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正、负加速度交替急性大鼠脑组织NO、NOS及血浆ET的含量变化 被引量:2

Variation of NO,NOS level of brain tissue and plasma ET in rats induced by positive and negative acceleration
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摘要 目的 :研究正、负加速度交替暴露后急性大鼠脑组织一氧化氮 (NO)、一氧化氮合酶 (NOS)及血浆内皮素 (ET)的含量变化 ,探讨正、负加速度交替暴露后 ,易发生加速度引起意识丧失 (G -inducedlessofconsciousness ,G -LOC)的机制。方法 :30只雄性Wistar大鼠随机分成 3组 :对照组、正加速度 ( +Gz)组和正、负加速度 ( +Gz和 -Gz)交替组。于暴露后即刻麻醉采血、取脑 ,测定脑组织NO、NOS及血浆中ET的含量。结果 :+Gz组和 +Gz、-Gz交替组与对照组比较 ,脑组织中的NO、NOS及血浆中ET的含量增多 ,有显著性差异 ;+Gz、-Gz交替组与 +Gz组比较 ,脑组织中的NO、NOS及血浆中ET的含量增多 ,有差异性。结论 :+Gz、-Gz交替暴露和单纯 +Gz暴露均可使脑组织中的NO、NOS及血浆中ET的含量增多 ;且 +Gz、-Gz交替暴露增多明显。说明 +Gz。 Objective:To investigate the changes of nitric oxide (NO) and nitric oxide synthase(NOS) level of brain tissue and blood plasma endothelin (ET) in Wistar rats immediately after positive and negative acceleration, and explore the mechanism of G-induced less of consciousness(G-LOC). Methods:Thirty rats were divided into 3 groups at random:control group,+Gz group and +Gz --Gz group. The control group was under +1 Gz loads. The +Gz group was under +5 Gz loads and maintained for 40 seconds, then turned to +10 Gz loads for 2 minutes. The +Gz-Gz group was first under +5 Gz loads for 30 seconds, then turned to -5 Gz loads for 5 seconds, and returned to +5 Gz at once, the loads was increased to +10 Gz and lasted for 2 minutes. The growth rate was 1G/s. Repeated for 4 times, the interval was about 5 minutes. Rats were anesthetized immediately to collect blood and brain tissue in order to detect the content of NO, NOS of brain tissue and ET of the plasma. Results:The content of NO,NOS and ET of +Gz group and +Gz--Gz group were increased significantly in comparison with the control, and they were significantly higher in +Gz--Gz group than that in +Gz group. Conclusion: +Gz and +Gz--Gz lead to increase of NO, NOS and ET. +Gz after -Gz repeatedly is more harmful to brain.
出处 《西北国防医学杂志》 CAS 2003年第5期325-327,共3页 Medical Journal of National Defending Forces in Northwest China
基金 全军"十五"医药卫生科研基金项目 (0 1MA2 0 2 )
关键词 加速度 一氧化氮 一氧化氮合酶 内皮素 Acceleration Nitric oxide Nitric oxide synthase Endothelin
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