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首页> 外文期刊>International Journal for Parasitology: Drugs and Drug Resistance >Safety and efficacy of the bumped kinase inhibitor BKI-1553 in pregnant sheep experimentally infected with Neospora caninum tachyzoites
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Safety and efficacy of the bumped kinase inhibitor BKI-1553 in pregnant sheep experimentally infected with Neospora caninum tachyzoites

机译:颠簸激酶抑制剂BKI-1553在实验感染新孢子虫速殖子的怀孕绵羊中的安全性和有效性

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Neospora caninum is one of the main causes of abortion in cattle, and recent studies have highlighted its relevance as an abortifacient in small ruminants. Vaccines or drugs for the control of neosporosis are lacking. Bumped kinase inhibitors (BKIs), which are ATP-competitive inhibitors of calcium dependent protein kinase 1 (CDPK1), were shown to be highly efficacious against several apicomplexan parasites in vitro and in laboratory animal models. We here present the pharmacokinetics, safety and efficacy of BKI-1553 in pregnant ewes and foetuses using a pregnant sheep model of N. caninum infection. BKI-1553 showed exposure in pregnant ewes with trough concentrations of approximately 4?μM, and of 1 μM in foetuses. Subcutaneous BKI-1553 administration increased rectal temperatures shortly after treatment, and resulted in dermal nodules triggering a slight monocytosis after repeated doses at short intervals. BKI-1553 treatment decreased fever in infected pregnant ewes already after two applications, resulted in a 37–50% reduction in foetal mortality, and modulated immune responses; IFNγ levels were increased early after infection and IgG levels were reduced subsequently. N. caninum was abundantly found in placental tissues; however, parasite detection in foetal brain tissue decreased from 94% in the infected/untreated group to 69–71% in the treated groups. In summary, BKI-1553 confers partial protection against abortion in a ruminant experimental model of N. caninum infection during pregnancy. In addition, reduced parasite detection, parasite load and lesions in foetal brains were observed.
机译:犬新孢子虫是牛流产的主要原因之一,最近的研究强调了其作为小反刍动物流产的相关性。缺乏用于控制新孢子虫病的疫苗或药物。颠簸激酶抑制剂(BKIs)是钙依赖性蛋白激酶1(CDPK1)的ATP竞争性抑制剂,在体外和实验室动物模型中显示出对几种apiplexplexan寄生虫的高效杀伤力。我们在这里介绍使用犬新孢子虫感染的妊娠绵羊模型,BKI-1553在妊娠母羊和胎儿中的药代动力学,安全性和有效性。 BKI-1553在怀孕母羊中的接触谷浓度约为4?μM,在胎儿中则为1μM。皮下注射BKI-1553在治疗后不久会升高直肠温度,并导致皮肤结节在短时间内重复给药后触发轻微的单核细胞增多。 BKI-1553治疗在两次应用后已经降低了感染母羊的发烧,导致胎儿死亡率降低了37-50%,并调节了免疫反应。感染后早期IFNγ水平升高,随后IgG水平降低。在胎盘组织中广泛发现犬新孢子虫。然而,胎儿脑组织中的寄生虫检出率从感染/未治疗组的94%降至治疗组的69-71%。总而言之,BKI-1553在妊娠期间的犬新孢子虫感染的反刍动物实验模型中提供了部分保护以防止流产。另外,观察到胎儿脑中的寄生虫检测,寄生虫负荷和损伤减少。

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