Kevin Tako Djimefo Alex, Cedric Yamssi, Nadia Noumedem Anangmo Christelle, Sandra Tientcheu Noutong Jemimah, Azizi Mounvera Abdel, Sidiki Ngouyamsa Nsapkain Aboubakar, Guy-Armand Gamago Nkadeu, Christian Mbohou Nchetnkou, Géraldine Essangui Same Estelle, Roméo Tankoua-Tchounda, Payne Vincent Khan, Gustave Lehman Léopold
Department of Animal Organisms, Faculty of Science, University of Douala, P.O. Box 24157, Douala, Cameroon.
Laboratory of Tropical and Emerging Infectious Diseases, Dschang, Cameroon.
J Parasitol Res. 2024 Mar 25;2024:8821019. doi: 10.1155/2024/8821019. eCollection 2024.
The spread of drug resistance is a significant issue, particularly in endemic countries with limited resources. The aim of this study was to evaluate antimalarial and antioxidant activity of in order to justify its use in traditional medicine.
Evaluation of the antimalarial activity of was carried out according to the model of the suppressive and curative test of Peters' over 4 days in infected mice. Antioxidant parameters and stress were measured after intraperitoneal administration of 1 × 10 infected red blood cells.
At doses of 150 mg/kg, 300 mg/kg, and 600 mg/kg, administration of B. micrantha substantially produced suppression of infection by 67.75%, 73.46%, and 78.99%, respectively, while 84.64% of the untreated group (1% DMSO) had suppression from chloroquine. The curative test significantly decreased the levels of parasitaemia and death in the treated groups. Furthermore, after extract was given to infected mice, a noteworthy increase in total protein, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) was observed. On the other hand, hepatic catalase (CAT) and superoxide dismutase (SOD) productions were considerably greater than that of the healthy control. Mice had considerably lower levels of nonenzymatic antioxidant markers such as glutathione, NO, and MDA showing that the liver was protected.
The infected groups responded favorably to the ethanol extract of . This result justifies investigation for its use in Cameroon.
耐药性的传播是一个重大问题,尤其是在资源有限的流行国家。本研究的目的是评估[植物名称未给出]的抗疟和抗氧化活性,以证明其在传统医学中的应用合理性。
根据彼得斯在感染[动物名称未给出]小鼠身上进行的4天抑制和治疗试验模型,评估[植物名称未给出]的抗疟活性。在腹腔注射1×10个感染的红细胞后,测量抗氧化参数和应激反应。
在150mg/kg、300mg/kg和600mg/kg的剂量下,小花[植物名称未给出]的给药分别使[感染名称未给出]感染的抑制率大幅达到67.75%、73.46%和78.99%,而未治疗组(1%DMSO)有84.64%的抑制率来自氯喹。治疗试验显著降低了治疗组的寄生虫血症水平和死亡率。此外,在给感染小鼠服用[植物名称未给出]提取物后,观察到总蛋白、天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)有显著增加。另一方面,肝脏过氧化氢酶(CAT)和超氧化物歧化酶(SOD)的产生明显高于健康对照组。小鼠的非酶抗氧化标志物如谷胱甘肽、一氧化氮和丙二醛水平显著较低,表明肝脏得到了保护。
感染组对[植物名称未给出]的乙醇提取物反应良好。这一结果证明了在喀麦隆对其进行应用研究的合理性。