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地塞米松诱导的免疫抑制:兔模型

Dexamethasone-induced immunosuppression: a rabbit model.

作者信息

Jeklova Edita, Leva Lenka, Jaglic Zoran, Faldyna Martin

机构信息

Department of Immunology, Veterinary Research Institute, Hudcova 70, 621 00 Brno, Czech Republic.

出版信息

Vet Immunol Immunopathol. 2008 Apr 15;122(3-4):231-40. doi: 10.1016/j.vetimm.2007.11.011. Epub 2007 Dec 5.

Abstract

Rabbits are often used as animal models for experimental purposes; in many cases steroid-induced immunosuppression is necessary. The aim of this study was to characterise a model of immunosuppression in rabbits, based on changes in the lymphocyte subset distribution, changes in proliferative capacity of lymphocytes and activity of neutrophils 1, 3 and 7 days after the administration of 2mg/kg dexamethasone phosphate (DXP) three times at 6-h intervals. In peripheral blood, neutrophilia and lymphopenia together with eosinopenia, monocytopenia and basopenia in the absence of leukocytosis was detected. One day after DXP administration the absolute numbers of all lymphocyte subsets decreased in the blood, whereas in bone marrow, absolute numbers of all lymphocyte subsets increased significantly, except CD79alpha(+) cells that increased only in relative numbers. The effect of DXP on lymphocytes from the spleen, mesenteric and popliteal lymph nodes was less pronounced. In the thymus, DXP led to a marked reduction of the relative and absolute numbers of CD4(+)CD8(+) thymocytes. The proliferative capacity of lymphocytes after concanavalin A stimulation was lower in the peripheral blood and spleen only on day 1, no changes were detected in lymph nodes or in bone marrow. A marked increase in proliferative capacity was detected in the thymus. Spontaneous production of reactive oxygen metabolites by neutrophils was reduced on days 1 and 3 after DXP administration. The present results demonstrate clearly that this DXP application protocol is useful for the experimental induction of relatively short-lasting immunosuppression in rabbits.

摘要

兔子常被用作实验动物模型;在许多情况下,类固醇诱导的免疫抑制是必要的。本研究的目的是基于淋巴细胞亚群分布的变化、淋巴细胞增殖能力的变化以及在以6小时间隔三次给予2mg/kg地塞米松磷酸钠(DXP)后1天、3天和7天中性粒细胞的活性,来表征兔子的免疫抑制模型。在外周血中,检测到中性粒细胞增多和淋巴细胞减少,同时伴有嗜酸性粒细胞减少、单核细胞减少和嗜碱性粒细胞减少,且无白细胞增多。给予DXP后1天,血液中所有淋巴细胞亚群的绝对数量均减少,而在骨髓中,除CD79alpha(+)细胞仅相对数量增加外,所有淋巴细胞亚群的绝对数量均显著增加。DXP对脾脏、肠系膜淋巴结和腘淋巴结淋巴细胞的影响不太明显。在胸腺中,DXP导致CD4(+)CD8(+)胸腺细胞的相对和绝对数量显著减少。仅在第1天,外周血和脾脏中伴刀豆球蛋白A刺激后淋巴细胞的增殖能力较低,在淋巴结或骨髓中未检测到变化。在胸腺中检测到增殖能力显著增加。给予DXP后第1天和第3天,中性粒细胞活性氧代谢产物的自发产生减少。目前的结果清楚地表明,这种DXP应用方案对于在兔子中实验性诱导相对短暂的免疫抑制是有用的。

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