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The Journal of Neuroscience, August 27, 2008, 28(35):8844-8850; doi:10.1523/JNEUROSCI.1810-08.2008

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Behavioral/Systems/Cognitive
A Role for TASK-1 (KCNK3) Channels in the Chemosensory Control of Breathing

Stefan Trapp,1,2 M. Isabel Aller,3 William Wisden,4 and Alexander V. Gourine5

1Department of Anaesthetics, Pain Medicine and Intensive Care, Chelsea and Westminster Hospital, Imperial College London, London SW10 9NH, United Kingdom, 2Biophysics Section, Blackett Laboratory, Imperial College London, London SW7 2AZ, United Kingdom, 3Instituto de Neurociencias de Alicante, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández de Elche, Campus de San Juan, Apartado 18, Sant Joan d'Alacant, Spain, 4Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, United Kingdom, and 5Department of Physiology, University College London, London WC1E 6BT, United Kingdom

Correspondence should be addressed to Alexander V. Gourine, Department of Physiology, University College London, Gower Street, London WC1E 6BT, UK. Email: a.gourine{at}ucl.ac.uk

Acid-sensitive K+ channels of the tandem P-domain K+-channel family (TASK-1 and TASK-3) have been implicated in peripheral and central respiratory chemosensitivity; however, because of the lack of decisive pharmacological agents, the final proof of the role of the TASK channel in the chemosensory control of breathing has been missing. In the mouse, TASK-1 and TASK-3 channels are dispensable for central respiratory chemosensitivity (Mulkey et al., 2007). Here, we have used knock-out animals to determine whether TASK-1 and TASK-3 channels play a role in the carotid body function and chemosensory control of breathing exerted by the carotid body chemoreceptors. Ventilatory responses to hypoxia (10% O2 in inspired air) and moderate normoxic hypercapnia (3–6% CO2 in inspired air) were significantly reduced in TASK-1 knock-out mice. In contrast, TASK-3-deficient mice showed responses to both stimuli that were similar to those developed by their wild-type counterparts. TASK-1 channel deficiency resulted in a marked reduction of the hypoxia (by 49%)- and CO2 (by 68%)-evoked increases in the carotid sinus nerve chemoafferent discharge recorded in the in vitro superfused carotid body/carotid sinus nerve preparations. Deficiency in both TASK-1 and TASK-3 channels increased baseline chemoafferent activity but did not cause a further reduction of the carotid body chemosensory responses. These observations provide direct evidence that TASK-1 channels contribute significantly to the increases in the carotid body chemoafferent discharge in response to a decrease in arterial PO2 or an increase in PCO2/[H+]. TASK-1 channels therefore play a key role in the control of ventilation by peripheral chemoreceptors.

Key words: carotid body; chemosensitivity; hypercapnia; hypoxia; respiration; TASK


Received Dec. 24, 2007; revised July 16, 2008; accepted July 29, 2008.

Correspondence should be addressed to Alexander V. Gourine, Department of Physiology, University College London, Gower Street, London WC1E 6BT, UK. Email: a.gourine{at}ucl.ac.uk




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