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布洛芬不能逆转对慢性低氧的通气适应。

Ibuprofen does not reverse ventilatory acclimatization to chronic hypoxia.

作者信息

De La Zerda D J, Stokes J A, Do J, Go A, Fu Z, Powell F L

机构信息

Division of Pulmonary and Critical Care Medicinea, Department of Medicine, University of California, 9500 Gilman Drive La Jolla, Medicine San Diego, CA 92093, United States; Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Miami, 1600 NW 10th Ave RMSB, Suite 7063, Miami, FL 33136, United States.

Division of Physiology, Department of Medicine, University of California, 9500 Gilman Drive La Jolla, San Diego, CA 92093, United States.

出版信息

Respir Physiol Neurobiol. 2018 Oct;256:29-35. doi: 10.1016/j.resp.2017.07.009. Epub 2017 Jul 27.

Abstract

Ventilatory acclimatization to hypoxia involves an increase in the acute hypoxic ventilatory response that is blocked by non-steroidal anti-inflammatory drugs administered during sustained hypoxia. We tested the hypothesis that inflammatory signals are necessary to sustain ventilatory acclimatization to hypoxia once it is established. Adult, rats were acclimatized to normoxia or chronic hypoxia (CH, [Formula: see text] =70Torr) for 11-12days and treated with ibuprofen or saline for the last 2days of hypoxia. Ventilation, metabolic rate, and arterial blood gas responses to O and CO were not affected by ibuprofen after acclimatization had been established. Immunohistochemistry and image analysis showed acute (1h) hypoxia activated microglia in a medullary respiratory center (nucleus tractus solitarius, NTS) and this was blocked by ibuprofen administered from the beginning of hypoxic exposure. Microglia returned to the control state after 7days of CH and were not affected by ibuprofen administered for 2 more days of CH. In contrast, NTS astrocytes were activated by CH but not acute hypoxia and activation was not reversed by administering ibuprofen for the last 2days of CH. Hence, ibuprofen cannot reverse ventilatory acclimatization or astrocyte activation after they have been established by sustained hypoxia. The results are consistent with a model for microglia activation or other ibuprofen-sensitive processes being necessary for the induction but not maintenance of ventilatory acclimatization to hypoxia.

摘要

对低氧的通气适应包括急性低氧通气反应的增强,而在持续性低氧期间给予非甾体抗炎药可阻断这种增强。我们检验了这样一种假说,即一旦建立起对低氧的通气适应,炎症信号对于维持这种适应是必要的。成年大鼠在常氧或慢性低氧(CH,[公式:见正文]=70托)环境中适应11 - 12天,并在低氧的最后2天用布洛芬或生理盐水处理。在适应建立后,布洛芬对氧气和二氧化碳的通气、代谢率及动脉血气反应没有影响。免疫组织化学和图像分析显示,急性(1小时)低氧激活了延髓呼吸中枢(孤束核,NTS)中的小胶质细胞,而从低氧暴露开始给予布洛芬可阻断这种激活。在慢性低氧7天后,小胶质细胞恢复到对照状态,且在慢性低氧再持续2天期间给予布洛芬对其没有影响。相反,NTS星形胶质细胞被慢性低氧激活,但不被急性低氧激活,且在慢性低氧的最后2天给予布洛芬并不能逆转这种激活。因此,在持续性低氧建立起通气适应和星形胶质细胞激活后,布洛芬无法将其逆转。这些结果与一种模型相符,即小胶质细胞激活或其他对布洛芬敏感的过程对于诱导而非维持对低氧的通气适应是必要的。

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