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作 者:王芳芳[1] 方以群[1] 攸璞[1] 包晓辰[1] 马骏[1] 张师[1]
机构地区:[1]海军医学研究所,上海200433
出 处:《中国应用生理学杂志》2015年第5期401-404,共4页Chinese Journal of Applied Physiology
基 金:海军后勤部科研基金项目(12A106);总后十二五重点科研课题(BWS11J053;BHJ12J003)
摘 要:目的:研究不同压力氧气对大鼠减压病的预防作用。方法:40只雄性SD大鼠,随机分为减压病组、1 ATA预吸氧组、2 ATA预吸氧组、3 ATA预吸氧组。减压病组置于脱险舱内,以"压缩空气3 min内匀速加压至0.7 MPa,停留60 min后,3 min内匀速减压"方案处理后出舱。预吸氧组分别于进舱前吸不同压力的氧20 min后再按上述方案加减压出舱。出舱后30 min内观测大鼠死亡率、行为学改变;取大鼠肺组织,测其干湿重比、支气管肺泡灌洗液蛋白量以及肿瘤坏死因子(TNF-α)表达含量变化。结果:和减压病组比较,预吸氧对减压病的死亡率及发病率无明显影响。但1 ATA预吸氧组大鼠支气管肺泡灌洗液蛋白量和炎症因子TNF-α值下降明显,肺干湿重比升高明显(P<0.05)。结论:预吸氧对减压病的死亡率及发病率无明显改善,但是常压吸氧可减轻存活大鼠肺泡灌洗液中蛋白渗透、降低肺组织中炎症因子的表达。Objective: To investigate the effect of different pressure oxygen pre-breathing in preventing decompression sickness of rats. Methods: Forty male SD rats were randomly divided into 4 groups: decompression sickness (DCS) group and three oxygen pre-breathing groups with 1 ATA, 2 ATA and 3 ATA pressure respectively. The rats of DCS group were placed in the hyperbaric chamber and the chamber was compressed evenly within 3 minutes to depths of 7 absolute atmosphere(ATA) and held at the designated depth for 60 min, then decom- pressed (3 rain) at constant speed to the surface pressure. After that, the rats were taken out for further detection. While the rats of oxygen pretreatment groups pre-breathed different pressure oxygen for 20 min before entering into chamber. The mortality and behavioral of rats were observed with 30 min post decompression. The dry/wet ratio of the lung, protein levels in the brenchoalveolar lavage fluid (BALF), and the inflammatory cytokine tumor necrosis factor (TNF-a) expression were also tested. Results: Compared with that of the DCS group, the mortality and morbidity of oxygen pre-breathe groups didn' t change obviously. But the total BALF protein level and the inflammatory cytokine TNF-a ex- pression of 1 ATA oxygen pre-breathe group were obviously decreased, while the dry/wet ratio of lung as obviously increased instead( P 〈 0.05). Conclusion: Although preoxygenation can' t obviously change the mortality and mobidity of rats, normal pressure oxygen pre-breathing can mitigate the protein infiltration in BALF and the expression of inflammatory cytokine in lung tissue.
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