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慢性低氧对等容性高通气诱发的豚鼠支气管收缩的抑制作用。

Attenuation of isocapnic hyperpnoea-induced guinea-pig bronchoconstriction by chronic hypoxia.

作者信息

Lai Y L, Lin C W, Lai L C

机构信息

Dept of Physiology, National Taiwan University, College of Medicine, Taipei.

出版信息

Eur Respir J. 1998 May;11(5):1075-80. doi: 10.1183/09031936.98.11051075.

Abstract

Chronic hypoxia has been shown to augment the production of antioxidants in rat lungs and to reduce airway hyperreactivity in patients with asthma. This study investigated indirectly whether this increase in antioxidants occurs in guinea-pig lungs and whether the increased antioxidants affect hyperpnoea-induced bronchoconstriction (HIB). Guinea-pigs were divided into four groups: control (n=8); chronic hypoxia (n=7); capsaicin pretreatment (n=7); and capsaicin pretreatment plus chronic hypoxia (n=8). Control animals were not treated. Animals in the hypoxia group were intermittently exposed to an ambient pressure of 380 mmHg for 7 days. A five day pretreatment of capsaicin was used to deplete tachykinins. In the last group, animals were pretreated with capsaicin, followed by a seven day hypoxic exposure. On the day of the study, airway function was examined in the anaesthetized and paralysed animal. Fifteen minutes of hyperpnoea caused marked decreases in the maximal expiratory flow rate at 15% vital capacity, forced expiratory volume in one second, and dynamic respiratory compliance, indicating HIB. This HIB and plasma substance P levels were significantly attenuated by chronic hypoxia, capsaicin pretreatment, and capsaicin pretreatment plus chronic hypoxia. Furthermore, chronic hypoxia attenuated airway constriction induced by xanthine-xanthine oxidase. The results suggest that chronic hypoxia attenuates hyperpnoea-induced bronchoconstriction via a decrease in the oxygen radical-mediated release of tachykinins.

摘要

慢性缺氧已被证明可增加大鼠肺中抗氧化剂的产生,并降低哮喘患者的气道高反应性。本研究间接调查了豚鼠肺中是否会出现这种抗氧化剂增加的情况,以及增加的抗氧化剂是否会影响通气过度诱导的支气管收缩(HIB)。将豚鼠分为四组:对照组(n = 8);慢性缺氧组(n = 7);辣椒素预处理组(n = 7);辣椒素预处理加慢性缺氧组(n = 8)。对照组动物不进行处理。缺氧组动物间歇性暴露于380 mmHg的环境压力下7天。采用为期五天的辣椒素预处理来消耗速激肽。在最后一组中,动物先用辣椒素预处理,然后进行为期七天的缺氧暴露。在研究当天,对麻醉和麻痹的动物进行气道功能检查。通气过度15分钟导致15%肺活量时的最大呼气流量、一秒用力呼气量和动态呼吸顺应性显著降低,表明存在HIB。慢性缺氧、辣椒素预处理以及辣椒素预处理加慢性缺氧均显著减轻了这种HIB和血浆P物质水平。此外,慢性缺氧减轻了黄嘌呤 - 黄嘌呤氧化酶诱导的气道收缩。结果表明,慢性缺氧通过减少氧自由基介导的速激肽释放来减轻通气过度诱导的支气管收缩。

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