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反式二氢查耳酮和 4 水合查耳酮对巴贝西虫和泰勒虫生长的影响。

The effects of trans-chalcone and chalcone 4 hydrate on the growth of Babesia and Theileria.

机构信息

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido, Japan.

Department of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour, AlBeheira, Egypt.

出版信息

PLoS Negl Trop Dis. 2019 May 24;13(5):e0007030. doi: 10.1371/journal.pntd.0007030. eCollection 2019 May.

Abstract

BACKGROUND

Chemotherapy is a principle tool for the control and prevention of piroplasmosis. The search for a new chemotherapy against Babesia and Theileria parasites has become increasingly urgent due to the toxic side effects of and developed resistance to the current drugs. Chalcones have attracted much attention due to their diverse biological activities. With the aim to discover new drugs and drug targets, in vitro and in vivo antibabesial activity of trans-chalcone (TC) and chalcone 4 hydrate (CH) alone and combined with diminazene aceturate (DA), clofazimine (CF) and atovaquone (AQ) were investigated.

METHODOLOGY/PRINCIPAL FINDINGS: The fluorescence-based assay was used for evaluating the inhibitory effect of TC and CH on four Babesia species, including B. bovis, B. bigemina, B. divergens, B. caballi, and T. equi, the combination with DA, CF, and AQ on in vitro cultures, and on the multiplication of a B. microti-infected mouse model. The cytotoxicity of compounds was tested on Madin-Darby bovine kidney (MDBK), mouse embryonic fibroblast (NIH/3T3), and human foreskin fibroblast (HFF) cell lines. The half maximal inhibitory concentration (IC50) values of TC and CH against B. bovis, B. bigemina, B. divergens, B. caballi, and T. equi were 69.6 ± 2.3, 33.3 ± 1.2, 64.8 ± 2.5, 18.9 ± 1.7, and 14.3 ± 1.6 μM and 138.4 ± 4.4, 60.9 ± 1.1, 82.3 ± 2.3, 27.9 ± 1.2, and 19.2 ± 1.5 μM, respectively. In toxicity assays, TC and CH affected the viability of MDBK, NIH/3T3, and HFF cell lines the with half maximum effective concentration (EC50) values of 293.9 ± 2.9, 434.4 ± 2.7, and 498 ± 3.1 μM and 252.7 ± 1.7, 406.3 ± 9.7, and 466 ± 5.7 μM, respectively. In the mouse experiment, TC reduced the peak parasitemia of B. microti by 71.8% when administered intraperitoneally at 25 mg/kg. Combination therapies of TC-DA and TC-CF were more potent against B. microti infection in mice than their monotherapies.

CONCLUSIONS/SIGNIFICANCE: In conclusion, both TC and CH inhibited the growth of Babesia and Theileria in vitro, and TC inhibited the growth of B. microti in vivo. Therefore, TC and CH could be candidates for the treatment of piroplasmosis after further studies.

摘要

背景

化疗是控制和预防梨形虫病的主要手段。由于当前药物的毒性副作用和耐药性的出现,寻找新的抗巴贝斯虫和泰勒虫的化疗药物变得越来越紧迫。查耳酮因其多样的生物活性而受到广泛关注。为了发现新的药物和药物靶点,我们研究了反式查耳酮(TC)和查耳酮 4 水合物(CH)单独以及与二甲氮嗪(DA)、氯法齐明(CF)和阿托伐醌(AQ)联合对四种巴贝斯虫的体外和体内抗巴贝斯虫活性,包括牛巴贝斯虫、双芽巴贝斯虫、分歧巴贝斯虫、马巴贝斯虫和马泰勒虫。

方法/主要发现:荧光测定法用于评估 TC 和 CH 对四种巴贝斯虫(牛巴贝斯虫、双芽巴贝斯虫、分歧巴贝斯虫、马巴贝斯虫和马泰勒虫)的抑制作用,DA、CF 和 AQ 对体外培养物和 B. microti 感染小鼠模型的增殖的联合作用。在 Madin-Darby 牛肾(MDBK)、小鼠胚胎成纤维细胞(NIH/3T3)和人包皮成纤维细胞(HFF)细胞系中测试化合物的细胞毒性。TC 和 CH 对 B. bovis、B. bigemina、B. divergens、B. caballi 和 T. equi 的半最大抑制浓度(IC50)值分别为 69.6±2.3、33.3±1.2、64.8±2.5、18.9±1.7 和 14.3±1.6 μM 和 138.4±4.4、60.9±1.1、82.3±2.3、27.9±1.2 和 19.2±1.5 μM。在毒性试验中,TC 和 CH 影响 MDBK、NIH/3T3 和 HFF 细胞系的活力,其半最大有效浓度(EC50)值分别为 293.9±2.9、434.4±2.7 和 498±3.1 μM 和 252.7±1.7、406.3±9.7 和 466±5.7 μM。在小鼠实验中,当腹腔内给予 25 mg/kg 的 TC 时,可使 B. microti 的峰值寄生虫血症减少 71.8%。TC-DA 和 TC-CF 的联合治疗比单独治疗更能有效抑制小鼠体内的 B. microti 感染。

结论

总之,TC 和 CH 均能抑制体外巴贝斯虫和泰勒虫的生长,TC 能抑制体内 B. microti 的生长。因此,TC 和 CH 可能是进一步研究后治疗梨形虫病的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6215/6534319/b21492679301/pntd.0007030.g001.jpg

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