Shi Min, Cui Fang, Yang Chang-Ying, Zhang Hao, Wang Ying-Ping, Wei Lin, Zhou Zhao-Nian, Zhang Yi
Department of Clinical Laboratory, The Second Hospital, Shijiazhuang 050017, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2009 Nov;25(4):433-8.
To elucidate the effect of CIHH on cellular immunity and humoral immunity in rat by using flow cytometry method, immunohistochemistry method and electron microscopy techniques.
Forty-eight male adult Sprague-Dawley rats were randomly divided into 4 groups: control(CON) group, 14 days CIHH (CIHH14) group, 28 days CIHH (CIHH28) group, 42 days CIHH (CIHH42) group. The animals in CIHH groups were exposed to 14, 28 and 42 days hypobaric hypoxia(simulated 3 000 m altitude, 5 h per day), respectively. Half of the animals in each group was treated with normaxia and the other half animals were treated with acute hypoxia for 1 h. CD3, CD4, CD8 T lymphocytes, natural killer (NK) cells, IgG, cortisol, epirenamine and C-reactive protein were examined. The weight and ultrastructure of thymus and spleen were observed.
(1) Compared with CON, both indexes of thymus and spleen in CIHH14 rats were increased significantly. Spleen index, but not thymus index, was increased in CIHH28 and CIHH42 rats. The thymocytes and spleen cytes in rat were injuryed during acute hypoxia, but the damage in CIHH rats was significant slighter than that in CON rats. (2) Compared with CON, CIHH28 and CIHH42, CD8 in CIHH14 rats were decreased, ratios of CD4/CD8 was increased and NK was decreased. (3) The rats of CON during acute hypoxia showed that CD4 was increased, CD8 was decreased, ratio of CD4/CD8 was elevated, and NK was increased. But there were no significant changes of CD3, CD4, CD8 and NK in CIHH28 and CIHH42 animals during acute hypoxia. (4) Compared with CON, CIHH28 and CIHH42, cortisol in CIHH14 rats was increased obviously, Epirenamine, cortisol and C-reactive protein in CON rats were increased, but there were no obvious changes in CIHH rats before and after acute hypoxia.
CIHH protects the immune function of rat against acute hypoxia, which is related with the regulation of neuroendocrine.
采用流式细胞术、免疫组织化学方法及电子显微镜技术,阐明慢性间歇性低氧(CIHH)对大鼠细胞免疫和体液免疫的影响。
48只成年雄性Sprague-Dawley大鼠随机分为4组:对照组(CON)、CIHH 14天组(CIHH14)、CIHH 28天组(CIHH28)、CIHH 42天组(CIHH42)。CIHH组动物分别暴露于14、28和42天的低压低氧环境(模拟海拔3000米,每天5小时)。每组一半动物进行常氧处理,另一半动物进行1小时急性低氧处理。检测CD3、CD4、CD8 T淋巴细胞、自然杀伤(NK)细胞、IgG、皮质醇、肾上腺素和C反应蛋白。观察胸腺和脾脏的重量及超微结构。
(1)与CON组相比,CIHH14大鼠胸腺和脾脏的各项指标均显著增加。CIHH28和CIHH42大鼠脾脏指数增加,但胸腺指数未增加。大鼠胸腺细胞和脾细胞在急性低氧时受到损伤,但CIHH大鼠的损伤明显轻于CON大鼠。(2)与CON、CIHH28和CIHH42组相比,CIHH14大鼠CD8降低,CD4/CD8比值升高,NK降低。(3)CON组大鼠在急性低氧时CD4增加,CD8降低,CD4/CD8比值升高,NK增加。但CIHH28和CIHH42组动物在急性低氧时CD3、CD4、CD8和NK无明显变化。(4)与CON、CIHH28和CIHH42组相比,CIHH14大鼠皮质醇明显增加,CON组大鼠肾上腺素、皮质醇和C反应蛋白增加,但CIHH组大鼠在急性低氧前后无明显变化。
CIHH可保护大鼠免疫功能免受急性低氧影响,这与神经内分泌调节有关。