Therapeutic activity of eugenol towards mitigation of anaemia and oxidative organ damage caused by Plasmodium berghei

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mukhtar Adeiza Suleiman, Mohammed Aliyu Usman, Samson Olayinka Awogbamila, Umar Adam Idris, Fatima Binta Ibrahim, Halimat-Oyibo Mohammed
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Abstract

The parasite responsible for causing malaria infection, Plasmodium, is known to exhibit resistance to a number of already available treatments. This has prompted the continue search for new antimalarial drugs ranging from medicinal plant parts to synthetic compounds. In lieu of this, the mitigative action of the bioactive compound, eugenol towards P. berghei-induced anaemia and oxidative organ damage was investigated following a demonstration of in vitro and in vivo antiplasmodial effects. Mice were infected with chloroquine-sensitive strain of P. berghei and thereafter treated with eugenol at doses of 10 and 20 mg/kg body weight (BW) for seven days. The packed cell volume and redox sensitive biomarkers in the liver, brain and spleen were measured. Our result demonstrated that eugenol significantly (p < 0.05) ameliorated the P. berghei-associated anaemia at a dose of 10 mg/kg BW. In addition, the compound, at a dose of 10 mg/kg BW, significantly (p < 0.05) alleviated the P. berghei-induced organ damage. This evidently confirmed that eugenol plays an ameliorative role towards P. berghei-related pathological alterations. Hence, the study opens up a new therapeutic use of eugenol against plasmodium parasite.

Abstract Image

丁香酚对伯氏疟原虫引起的贫血和氧化性器官损伤的治疗作用
众所周知,导致疟疾感染的寄生虫疟原虫对许多现有的治疗方法表现出耐药性。这促使人们继续寻找新的抗疟药物,从药用植物部分到合成化合物。取而代之的是,在体外和体内抗疟原虫作用的证明后,研究了生物活性化合物丁香酚对伯氏疟原虫诱导的贫血和氧化性器官损伤的缓解作用。用对氯喹敏感的伯氏疟原虫菌株感染小鼠,然后用丁香酚以10和20mg/kg体重(BW)的剂量治疗7天。测量了肝脏、大脑和脾脏中的堆积细胞体积和氧化还原敏感生物标志物。我们的结果表明,丁香酚在10mg/kg BW的剂量下显著(p<0.05)改善了p.berghei相关的贫血。此外,该化合物在10mg/kg体重的剂量下,显著(p>0.05)减轻了p.berghei诱导的器官损伤。这显然证实了丁香酚对伯氏疟原虫相关的病理改变具有改善作用。因此,该研究开辟了丁香酚治疗疟原虫的新用途。
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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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