4.7 Article

Sanguinarine induces apoptosis in Eimeria tenella sporozoites via the generation of reactive oxygen species

期刊

POULTRY SCIENCE
卷 101, 期 5, 页码 -

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ELSEVIER
DOI: 10.1016/j.psj.2022.101771

关键词

sanguinarine; Eimeria tenella; sporozoite; apoptosis

资金

  1. National Natural Science Foundation of China [32072888, 31941018, U21A20261]
  2. Science and Technology Development Program of Jilin Province [20180201040NY, 20190 301042NY, YDZJ202102CXJD029]

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This study found that sanguinarine can inhibit the invasion ability of Eimeria tenella sporozoites by increasing reactive oxygen species and calcium ions and decreasing mitochondrial membrane potential. It suggests that sanguinarine may be a potential therapeutic drug for coccidiosis.
Eimeria tenella (E. tenella) is the most pathogenic genus in Eimeria and can lead to a huge number of deaths of chickens, causing significant economic losses in the poultry industry worldwide. As a natural alkaloid, sanguinarine has many medicinal effects; to a certain extent, it can replace antibiotics and has good application prospects in veterinary medicine. To evaluate the effect of sanguinarine on sporozoites of E.tenella, we used flow cytometry and immunofluorescence staining to detect reactive oxygen species (ROS), mitochondrial membrane potential (MMP), calcium ion (Ca2+), and caspase-3 activation in E.tenella sporozoites treated with different concentrations of sanguinarine. The results of flow cytometry showed that sanguinarine could inhibit the invasion of sporozoites of E.tenella in vitro (P < 0.05) and increase the reactive oxygen species and calcium ions in the sporozoites (P < 0.05). The results of immunofluorescence staining showed that sanguinarine could decrease the mitochondrial membrane potential of sporozoites. Our analysis suggests that sanguinarine can induce apoptosis of E. tenella sporozoites through reactive oxygen species-mediated reduction of the mitochondrial membrane potential and an increase in calcium ion concentration. It follows that sanguinarine is likely to be a novel type of anticoccidiosis drug with good research and clinical application prospects.

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