Novel anti-Acanthamoebic properties of raloxifene sulfonate/sulfamate derivatives

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular and biochemical parasitology Pub Date : 2023-08-09 DOI:10.1016/j.molbiopara.2023.111582
Ruqaiyyah Siddiqui , Mohammed I. El-Gamal , Sreedevi Sajeev , Seyed-Omar Zaraei , Naveed Ahmed Khan
{"title":"Novel anti-Acanthamoebic properties of raloxifene sulfonate/sulfamate derivatives","authors":"Ruqaiyyah Siddiqui ,&nbsp;Mohammed I. El-Gamal ,&nbsp;Sreedevi Sajeev ,&nbsp;Seyed-Omar Zaraei ,&nbsp;Naveed Ahmed Khan","doi":"10.1016/j.molbiopara.2023.111582","DOIUrl":null,"url":null,"abstract":"<div><p><span><em>Acanthamoeba</em></span><span><span> are known to cause a vision threatening eye infection typically due to contact lens wear, and an infection of the central nervous system. The ability of these amoebae to switch phenotypes, from an active trophozoite to a resistant </span>cyst form is not well understood; the cyst stage is often resistant to chemotherapy, which is of concern given the rise of contact lens use and the ineffective disinfectants available, </span><em>versus</em><span><span><span> the cyst stage. Herein, for the first time, a range of raloxifene sulfonate/sulfamate derivatives which target nucleotide pyrophosphatase/phosphodiesterase </span>enzymes, were assessed using amoebicidal and </span>excystation tests versus the trophozoite and cyst stage of </span><em>Acanthamoeba</em><span>. Moreover, the potential for cytopathogenicity inhibition in amoebae was assessed. Each of the derivatives showed considerable anti-amoebic activity as well as the ability to suppress phenotypic switching (except for compound </span><strong>1a</strong>). Selected raloxifene derivatives reduced <em>Acanthamoeba</em><span>-mediated host cell damage using lactate dehydrogenase assay. These findings suggest that pyrophosphatase/phosphodiesterase enzymes may be valuable targets against </span><em>Acanthamoeba</em> infections.</p></div>","PeriodicalId":18721,"journal":{"name":"Molecular and biochemical parasitology","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2023-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and biochemical parasitology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166685123000403","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Acanthamoeba are known to cause a vision threatening eye infection typically due to contact lens wear, and an infection of the central nervous system. The ability of these amoebae to switch phenotypes, from an active trophozoite to a resistant cyst form is not well understood; the cyst stage is often resistant to chemotherapy, which is of concern given the rise of contact lens use and the ineffective disinfectants available, versus the cyst stage. Herein, for the first time, a range of raloxifene sulfonate/sulfamate derivatives which target nucleotide pyrophosphatase/phosphodiesterase enzymes, were assessed using amoebicidal and excystation tests versus the trophozoite and cyst stage of Acanthamoeba. Moreover, the potential for cytopathogenicity inhibition in amoebae was assessed. Each of the derivatives showed considerable anti-amoebic activity as well as the ability to suppress phenotypic switching (except for compound 1a). Selected raloxifene derivatives reduced Acanthamoeba-mediated host cell damage using lactate dehydrogenase assay. These findings suggest that pyrophosphatase/phosphodiesterase enzymes may be valuable targets against Acanthamoeba infections.

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
雷洛昔芬磺酸酯/氨基磺酸盐衍生物的抗棘阿米巴新特性
众所周知,棘阿米巴会引起威胁视力的眼部感染,通常是由于佩戴隐形眼镜和中枢神经系统感染。这些变形虫将表型从活性滋养体转换为抗性囊肿的能力尚不清楚;与囊肿期相比,囊肿期通常对化疗具有耐药性,考虑到隐形眼镜使用的增加和可用的无效消毒剂,这一点值得关注。在本文中,首次使用杀阿米巴和脱囊试验对一系列靶向核苷酸焦磷酸酶/磷酸二酯酶的雷洛昔芬磺酸酯/氨基磺酸盐衍生物与棘阿米巴的滋养体和囊肿期进行了评估。此外,还评估了变形虫细胞致病性抑制的潜力。每种衍生物都显示出相当大的抗阿米巴活性以及抑制表型转换的能力(化合物1a除外)。使用乳酸脱氢酶测定法,选定的雷洛昔芬衍生物减少了棘阿米巴介导的宿主细胞损伤。这些发现表明,焦磷酸酶/磷酸二酯酶可能是对抗棘阿米巴感染的有价值的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
期刊最新文献
Characterization of two phosphatase 2C domain-containing proteins PPM2A and PPM2B in Toxoplasma gondii. Diversification of sphingolipid synthase activities in kinetoplastid protozoa Biophysical analysis of the membrane-proximal Venus Flytrap domain of ESAG4 receptor-like adenylate cyclase from Trypanosoma brucei Tissue and circulating levels of IL-17A and FoxP3+ in patients with scabies: Correlation with clinical features Using machine learning to dissect host kinases required for Leishmania internalization and development
×
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