Qingyang Song , Yihao Yu , Shujing Wang , Hongmei Li , Xiaomin Zhao , Ningning Zhao , Xiao Zhang
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引用次数: 0
Abstract
Recently, there has been an increased focus on the development of novel anti-parasitic drugs that exhibit both highly efficacy and low toxicity due to growing concerns associated with the widespread use of such drugs. Natural products have garnered significant interest owing to their diverse biological activities and minimal adverse effects. In this study, we assessed the anti-Eimeria tenella activity of four plant compounds belonging to the Lamiaceae family, namely Perillyl alcohol, Carvone, Menthone and Perilla aldehyde. Our in vitro experiments demonstrated that all four compounds, particularly Perillyl alcohol, exhibited potent inhibition against sporulation formation of E. tenella oocyst. Furthermore, our in vivo tests revealed that treatment with these four compounds at a dose of 200 mg/kg significantly reduced oocyst shedding as well as cecal lesions and weight loss caused by E. tenella infection, thereby demonstrating moderate anti-E. tenella activity. Notably, Perillyl alcohol displayed the highest efficacy against E. tenella with an anticoccidial index (ACI) value of 161.4. In summary, our findings indicate that these four compounds derived from the Lamiaceae family exhibit anti-E. tenella activity both in vitro and in vivo, with Perillyl alcohol displaying particularly robust inhibitory effects on E. tenella. It is worthy of further investigation to explore its mechanism of action and potential therapeutic applications.
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.