11.3 and 15.4 µg/mL for promastigote and amastigote, respectively. 7HMI, especially at 1/3 IC50 and 1/2 IC50 concentrations, considerably triggered the NO release. Conclusion: The current research findings reported the favorable antileishmanial effects of 7HMI against L. major with possible mechanisms such as reducing the infectivity rate of macrophage cells and provoking NO creation. Nevertheless, more research must be performed to clear its efficacy in animal model and then in human.","PeriodicalId":15934,"journal":{"name":"Journal of HerbMed Pharmacology","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antiparasitic and cytotoxicity effects of 7-hydroxy-4′- methoxy isoflavone against Leishmania major\",\"authors\":\"Mahdi Aghaei, Farhood Alizadegan, Yosra Raziani, Githa Kishore, Massumeh Saadatmand, Suja Ajoy Kumar\",\"doi\":\"10.34172/jhp.2023.44897\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Leishmaniasis caused by Leishmania spp. is observed in most parts of the world. Although, glucantime, a pentavalent antimony compound, and other synthetic drugs are broadly applied for leishmaniasis therapy; however, the use of these synthetic agents has some limitations. Hence, this study was designed to assess the inhibiting effects of 7-hydroxy4′-methoxyisoflavone (7HMI) against promastigote and amastigote stages of Leishmania major in vitro. Methods: The MTT assay was applied to study the antileishmanial activity of 7HMI against promastigotes and its cytotoxicity effects on macrophage cells. The nitric oxide (NO) produced by the treated macrophage cells with 7HMI was also assessed. Results: 7HMI considerably (P<0.05) inhibited the growth rate of promastigotes and amastigotes stages. The 50% inhibitory concentrations of 7HMI and glucantim were 11.3 and 15.4 µg/mL for promastigote and amastigote, respectively. 7HMI, especially at 1/3 IC50 and 1/2 IC50 concentrations, considerably triggered the NO release. Conclusion: The current research findings reported the favorable antileishmanial effects of 7HMI against L. major with possible mechanisms such as reducing the infectivity rate of macrophage cells and provoking NO creation. Nevertheless, more research must be performed to clear its efficacy in animal model and then in human.\",\"PeriodicalId\":15934,\"journal\":{\"name\":\"Journal of HerbMed Pharmacology\",\"volume\":\"38 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of HerbMed Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.34172/jhp.2023.44897\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of HerbMed Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34172/jhp.2023.44897","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

摘要

导言:由利什曼原虫引起的利什曼病在世界大部分地区都有发生。虽然五价锑化合物葡糖酸和其他合成药物被广泛用于利什曼病的治疗,但这些合成药物的使用有一定的局限性。因此,本研究旨在评估 7-羟基 4′-甲氧基异黄酮(7HMI)对体外大利什曼原虫和非原虫阶段的抑制作用。方法:采用 MTT 法研究 7HMI 对原体的抗利什曼活性及其对巨噬细胞的细胞毒性作用。此外,还评估了经 7HMI 处理的巨噬细胞产生的一氧化氮(NO)。结果显示7HMI能显著(P<0.05)抑制原虫和非原虫阶段的生长速度。7HMI 和葡甘定对原虫和非原虫的 50% 抑制浓度分别为 11.3 和 15.4 µg/mL。7HMI,尤其是在1/3 IC50和1/2 IC50浓度下,可显著促进NO的释放。结论目前的研究结果表明,7HMI 对大肠杆菌具有良好的抗利什曼病作用,其可能的机制包括降低巨噬细胞的感染率和促进 NO 的产生。尽管如此,还必须开展更多的研究,以明确其在动物模型和人体中的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Antiparasitic and cytotoxicity effects of 7-hydroxy-4′- methoxy isoflavone against Leishmania major
Introduction: Leishmaniasis caused by Leishmania spp. is observed in most parts of the world. Although, glucantime, a pentavalent antimony compound, and other synthetic drugs are broadly applied for leishmaniasis therapy; however, the use of these synthetic agents has some limitations. Hence, this study was designed to assess the inhibiting effects of 7-hydroxy4′-methoxyisoflavone (7HMI) against promastigote and amastigote stages of Leishmania major in vitro. Methods: The MTT assay was applied to study the antileishmanial activity of 7HMI against promastigotes and its cytotoxicity effects on macrophage cells. The nitric oxide (NO) produced by the treated macrophage cells with 7HMI was also assessed. Results: 7HMI considerably (P<0.05) inhibited the growth rate of promastigotes and amastigotes stages. The 50% inhibitory concentrations of 7HMI and glucantim were 11.3 and 15.4 µg/mL for promastigote and amastigote, respectively. 7HMI, especially at 1/3 IC50 and 1/2 IC50 concentrations, considerably triggered the NO release. Conclusion: The current research findings reported the favorable antileishmanial effects of 7HMI against L. major with possible mechanisms such as reducing the infectivity rate of macrophage cells and provoking NO creation. Nevertheless, more research must be performed to clear its efficacy in animal model and then in human.
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
Journal of HerbMed Pharmacology
Journal of HerbMed Pharmacology Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
2.50
自引率
0.00%
发文量
49
审稿时长
12 weeks
期刊介绍: Journal of Herbmed Pharmacology (J Herbmed Pharmacol) is the intersection between medicinal plants and pharmacology. This international journal publishes manuscripts in the fields of medicinal plants, pharmacology and therapeutic. This journal aims to reach all relevant national and international medical institutions and persons in electronic version free of charge. J Herbmed Pharmacol has pursued this aim through publishing editorials, original research articles, reviews, mini-reviews, commentaries, letters to the editor, hypothesis, case reports, epidemiology and prevention, news and views. In this journal, particular emphasis is given to research, both experimental and clinical, aimed at protection/prevention of diseases. A further aim of this journal is to emphasize and strengthen the link between herbalists and pharmacologists. In addition, J Herbmed Pharmacol welcomes basic biomedical as well as pharmaceutical scientific research applied to clinical pharmacology. Contributions in any of these formats are invited for editorial consideration following peer review by at least two experts in the field.
期刊最新文献
Epigallocatechin gallate, the primary bioactive component from Camellia sinensis: A review on immunomodulatory effects in autoimmune diseases by balancing the differentiation of Th and Treg cells Rethinking the basic action modes of herbal medicine and pondering classical standardization Exploring the anti-acne potential of Muntingia calabura L leaves against Staphylococcus epidermidis: In vitro and in silico perspective Solanum trilobatum leaf extract-derived silver nanoparticles downregulate the PI3K/AKT/mTOR signaling pathway and attenuate oral squamous cell carcinoma cell proliferation Integrative computational approaches for designing novel alpha-glucosidase inhibitors based on curculigoside A derivatives: Virtual screening, molecular docking, and molecular dynamics
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1