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红霉素、氟尼辛葡甲胺、左旋咪唑与植物次生代谢产物对牛胃肠动力的相互作用——体外研究

Interactions between erythromycin, flunixin meglumine, levamisole and plant secondary metabolites towards bovine gastrointestinal motility-in vitro study.

作者信息

Mendel M, Chłopecka M, Dziekan N, Karlik W

机构信息

Division of Pharmacology and Toxicology, Department of Preclinical Sciences, Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Warsaw, Poland.

出版信息

J Vet Pharmacol Ther. 2018 Apr;41(2):281-291. doi: 10.1111/jvp.12455. Epub 2017 Sep 14.

Abstract

Continued ingestion of plant secondary metabolites by ruminants can provoke pharmacological interactions with pharmaceutical agents used in animals. As some drugs and phytocompounds affect smooth muscle activity, the aim of this study was to verify the possible interaction between selected pharmaceutical agents and plant secondary metabolites towards bovine gastrointestinal motility. The interactions between phytocompounds-apigenin, quercetin, hederagenin, medicagenic acid-and medicines-erythromycin, flunixin meglumine and levamisole-were evaluated on bovine isolated abomasal and duodenal specimens obtained from routinely slaughtered cows. The obtained results confirmed the contractile effect of all three drugs used solely. Hederagenin and medicagenic acid (0.001 μM) enhanced the contractile effect of levamisole. Hederagenin additionally increased the impact of erythromycin. Both saponins (100 μM) showed synergistic effects with all tested pharmaceuticals. Apigenin and quercetin (0.001 μM) intensified the contractile response induced by erythromycin and levamisole. Moreover, both flavonoids (100 μM) showed an antagonistic interaction with all tested drugs which in that situation were devoid of the prokinetic effect. To conclude, plant metabolic metabolites such as saponins and flavonoids are potent modifiers of the effect of drugs towards gut motility. The synergy observed between phytocompounds and selected medicines can be beneficial in the treatment of cows with hypomotility disorders.

摘要

反刍动物持续摄入植物次生代谢产物可能会引发与动物所用药物的药理相互作用。由于一些药物和植物化合物会影响平滑肌活动,本研究的目的是验证所选药物与植物次生代谢产物对牛胃肠动力的可能相互作用。在从常规屠宰的奶牛获得的牛离体皱胃和十二指肠标本上,评估了植物化合物(芹菜素、槲皮素、常春藤皂苷元、地锦酸)与药物(红霉素、氟尼辛葡甲胺和左旋咪唑)之间的相互作用。所得结果证实了单独使用的所有三种药物的收缩作用。常春藤皂苷元和地锦酸(0.001 μM)增强了左旋咪唑的收缩作用。常春藤皂苷元还增加了红霉素的作用效果。两种皂苷(100 μM)与所有测试药物均显示出协同作用。芹菜素和槲皮素(0.001 μM)增强了红霉素和左旋咪唑诱导的收缩反应。此外,两种黄酮类化合物(100 μM)与所有测试药物均显示出拮抗相互作用,在这种情况下,这些药物没有促动力作用。总之,植物代谢产物如皂苷和黄酮类化合物是药物对肠道动力作用的有效调节剂。植物化合物与所选药物之间观察到的协同作用可能有利于治疗患有胃肠动力障碍的奶牛。

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