紫苏醇治疗柔嫩艾美耳球虫感染的疗效评价

IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qingyang Song , Yihao Yu , Shujing Wang , Hongmei Li , Xiaomin Zhao , Ningning Zhao , Xiao Zhang
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引用次数: 0

摘要

最近,由于对新型抗寄生虫药物的广泛使用日益关注,人们越来越关注开发既高效又低毒性的新型抗寄生虫药物。天然产物因其多样的生物活性和最小的副作用而引起了人们的极大兴趣。本研究对紫苏醇、香芹酮、薄荷酮和紫苏醛四种紫苏科植物化合物的抗艾美耳球虫活性进行了研究。我们的体外实验表明,这四种化合物,特别是紫苏醇,对柔嫩芽胞杆菌卵囊的孢子形成具有有效的抑制作用。此外,我们的体内试验显示,以200 mg/kg的剂量用这四种化合物治疗可显著减少卵囊脱落、盲肠病变和由tenella感染引起的体重减轻,从而显示出适度的抗e。tenella活动。紫苏醇的抗球虫指数(ACI)为161.4,效果最好。综上所述,我们的研究结果表明,这四种来自Lamiaceae家族的化合物具有抗e。在体外和体内,紫苏醇对E. tenella表现出特别强大的抑制作用。其作用机制和潜在的治疗应用值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the efficacy of Perillyl alcohol in the treatment of Eimeria tenella infection
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.
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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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