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Histopathological outcome of Leishmania major-infected BALB/c mice is improved by oral treatment with N-acetyl-l-cysteine

机译:利什曼原虫主要感染BALB / c小鼠的组织病理学结果通过口服N-乙酰基-1-半胱氨酸治疗得到改善

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摘要

Leishmania major infected BALB/c mice were treated with N-acetyl-l-cysteine (NAC), a glutathione precursor, to evaluate the role of in vivo glutathione on lesion pathology and cytokine profiles following infection. Mice were maintained on NAC-containing water 2 days before infection for a total of 14 weeks. The BALB/c response to L. major infection was improved by oral administration of NAC, at the level of histopathological outcome, lesion progression and cytokine profile. A significantly improved histopathological outcome of the footpad lesion, characterized by a mixed inflammatory infiltrate organized in a focal pattern with little tissue destruction and a reduced parasite load, was observed in NAC-treated BALB/c mice. Histopathological modulation was accompanied by a modified cytokine pattern from popliteal lymph node cells, demonstrated by a sustained higher frequency of interferon-γ (IFN-γ) and tumour necrosis factor-α (TNF-α)-producing cells. This work points to an important role for glutathione in the modulation of effector responses in BALB/c mice.
机译:用N-乙酰基-1-半胱氨酸(NAC)(一种谷胱甘肽前体)处理了感染了利什曼原虫的严重BALB / c小鼠,以评估体内谷胱甘肽对感染后病变病理学和细胞因子谱的作用。在感染前2天,将小鼠保持在含NAC的水中,共14周。在组织病理学结果,病变进展和细胞因子水平,口服NAC可改善对大肠埃希氏菌的BALB / c反应。在NAC治疗的BALB / c小鼠中观察到足垫病变的组织病理学结果显着改善,其特征是混合的炎性浸润物以病灶模式组织,几乎没有组织破坏,并且寄生虫负荷降低。组织病理学调节伴随着来自pop淋巴结细胞的细胞因子模式的改变,其表现为持续较高的干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)产生细胞的频率。这项工作指出了谷胱甘肽在调节BALB / c小鼠效应反应中的重要作用。

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