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左旋咪唑对……的杀线虫作用及细胞毒性

Nematicidal Effects and Cytotoxicity of Levamisole on .

作者信息

Han Zhengxuan, Zhong Yipeng, Chen Ni, Liu Zichen, Yuan Zhankui, Jin Yipeng

机构信息

College of Veterinary Medicine, China Agricultural University, Yuanmingyuan West Road 2, Haidian District, Beijing 100193, China.

College of Veterinary Medicine, Nanjing Agricultural University, Chinese Nanjing Weigang No. 1, Nanjing 210095, China.

出版信息

Animals (Basel). 2025 May 26;15(11):1551. doi: 10.3390/ani15111551.

Abstract

() is a zoonotic ocular parasite that poses a public health risk. Current treatment depends on mechanical parasite extraction and specific prophylactic anthelmintics, but direct ocular deworming agents are limited and expensive, and mechanical removal is often incomplete, causing animal stress and ocular injury. Levamisole eye drops have been applied; however, their efficacy and safety remain undefined. We established a standardized viability assessment system (TVAS) and an animal infection model to evaluate candidate drugs. In vivo, 5 mg/mL levamisole was administered at escalating frequencies. Ocular symptoms, complete blood count (CBC), and serum biochemistry were measured, and cytotoxicity was assessed using Cell Counting Kit-8 (CCK-8) and lactate dehydrogenase (LDH) assays on rabbit conjunctival epithelial cells (RCECs).Four doses of 5 mg/mL levamisole applied at 30 min intervals cleared from infected eyes within 2 h without significant changes in CBC, serum biochemistry, or ocular symptom scores. CCK-8 and LDH assays indicated minimal cytotoxicity in RCECs within 4 h. However, prolonged exposure (6-12 h) led to a significant decrease in RCEC viability, suggesting potential cytotoxicity with extended use and highlighting the need for further safety evaluation. A regimen of four topical administrations of 5 mg/mL levamisole at 30 min intervals cleared from infected eyes with minimal cytotoxicity, supporting its safety and efficacy as a topical treatment.

摘要

(某寄生虫名)是一种人畜共患的眼部寄生虫,对公众健康构成风险。目前的治疗方法依赖于机械性地摘除寄生虫以及使用特定的预防性驱虫药,但直接用于眼部的驱虫剂有限且昂贵,而且机械清除往往不彻底,会给动物带来应激并造成眼部损伤。已应用了左旋咪唑滴眼液;然而,其疗效和安全性尚不明确。我们建立了一个标准化的活力评估系统(TVAS)和一个动物感染模型来评估候选药物。在体内实验中,以递增频率给予5mg/mL的左旋咪唑。测量眼部症状、全血细胞计数(CBC)和血清生化指标,并使用细胞计数试剂盒-8(CCK-8)和乳酸脱氢酶(LDH)检测法对兔结膜上皮细胞(RCEC)进行细胞毒性评估。每隔30分钟给予四剂5mg/mL的左旋咪唑,在2小时内可清除感染眼中的寄生虫,且CBC、血清生化指标或眼部症状评分无显著变化。CCK-8和LDH检测表明,在4小时内RCEC的细胞毒性最小。然而,长时间暴露(6 - 12小时)会导致RCEC活力显著下降,这表明长期使用可能存在细胞毒性,凸显了进一步进行安全性评估的必要性。每隔30分钟局部给予四剂5mg/mL左旋咪唑的方案可清除感染眼中的寄生虫,且细胞毒性最小,这支持了其作为局部治疗的安全性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc1/12153631/f6253617e92b/animals-15-01551-g002.jpg

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