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三磷酸对甲苯磺酸盐,一种单一的、口服的杀血吸虫前药:体内疗效、处置和代谢特征。

TPT sulfonate, a single, oral dose schistosomicidal prodrug: In vivo efficacy, disposition and metabolic profiling.

机构信息

Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, 533 Parnassus Ave, San Francisco, CA, 94143, USA; Center for Discovery and Innovation in Parasitic Diseases, University of California, 1700 4th St, San Francisco, CA, 94158, USA.

Center for Discovery and Innovation in Parasitic Diseases, University of California, 1700 4th St, San Francisco, CA, 94158, USA; Department of Pharmaceutical Chemistry, University of California, 1700 4th St, San Francisco, CA, 94158, USA.

出版信息

Int J Parasitol Drugs Drug Resist. 2018 Dec;8(3):571-586. doi: 10.1016/j.ijpddr.2018.10.004. Epub 2018 Nov 20.

Abstract

Treatment of schistosomiasis relies precariously on just one drug, praziquantel (PZQ). In the search for alternatives, 15 S-[2-(alkylamino)alkane] thiosulfuric acids were obtained from a previous research program and profiled in mice for efficacy against both mature (>42-day-old) and juvenile (21-day-old) Schistosoma mansoni using a screening dose of 100 mg/kg PO QDx4. One compound, S-[2-(tert-butylamino)-1-phenylethane] thiosulfuric acid (TPT sulfonate), was the most effective by decreasing female and male worm burdens by ≥ 90% and ≥46% (mature), and ≥89% and ≥79% (juvenile), respectively. In contrast, PZQ decreased mature female and male worm burdens by 95% and 94%, respectively, but was ineffective against juvenile stages. Against 7-day-old lung-stage worms, TPT sulfonate was only effective at twice the dose decreasing female and male burdens by 95 and 80%, respectively. Single oral doses at 400 and/or 600 mg/kg across various developmental time-points (1-, 7-, 15-, 21- and/or 42 day-old) were consistent with the QD x4 data; efficacy was strongest once the parasites had completed lung migration, and female and male burdens were decreased by at least 90% and 80%, respectively. In vitro, TPT sulfonate is inactive against the parasite suggesting a pro-drug mechanism of action. In mice, TPT sulfonate is fully absorbed and subject to rapid, non-CYP-mediated, first-pass metabolism that is initiated by desulfation and yields a series of metabolites. The initially-formed free thiol-containing metabolite, termed TP thiol, was chemically synthesized; it dose-dependently decreased S. mansoni and Schistosoma haematobium motility in vitro. Also, when administered as a single 50 mg/kg IP dose, TP thiol decreased 33-day-old S. mansoni female and male burdens by 35% and 44%, with less severe organomegaly. Overall, TPT sulfonate's efficacy profile is competitive with that of PZQ. Also, the characterization of a parasiticidal metabolite facilitates an understanding and improvement of the chemistry, and identification of the mechanism of action and/or target.

摘要

治疗血吸虫病严重依赖于一种药物,即吡喹酮(PZQ)。在寻找替代品的过程中,从以前的研究项目中获得了 15 种[S-[2-(烷基氨基)烷]硫代硫酸酯,并在小鼠中进行了功效分析,使用 100mg/kg PO QDx4 的筛选剂量,针对成熟(>42 天龄)和幼体(21 天龄)曼氏血吸虫进行了分析。一种化合物,S-[2-(叔丁基氨基)-1-苯乙烷]硫代硫酸酯(TPT 硫酸盐),通过降低雌性和雄性虫体负担≥90%和≥46%(成熟)和≥89%和≥79%(幼体),是最有效的。相比之下,PZQ 降低成熟雌性和雄性虫体负担的幅度分别为 95%和 94%,但对幼体阶段无效。对于 7 日龄的肺期蠕虫,TPT 硫酸盐仅在两倍剂量下有效,降低雌性和雄性虫体负担的幅度分别为 95%和 80%。在各种发育时间点(1、7、15、21 和/或 42 天龄),单次口服 400 和/或 600mg/kg 剂量与 QDx4 数据一致;一旦寄生虫完成肺迁移,疗效最强,雌性和雄性虫体负担至少降低 90%和 80%。在体外,TPT 硫酸盐对寄生虫无活性,提示其具有前药作用机制。在小鼠中,TPT 硫酸盐被完全吸收,并经历快速、非 CYP 介导的首过代谢,该代谢由脱硫作用引发,并产生一系列代谢物。最初形成的含有游离巯基的代谢物,称为 TP 硫醇,通过化学合成得到;它在体外剂量依赖性地降低曼氏血吸虫和埃及血吸虫的运动能力。此外,当作为单次 50mg/kg IP 剂量给药时,TP 硫醇可使 33 日龄曼氏血吸虫雌性和雄性虫体负担分别降低 35%和 44%,同时器官肿大程度较轻。总的来说,TPT 硫酸盐的疗效与 PZQ 相当。此外,寄生虫杀灭代谢物的特征有助于理解和改进化学性质,并确定作用机制和/或靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a29/6287543/be07ff52fb53/fx1.jpg

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