Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Boehringer Ingelheim Pharma, Biberach, Germany.
Lett Appl Microbiol. 2020 Nov;71(5):542-549. doi: 10.1111/lam.13366. Epub 2020 Sep 11.
Malaria is a worldwide serious-threatening infectious disease caused by Plasmodium and the parasite resistance to antimalarial drugs has confirmed a significant obstacle to novel therapeutic antimalarial drugs. In this article, we assessed the antioxidant and anti-inflammatory activity of nanoparticles prepared from Indigofera oblongifolia extract (AgNPs) against the infection with Plasmodium chabaudi caused in mice spleen. AgNPs could significantly suppress the parasitaemia caused by the parasite to approximately 98% on day 7 postinfection with P. chabaudi and could improve the histopathological induced spleen damage. Also, AgNPs were able to increase the capsule thickness of the infected mice spleen. In addition, the AgNPs functioned as an antioxidant agent that affects the change in glutathione, nitric oxide and catalase levels in the spleen. Moreover spleen IL1β, IL-6 and TNF-α-mRNA expression was regulated by AgNPs administration to the infected mice. These results indicated the anti-oxidant and the anti-inflammatory protective role of AgNPs against P. chabaudi-induced spleen injury.
疟疾是一种全球性的严重威胁传染病,由疟原虫引起,寄生虫对抗疟药物的耐药性已成为新型抗疟药物的重大障碍。在本文中,我们评估了从菘蓝提取物中制备的纳米粒子(AgNPs)对感染伯氏疟原虫引起的小鼠脾脏的抗氧化和抗炎活性。AgNPs 可显著抑制感染伯氏疟原虫后第 7 天的寄生虫血症,约为 98%,并可改善寄生虫诱导的脾损伤的组织病理学变化。此外,AgNPs 能够增加感染小鼠脾脏的囊厚度。此外,AgNPs 作为一种抗氧化剂,影响谷胱甘肽、一氧化氮和过氧化氢酶水平在脾中的变化。此外,AgNPs 给药还可调节感染小鼠脾中 IL1β、IL-6 和 TNF-α-mRNA 的表达。这些结果表明,AgNPs 对抗伯氏疟原虫诱导的脾损伤具有抗氧化和抗炎保护作用。