Atanu Francis O, Idih Favour M, Nwonuma Charles O, Hetta Helal F, Alamery Salman, El-Saber Batiha Gaber
Department of Biochemistry, Faculty of Natural Sciences, Kogi State University, P.M.B. 1008, Anyigba, Nigeria.
Department of Biochemistry, Faculty of Pure and Applied Sciences, Landmark University, Omu-Aran, Kwara State, Nigeria.
Evid Based Complement Alternat Med. 2021 Oct 6;2021:2599191. doi: 10.1155/2021/2599191. eCollection 2021.
Extracts of and are used in herbal medicine for the treatment of malaria. This work investigated the phytochemical, antioxidant, and antimalarial effects of hydromethanolic extracts of and . A four-day chemosuppressive test was conducted to assess the ability of the extracts to prevent establishment of infection. Three doses of the extracts were administered-100, 200, and 400 mg/kg bw-prior to challenge. Change in body weight, parasitemia, packed cell volume (PCV), and mean survival time was determined. A three-day curative test was also carried out on -infected mice to determine the effects of the plant extracts (200 mg/kg bw) on parasitemia and biochemical indices of liver and kidney functions, lipid metabolism, and oxidative stress. The study revealed that the extracts possessed phenolic compounds (34.13 ± 1.90 mg GAE/g for and 27.99 ± 1.46 mg GAE/g for ) and flavonoids (19.47 ± 1.89 mg QE/g for and 18.24 ± 1.36 mg QE/g for ). antioxidant activity measured as total antioxidant power, total reducing power, and DPPH radical scavenging activity showed that the extracts possessed higher antioxidant activity than the reference compounds. The outcome of the chemosuppressive test revealed that whereas -infected mice had high parasitemia, decreased mean survival time, exhibited loss of weight, and had low PCV, treatment with the extracts reversed the effects in a concentration-dependent manner. Similarly, the curative test revealed that the extracts significantly suppressed parasitemia compared with the malaria negative control group. This was mirrored by reversal of indices of hepatic toxicity (AST, ALT, and ALP levels), nephropathy (urea and creatinine levels), oxidative stress (SOD, CAT, GPx, GSH, and lipid peroxides), and dyslipidemia (TC, HDL, and TG levels and HMG-CoA reductase activity) in infected but treated mice compared with negative control. Put together, the results of this study demonstrate that the extracts of and possess antimalarial properties and are able to ameliorate metabolic dysregulations that characterize infection. The phytoconstituents in these extracts are believed to be responsible for the pharmacological activity reported in this study.
[植物名称1]和[植物名称2]的提取物被用于草药医学中治疗疟疾。本研究调查了[植物名称1]和[植物名称2]的氢甲醇提取物的植物化学、抗氧化和抗疟作用。进行了为期四天的化学抑制试验,以评估提取物预防感染建立的能力。在疟原虫攻击前,给予三种剂量的提取物——100、200和400mg/kg体重。测定体重、寄生虫血症、红细胞压积(PCV)和平均存活时间的变化。还对感染疟原虫的小鼠进行了为期三天的治疗试验,以确定植物提取物(200mg/kg体重)对寄生虫血症以及肝功能、肾功能、脂质代谢和氧化应激的生化指标的影响。研究表明,提取物含有酚类化合物([植物名称1]为34.13±1.90mg GAE/g,[植物名称2]为27.99±1.46mg GAE/g)和黄酮类化合物([植物名称1]为19.47±1.89mg QE/g,[植物名称2]为18.24±1.36mg QE/g)。以总抗氧化能力、总还原能力和DPPH自由基清除活性衡量的抗氧化活性表明,提取物具有比参考化合物更高的抗氧化活性。化学抑制试验的结果显示,感染疟原虫的小鼠寄生虫血症高、平均存活时间缩短、体重减轻且红细胞压积低,而用提取物治疗以浓度依赖的方式逆转了这些影响。同样,治疗试验表明,与疟疾阴性对照组相比,提取物显著抑制了寄生虫血症。与阴性对照组相比,感染但经治疗的小鼠肝毒性指标(AST、ALT和ALP水平)、肾病指标(尿素和肌酐水平)、氧化应激指标(SOD、CAT、GPx、GSH和脂质过氧化物)以及血脂异常指标(TC、HDL和TG水平以及HMG-CoA还原酶活性)的逆转反映了这一点。综上所述,本研究结果表明,[植物名称1]和[植物名称2]的提取物具有抗疟特性,并且能够改善疟原虫感染所特有的代谢失调。这些提取物中的植物成分被认为是本研究中报道的药理活性的原因。