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海洋生物作为预防和治疗疟疾的天然产物潜在来源。

Marine organisms as potential sources of natural products for the prevention and treatment of malaria.

作者信息

Negm Walaa A, Ezzat Shahira M, Zayed Ahmed

机构信息

Department of Pharmacognosy, Tanta University, College of Pharmacy El-Guish Street Tanta 31527 Egypt

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University Kasr El-Aini Street Cairo 11562 Egypt

出版信息

RSC Adv. 2023 Feb 2;13(7):4436-4475. doi: 10.1039/d2ra07977a. eCollection 2023 Jan 31.

Abstract

Vector-borne diseases (VBDs) are a worldwide critical concern accounting for 17% of the estimated global burden of all infectious diseases in 2020. Despite the various medicines available for the management, the deadliest VBD malaria, caused by sp., has resulted in hundreds of thousands of deaths in sub-Saharan Africa only. This finding may be explained by the progressive loss of antimalarial medication efficacy, inherent toxicity, the rise of drug resistance, or a lack of treatment adherence. As a result, new drug discoveries from uncommon sources are desperately needed, especially against multi-drug resistant strains. Marine organisms have been investigated, including sponges, soft corals, algae, and cyanobacteria. They have been shown to produce many bioactive compounds that potentially affect the causative organism at different stages of its life cycle, including the chloroquine (CQ)-resistant strains of . These compounds also showed diverse chemical structures belonging to various phytochemical classes, including alkaloids, terpenoids, polyketides, macrolides, and others. The current article presents a comprehensive review of marine-derived natural products with antimalarial activity as potential candidates for targeting different stages and species of in both and and in comparison with the commercially available and terrestrial plant-derived products, , quinine and artemisinin.

摘要

媒介传播疾病(VBDs)是一个全球性的重大问题,在2020年估计占全球所有传染病负担的17%。尽管有各种药物可用于治疗,但由疟原虫引起的最致命的VBD疟疾仅在撒哈拉以南非洲就导致了数十万人死亡。这一发现可能是由于抗疟药物疗效的逐渐丧失、固有的毒性、耐药性的上升或治疗依从性的缺乏。因此,迫切需要从不常见来源发现新的药物,尤其是针对多重耐药菌株的药物。人们已经对海洋生物进行了研究,包括海绵、软珊瑚、藻类和蓝细菌。研究表明,它们能产生许多生物活性化合物,这些化合物可能在疟原虫生命周期的不同阶段影响病原体,包括对氯喹(CQ)耐药的疟原虫菌株。这些化合物还显示出属于各种植物化学类别的多样化学结构,包括生物碱、萜类化合物、聚酮化合物、大环内酯类化合物等。本文全面综述了具有抗疟活性的海洋天然产物,这些天然产物作为潜在候选物,可针对疟原虫的不同阶段和种类,无论是在体外还是体内,并且与市售的和陆地植物来源的产品(如氯喹、奎宁和青蒿素)进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1572/9892989/fe67ef37f8bf/d2ra07977a-f1.jpg

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