Buehler Philipp K, Bleiler Doris, Tegtmeier Ines, Heitzmann Dirk, Both Christian, Georgieff Michael, Lesage Florian, Warth Richard, Thomas Jörg
University Children's Hospital, Steinwiesstr. 75, CH-8032 Zürich, Switzerland.
Institute of Physiology, University of Regensburg, D-93053 Regensburg, Germany; Department of Anaesthesia, University Hospital Regensburg, 93042 Regensburg, Germany.
Respir Physiol Neurobiol. 2017 Oct;244:17-25. doi: 10.1016/j.resp.2017.06.009. Epub 2017 Jul 1.
Despite intensive research, the exact function of TASK potassium channels in central and peripheral chemoreception is still under debate. In this study, we investigated the respiration of unrestrained TASK-3 (TASK-3) and TASK-1/TASK-3 double knockout (TASK-1/3) adult male mice in vivo using a plethysmographic device. Ventilation parameters of TASK-3 mice were normal under control condition (21% O) and upon hypoxia and hypercapnia they displayed the physiological increase of ventilation. TASK-1/3 mice showed increased ventilation under control conditions. This increase of ventilation was caused by increased tidal volumes (V), a phenomenon similarly observed in TASK-1 mice. Under acute hypoxia, TASK-1/3 mice displayed the physiological increase of the minute volume. Interestingly, this increase was not related to an increase of the respiratory frequency (f), as observed in wild-type mice, but was caused by a strong increase of V. This particular respiratory phenotype is reminiscent of the respiratory phenotype of carotid body-denervated rodents in the compensated state. Acute hypercapnia (5% CO) stimulated ventilation in TASK-1/3 and wild-type mice to a similar extent; however, at higher CO concentrations (>5% CO) the stimulation of ventilation was more pronounced in TASK-1/3 mice. At hyperoxia (100% O), TASK-1, TASK-3 and wild-type mice showed the physiological small decrease of ventilation. In sharp contrast, TASK-1/3 mice exhibited an abnormal increase of ventilation under hyperoxia. In summary, these measurements showed a grossly normal respiration of TASK-3 mice and a respiratory phenotype of TASK-1/3 mice that was characterized by a markedly enhanced tidal volume, similar to the one observed in TASK-1 mice. The abnormal hyperoxia response, exclusively found in TASK-1/3 double mutant mice, indicates that both TASK-1 and TASK-3 are essential for the hyperoxia-induced hypoventilation. The peculiar respiratory phenotype of TASK-1/3 knockout mice is reminiscent of the respiration of animals with long-term carotid body dysfunction. Taken together, TASK-1 and TASK-3 appear to serve specific and distinct roles in the complex processes underlying chemoreception and respiratory control.
尽管进行了深入研究,但TASK钾通道在中枢和外周化学感受中的具体功能仍存在争议。在本研究中,我们使用体积描记装置在体内研究了无束缚的TASK-3(TASK-3)和TASK-1/TASK-3双敲除(TASK-1/3)成年雄性小鼠的呼吸情况。TASK-3小鼠在对照条件下(21%氧气)的通气参数正常,在缺氧和高碳酸血症时,它们的通气量出现生理性增加。TASK-1/3小鼠在对照条件下通气量增加。这种通气量的增加是由潮气量(V)增加引起的,这一现象在TASK-1小鼠中也有类似观察。在急性缺氧时,TASK-1/3小鼠的分钟通气量出现生理性增加。有趣的是,这种增加与野生型小鼠中观察到的呼吸频率(f)增加无关,而是由V的大幅增加引起的。这种特殊的呼吸表型让人联想到处于代偿状态的颈动脉体去神经啮齿动物的呼吸表型。急性高碳酸血症(5%二氧化碳)对TASK-1/3和野生型小鼠通气的刺激程度相似;然而,在更高的二氧化碳浓度(>5%二氧化碳)下,TASK-1/3小鼠的通气刺激更为明显。在高氧(100%氧气)条件下,TASK-1、TASK-3和野生型小鼠的通气量出现生理性小幅下降。与之形成鲜明对比的是,TASK-1/3小鼠在高氧条件下出现通气异常增加。总之,这些测量结果显示TASK-3小鼠的呼吸大致正常,而TASK-1/3小鼠的呼吸表型特征为潮气量明显增加,类似于在TASK-1小鼠中观察到的情况。仅在TASK-1/3双突变小鼠中发现的异常高氧反应表明,TASK-1和TASK-3对于高氧诱导的通气不足都是必不可少的。TASK-1/3基因敲除小鼠独特的呼吸表型让人联想到长期颈动脉体功能障碍动物的呼吸情况。综上所述,TASK-1和TASK-3似乎在化学感受和呼吸控制的复杂过程中发挥着特定且不同的作用。