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核苷类似物 GS-441524 能在组织培养和实验猫感染研究中强烈抑制猫传染性腹膜炎(FIP)病毒。

The nucleoside analog GS-441524 strongly inhibits feline infectious peritonitis (FIP) virus in tissue culture and experimental cat infection studies.

机构信息

Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA.

Gilead Sciences, Foster City, CA, USA.

出版信息

Vet Microbiol. 2018 Jun;219:226-233. doi: 10.1016/j.vetmic.2018.04.026. Epub 2018 Apr 22.

Abstract

Feline infectious peritonitis (FIP) is a common and highly lethal coronavirus disease of domestic cats. Recent studies of diseases caused by several RNA viruses in people and other species indicate that antiviral therapy may be effective against FIP in cats. The small molecule nucleoside analog GS-441524 is a molecular precursor to a pharmacologically active nucleoside triphosphate molecule. These analogs act as an alternative substrate and RNA-chain terminator of viral RNA dependent RNA polymerase. We determined that GS-441524 was non-toxic in feline cells at concentrations as high as 100 uM and effectively inhibited FIPV replication in cultured CRFK cells and in naturally infected feline peritoneal macrophages at concentrations as low as 1 uM. We determined the pharmacokinetics of GS-441524 in cats in vivo and established a dosage that would sustain effective blood levels for 24 h. In an experimental FIPV infection of cats, GS-441524 treatment caused a rapid reversal of disease signs and return to normality with as little as two weeks of treatment in 10/10 cats and with no apparent toxicity.

摘要

猫传染性腹膜炎(FIP)是一种常见且高度致命的猫冠状病毒病。最近对人和其他物种的几种 RNA 病毒引起的疾病的研究表明,抗病毒疗法可能对猫的 FIP 有效。小分子核苷类似物 GS-441524 是一种具有药理活性的核苷三磷酸分子的前体分子。这些类似物可作为病毒 RNA 依赖性 RNA 聚合酶的替代底物和 RNA 链终止子。我们确定,GS-441524 在高达 100µM 的浓度下对猫细胞无毒,并且在浓度低至 1µM 时即可有效抑制培养的 CRFK 细胞和自然感染的猫腹腔巨噬细胞中的 FIPV 复制。我们在体内确定了 GS-441524 在猫中的药代动力学,并建立了一个剂量,该剂量可维持 24 小时的有效血药水平。在猫的实验性 FIPV 感染中,GS-441524 治疗可迅速逆转疾病迹象,并使 10/10 只猫在短短两周的治疗后恢复正常,且无明显毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495a/7117434/8d5fe1228738/gr1_lrg.jpg

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