首页> 外文期刊>Polish journal of veterinary sciences >Evaluation of the influence of meloxicam and flunixin meglumine on the apoptosis of peripheral blood CD4+ and CD8+ T cells in calves.
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Evaluation of the influence of meloxicam and flunixin meglumine on the apoptosis of peripheral blood CD4+ and CD8+ T cells in calves.

机译:评价美洛昔康和氟尼辛葡甲胺对犊牛外周血CD4 + 和CD8 + T细胞凋亡的影响。

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摘要

The aim of the study was to determine whether treatment with recommended doses of meloxicam or flunixin had an effect on the apoptosis of peripheral blood T lymphocytes in calves. The study was carried out on 4-5 months old calves (n=24, 8 per group). Experimental animals were injected subcutaneously with a single dose of 0.5 mg.kg-1 of meloxicam or intravenously with 3 doses of 2.2 mg.kg-1 day-1 of flunixin. The non-treatment animals served as control. Blood samples were taken at day 0 and at days 1, 2, 3, 5, 7 and 14 after the first NSAIDs injection. Apoptosis was determined by flow cytometry using Annexin V-PE/7-AAD staining. The kinetic analysis of apoptosis in the total lymphocyte population, as well as in the CD4+ and CD8+ subsets did not reveal significant differences in the frequency of early apoptotic cells between control and experimental groups throughout the period studied. Although, 24 h after administration of the first dose of NSAIDs, late-stage apoptosisecrosis was significantly increased in the total lymphocyte population (the meloxicam group), as well as in the CD4+ (the meloxicam group and the flunixin group) and CD8+ (the flunixin group) subsets of T cells. However, this disturbance was transient, relatively poorly expressed and, thus, unlikely to be of clinical significance. Our results indicate that the use of meloxicam or flunixin in accordance with the recommended dosage regimen in cattle do not have a clinically significant influence on apoptosis of peripheral blood T cells.
机译:该研究的目的是确定用推荐剂量的美洛昔康或氟尼辛治疗是否对小牛外周血T淋巴细胞的凋亡有影响。该研究是在4-5个月大的犊牛上进行的(n = 24,每组8只)。给实验动物皮下注射0.5 mg.kg -1 的美洛昔康或静脉内注射3剂2.2 mg.kg -1 day -1 氟尼辛。非治疗动物用作对照。首次注射NSAID后第0天和第1、2、3、5、7和14天采集血样。使用膜联蛋白V-PE / 7-AAD染色通过流式细胞术确定凋亡。在总淋巴细胞群以及CD4 + 和CD8 + 亚群中凋亡的动力学分析没有显示对照组之间早期凋亡细胞频率的显着差异和整个研究期间的实验组。尽管在首次服用NSAIDs后24小时,总淋巴细胞群体(美洛昔康组)以及CD4 + (美洛昔康)的晚期凋亡/坏死明显增加组和氟尼辛组)和CD8 + (氟尼辛组)T细胞亚群。但是,这种干扰是短暂的,表达相对较差,因此不太可能具有临床意义。我们的结果表明,按照推荐的剂量方案在牛中使用美洛昔康或氟尼辛对外周血T细胞的凋亡没有临床显着影响。

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