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奥美拉唑对小鼠微小隐孢子虫抗寄生虫作用的体内研究

In Vivo Study on the Anti-Parasitic Effect of Omeprazole on Cryptosporidium parvum in Mice.

作者信息

Atallah Mai A, El-Kowrany Samy I, Afifi Omayma K, Elkaliny Heba H, Younis Salwa S, Gamea Ghada A

机构信息

Medical Parasitology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

Histology and Cell Biology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

出版信息

Parasite Immunol. 2025 Jun;47(6):e70012. doi: 10.1111/pim.70012.

Abstract

Cryptosporidiosis is an important enteric disease, causing diarrhoea and malabsorption similar to Rotavirus and targeting young children and immunocompromised individuals, especially AIDS patients. However, there is a lack of fully effective drugs and vaccines against it. This study was done with the aim of investigating the anti-parasitic and anti-inflammatory effects of omeprazole versus nitazoxanide and their combination on Cryptosporidium parvum (C. parvum) infection in immunosuppressed experimental mice. To achieve this aim, histopathological analysis, scanning electron microscopy (SEM), estimation of oocyst shedding and measurement of tumour necrosis factor alpha (TNF-α) levels in sera of mice and the optical density of inducible nitric oxide synthase (iNOS) immunoreactivity in intestinal tissues were performed. Regarding the results, oocyst shedding showed an obvious reduction with omeprazole more than nitazoxanide. Similar results were detected on both histopathological examination (by haematoxylin and eosin and periodic acid-Schiff stains) and SEM with marked improvement in pathology detected in the combination therapy treated group. TNF-α showed reduced levels in the sera of all treated groups indicating a reduction of immunopathology with treatment. Also, the cytoplasmic expression of iNOS in the intestinal epithelium of mice was markedly reduced in all treated groups indicating a reduction of oxidative stress. From these results, omeprazole was found to be superior to nitazoxanide in treating cryptosporidiosis and the use of the two drugs as a combined therapy showed the best results.

摘要

隐孢子虫病是一种重要的肠道疾病,可引起与轮状病毒相似的腹泻和吸收不良,主要影响幼儿和免疫功能低下的个体,尤其是艾滋病患者。然而,目前缺乏针对该病的完全有效的药物和疫苗。本研究旨在调查奥美拉唑与硝唑尼特及其联合用药对免疫抑制实验小鼠微小隐孢子虫(C. parvum)感染的抗寄生虫和抗炎作用。为实现这一目标,进行了组织病理学分析、扫描电子显微镜(SEM)检查、卵囊排出量估计、小鼠血清中肿瘤坏死因子α(TNF-α)水平测定以及肠道组织中诱导型一氧化氮合酶(iNOS)免疫反应性的光密度测量。结果显示,与硝唑尼特相比,奥美拉唑使卵囊排出量明显减少。在组织病理学检查(苏木精和伊红染色以及过碘酸-希夫染色)和SEM检查中均检测到类似结果,联合治疗组的病理学有明显改善。所有治疗组小鼠血清中的TNF-α水平均降低,表明治疗可减轻免疫病理学变化。此外,所有治疗组小鼠肠道上皮细胞中iNOS的细胞质表达均明显降低,表明氧化应激减轻。从这些结果可以看出,在治疗隐孢子虫病方面,奥美拉唑优于硝唑尼特,两种药物联合使用效果最佳。

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