Synergistic interaction between praziquantel and oxfendazole or fenbendazole in a murine cysticercosis model.

IF 4.5 2区 医学 Q2 MICROBIOLOGY
Antimicrobial Agents and Chemotherapy Pub Date : 2025-10-01 Epub Date: 2025-08-18 DOI:10.1128/aac.00560-25
Palomares-Alonso Francisca, González-Maciel Angélica, Reynoso-Robles Rafael, Castro Nelly, Pérez-Severiano Francisca, Sánchez-Mendoza Alicia, Jung-Cook Helgi, Bravo Guadalupe, López-Muñoz Francisco
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引用次数: 0

Abstract

Up to date, the pharmacological treatment for active neurocysticercosis (NCC) includes only two drugs, praziquantel and albendazole; however, the clinical response is not always successful, due to its low bioavailability; therefore, new approaches are needed. The aim of the present study was to evaluate the pharmacological interaction between praziquantel (PZQ) and oxfendazole (OXF) in vitro; also, the drug-drug interaction between PZQ and OXF or fenbendazole (FBZ) in vivo using Taenia crassiceps metacestode was assessed. For the in vitro study, the surface of synergistic interaction (SSI) analysis was used to determine the kind of drug interaction between PZQ and OXF. Additionally, morphological and ultrastructural effects were investigated using transmission scanning electron microscopy. For the in vivo study, different doses of PZQ and FBZ or OXF were combined, and the cysticidal effect was determined. In vitro, results showed that 12 combinations exhibited synergism, and four exhibited additive effects. The 1:5 ratio of PZQ and OXF exhibited the highest synergistic effect, with an 11-fold increase in comparison to their theoretical sum. Microscopic observations revealed damage to the tegument and germinal layer; microtriches, flame cells, and muscular fibers were also affected. In vivo, results showed that PZQ + FBZ and PZQ + OXF (ratios 1:4 and 1:1, respectively) exhibited a synergistic reduction of the parasites. The findings of the present study show the potential of these combinations as a pharmacological alternative for cysticercosis treatment. Complementary studies are needed to determine their benefits in the clinical field.

吡喹酮与奥芬达唑或芬苯达唑在小鼠囊虫模型中的协同相互作用。
目前,活动性神经囊虫病(NCC)的药物治疗仅包括吡喹酮和阿苯达唑两种药物;然而,由于其生物利用度低,临床反应并不总是成功的;因此,需要新的方法。本研究的目的是评价吡喹酮(PZQ)和奥芬达唑(OXF)在体外的药理相互作用;同时,采用带绦虫模型,评估PZQ与OXF或芬苯达唑(FBZ)在体内的药物相互作用。体外研究采用协同作用表面(SSI)分析确定PZQ与OXF之间的药物相互作用类型,并通过透射扫描电镜观察其形态和超微结构效应。在体内研究中,将不同剂量的PZQ与FBZ或OXF联合使用,并测定其灭囊效果。体外实验结果显示,12个组合具有协同作用,4个组合具有加性作用。当PZQ与OXF的比例为1:5时,其协同效应最高,达到理论总和的11倍。显微观察发现被皮和生发层有损伤;微鳃、火焰细胞和肌肉纤维也受到影响。体内实验结果表明,PZQ + FBZ和PZQ + OXF(比例分别为1:4和1:1)对寄生虫具有协同抑制作用。本研究的结果表明,这些组合作为治疗囊虫病的药理学替代方案的潜力。需要补充研究来确定它们在临床领域的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.00
自引率
8.20%
发文量
762
审稿时长
3 months
期刊介绍: Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.
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