Department of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, Thailand.
Research Center in Tropical Pathobiology, Walailak University, Nakhon Si Thammarat, 80160, Thailand.
BMC Complement Med Ther. 2023 Sep 20;23(1):332. doi: 10.1186/s12906-023-04150-1.
Cerebral malaria is one of the most serious complications of Plasmodium infection and causes behavioral changes. However, current antimalarial drugs have shown poor outcomes. Therefore, new antimalarials with neuroprotective effects are urgently needed. This study aimed to evaluate the effects of selected extracts as monotherapy or adjunctive therapy with artesunate on antimalarial, anti-inflammatory, antioxidant, and neuroprotective properties in experimental cerebral malaria (ECM).
ECM was induced in male C57BL/6 mice by infection with Plasmodium berghei ANKA (PbA). Ethanolic extracts of Atractylodes lancea (a dose of 400 mg/kg) and Prabchompoothaweep remedy (a dose of 600 mg/kg) were evaluated as monotherapy and adjunctive therapy combined with artesunate at the onset of signs of cerebral malaria and continued for 7 consecutive days. Parasitemia, clinical scores, and body weight were recorded throughout the study. At day 13 post-infection, mouse brains were dissected and processed for the study of the inflammatory response, oxidative stress, blood-brain barrier (BBB) integrity, histopathological changes, and neurocognitive impairments.
Ethanolic extracts of A. lancea and Prabchompoothaweep remedy alone improved cerebral malaria outcome in ECM, whereas artesunate combined with extracts of A. lancea or Prabchompoothaweep remedy significantly improved the outcome of artesunate and crude extracts alone. Using real-time PCR, PbA-infected mice that had received the combination treatment showed significantly reduced gene expression of inflammatory cytokines (TNF-α, IL-1β, IL-6, and IL-10), chemokines (CXCL4 and CXCL10), and adhesion molecules (ICAM-1, VCAM1, and CD36). The PbA-infected mice that received the combination treatment showed a significantly decreased malondialdehyde level compared to the untreated group. Similarly, the Evans blue dye assay revealed significantly less dye extravasation in the brains of infected mice administered the combination treatment, indicating improved BBB integrity. Combination treatment improved survival and reduced pathology in the PbA-infected group. Additionally, combination treatment resulted in a significantly reduced level of cognitive impairment, which was analyzed using a novel object recognition test.
This study demonstrated that artesunate combined with A. lancea or Prabchompoothaweep remedy extracts as adjunctive therapy reduced mortality, neuroinflammation, oxidative stress, BBB integrity protection, and neurocognitive impairment in the ECM.
脑型疟疾是恶性疟原虫感染最严重的并发症之一,可导致行为改变。然而,目前的抗疟药物疗效不佳。因此,急需具有神经保护作用的新型抗疟药物。本研究旨在评估所选提取物作为单一疗法或与青蒿琥酯联合治疗实验性脑型疟疾(ECM)的抗疟、抗炎、抗氧化和神经保护作用。
通过感染伯氏疟原虫 ANKA(PbA)诱导雄性 C57BL/6 小鼠发生 ECM。评估苍术(剂量为 400mg/kg)和 Prabchompoothaweep 补救剂(剂量为 600mg/kg)的乙醇提取物作为单一疗法和联合青蒿琥酯治疗,在出现脑型疟疾迹象时开始治疗,连续治疗 7 天。整个研究过程中记录寄生虫血症、临床评分和体重。感染后第 13 天,剖脑并进行炎症反应、氧化应激、血脑屏障(BBB)完整性、组织病理学变化和神经认知障碍研究。
苍术和 Prabchompoothaweep 补救剂的乙醇提取物单独使用可改善 ECM 中的脑型疟疾结局,而青蒿琥酯联合苍术或 Prabchompoothaweep 补救剂提取物可显著改善青蒿琥酯和粗提取物单独使用的结局。通过实时 PCR,接受联合治疗的 PbA 感染小鼠的炎症细胞因子(TNF-α、IL-1β、IL-6 和 IL-10)、趋化因子(CXCL4 和 CXCL10)和粘附分子(ICAM-1、VCAM1 和 CD36)的基因表达明显降低。与未治疗组相比,接受联合治疗的 PbA 感染小鼠的丙二醛水平明显降低。同样,伊文思蓝染料试验显示,接受联合治疗的感染小鼠脑内染料外渗明显减少,表明 BBB 完整性得到改善。联合治疗提高了 PbA 感染组的生存率并减轻了病理变化。此外,联合治疗可显著降低新型物体识别试验分析的认知障碍水平。
本研究表明,青蒿琥酯联合苍术或 Prabchompoothaweep 补救剂提取物作为辅助治疗可降低 ECM 中的死亡率、神经炎症、氧化应激、BBB 完整性保护和神经认知障碍。