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大麻二酚对替米考星人体毒性的保护作用——体外研究

Protective Action of Cannabidiol on Tiamulin Toxicity in Humans-In Vitro Study.

作者信息

Pankowska Eryka, Kończak Oliwia, Żakowicz Paula, Wojciechowicz Tatiana, Gogulski Maciej, Radko Lidia

机构信息

Students Scientific Society of Veterinary Medicine, Section of Veterinary Pharmacology and Toxicology "Paracelsus", Faculty of Veterinary Medicine and Animal Sciences, Poznan University of Life Sciences, 60-637 Poznan, Poland.

Department of Animal Physiology, Biochemistry and Biostructure, Faculty of Veterinary Medicine and Animal Sciences, Poznan University of Life Sciences, 60-637 Poznan, Poland.

出版信息

Int J Mol Sci. 2024 Dec 18;25(24):13542. doi: 10.3390/ijms252413542.

Abstract

The growing awareness and need to protect public health, including food safety, require a thorough study of the mechanism of action of veterinary drugs in consumers to reduce their negative impact on humans. Inappropriate use of veterinary drugs in animal husbandry, such as tiamulin, leads to the appearance of residues in edible animal tissues. The use of natural substances of plant origin, extracted from hemp ( L.), such as cannabidiol (CBD), is one of the solutions to minimize the negative effects of tiamulin. This study aimed to determine the effect of CBD on the cytotoxicity of tiamulin in humans. The cytotoxic activity of tiamulin and the effect of its mixtures with CBD were tested after 72 h exposure to three human cell lines: SH-SY5Y, HepG2 and HEK-293. Cytotoxic concentrations (IC) of the tested drug and in combination with CBD were assessed using five biochemical endpoints: mitochondrial and lysosomal activity, proliferation, cell membrane integrity and effects on DNA synthesis. Oxidative stress, cell death and cellular morphology were also assessed. The nature of the interaction between the veterinary drug and CBD was assessed using the combination index. The long-term effect of tiamulin inhibited lysosomal (SH-SY5SY) and mitochondrial (HepG2) activity and DNA synthesis (HEK-293). IC values for tiamulin ranged from 2.1 to >200 µg/mL (SH-SY5SY), 13.9 to 39.5 µg/mL (HepG2) and 8.5 to 76.9 µg/mL (HEK-293). IC values for the drug/CBD mixtures were higher. Reduced levels of oxidative stress, apoptosis and changes in cell morphology were demonstrated after exposure to the mixtures. Interactions between the veterinary drug and CBD showed a concentration-dependent nature of tiamulin in cell culture, ranging from antagonistic (low concentrations) to synergistic effects at high drug concentrations. The increased risk to human health associated with the presence of the veterinary drug in food products and the protective nature of CBD use underline the importance of these studies in food toxicology and require further investigation.

摘要

人们对保护公众健康(包括食品安全)的意识日益增强且需求不断增加,这就需要深入研究兽药在消费者体内的作用机制,以减少其对人类的负面影响。在畜牧业中不当使用兽药,如泰妙菌素,会导致可食用动物组织中出现残留。使用从大麻(L.)中提取的植物源天然物质,如大麻二酚(CBD),是将泰妙菌素负面影响降至最低的解决方案之一。本研究旨在确定CBD对泰妙菌素在人体细胞毒性方面的影响。在将泰妙菌素及其与CBD的混合物暴露于三种人类细胞系(SH-SY5Y、HepG2和HEK-293)72小时后,测试了泰妙菌素的细胞毒性活性及其混合物的效果。使用五个生化终点评估受试药物及其与CBD组合的细胞毒性浓度(IC):线粒体和溶酶体活性、增殖、细胞膜完整性以及对DNA合成的影响。还评估了氧化应激、细胞死亡和细胞形态。使用组合指数评估兽药与CBD之间相互作用的性质。泰妙菌素的长期作用抑制了溶酶体(SH-SY5SY)和线粒体(HepG2)活性以及DNA合成(HEK-293)。泰妙菌素的IC值范围为2.1至>200μg/mL(SH-SY5SY)、13.9至39.5μg/mL(HepG2)和8.5至76.9μg/mL(HEK-293)。药物/CBD混合物的IC值更高。暴露于混合物后,氧化应激水平降低、细胞凋亡减少且细胞形态发生变化。兽药与CBD之间的相互作用在细胞培养中显示出泰妙菌素浓度依赖性的性质,范围从拮抗(低浓度)到高药物浓度时的协同作用。与食品中存在兽药相关的人类健康风险增加以及使用CBD的保护性质强调了这些研究在食品毒理学中的重要性,并需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85cb/11676896/88e5e143d19c/ijms-25-13542-g001.jpg

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