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睡茄 NMITLI - 101R、118R 化学型和醉茄素 A 对实验内脏利什曼病的疗效。

Efficacy of Withania somnifera chemotypes NMITLI - 101R, 118R and Withaferin A against experimental visceral leishmaniasis.

机构信息

Division of Parasitology, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.

出版信息

Parasite Immunol. 2014 Jun;36(6):253-65. doi: 10.1111/pim.12112.

DOI:10.1111/pim.12112
PMID:24830833
Abstract

The immunoprophylactic and therapeutic potentials of root extracts of Withania somnifera chemotypes (NMITLI-118, NMITLI-101) and pure withanolide-withaferin A was investigated against Leishmania donovani infection in hamsters. The naive animals, fed orally with immunostimulatory doses of chemotypes 101R, 118R (10 and 3 mg/kg) and withaferin A (9 and 3 mg/kg) for five consecutive days and challenged with Leishmania parasites on day 6, were euthanized on days 30 and 45 p.c. for the assessment of parasite clearance, real-time analysis of mRNAs of Th1/Th2 cytokines (IFN-γ, IL-12, TNF-α, iNOS/IL-4, IL-10 and TGF-β), NO production, reactive oxygen species (ROS) generation, lymphocyte transformation test and antibody responses. By day 45 p.c., there was a significant increase in the mRNA expression of iNOS, IFN-γ, IL-12 and TNF-α but decrease in IL-4, IL-10 and TGF-β, an enhanced Leishmania-specific LTT response as well as ROS, NO and antileishmanial IgG2 levels in 101R-treated hamsters followed by 118R- and withaferin A-treated ones, respectively. When these chemotypes were given to L. donovani-infected hamsters at different doses, there was moderate therapeutic efficacy of chemotype 101R (~50%) at 30 mg/kg × 5 followed by the other two. The results established that the 101R is the most potential chemotype and can be evaluated for combination therapy along with available antileishmanials.

摘要

我们研究了睡茄化学型(NMITLI-118、NMITLI-101)根提取物和纯生物堿-醉茄堿 A 的免疫预防和治疗潜力,以对抗感染仓鼠的利什曼原虫。在连续 5 天口服免疫刺激剂量的化学型 101R、118R(10 和 3mg/kg)和醉茄堿 A(9 和 3mg/kg)后,未感染的动物于第 6 天受到利什曼原虫寄生虫的攻击,并在第 30 和 45 天进行安乐死,以评估寄生虫清除率、Th1/Th2 细胞因子(IFN-γ、IL-12、TNF-α、iNOS/IL-4、IL-10 和 TGF-β)的实时分析、NO 产生、活性氧(ROS)生成、淋巴细胞转化试验和抗体反应。在第 45 天,101R 处理的仓鼠中 iNOS、IFN-γ、IL-12 和 TNF-α 的 mRNA 表达显著增加,而 IL-4、IL-10 和 TGF-β 减少,利什曼原虫特异性 LTT 反应以及 ROS、NO 和抗利什曼原虫 IgG2 水平增强,随后是 118R 和醉茄堿 A 处理的仓鼠。当这些化学型以不同剂量给予感染利什曼原虫的仓鼠时,化学型 101R(30mg/kg×5)具有中度的治疗效果,其次是其他两种。结果表明,101R 是最有潜力的化学型,可以与现有的抗利什曼原虫药物联合评估用于治疗。

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