Kir6.2 is required for adaptation to stress
Author(s) -
Leonid V. Zingman,
Denice M. Hodgson,
Peter Bast,
Garvan C. Kane,
Carmen Pérez-Terzic,
Richard J. Gumina,
Darko Pucar,
Martin Bienengraeber,
Petras P. Dzeja,
Takashi Miki,
Susumu Seino,
Alexey E. Alekseev,
André Terzic
Publication year - 2002
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.212315199
Subject(s) - adaptation (eye) , potassium channel , channelopathy , microbiology and biotechnology , stimulation , blockade , mediator , biophysics , ion channel , kir6.2 , chemistry , neuroscience , biology , protein subunit , biochemistry , receptor , gene
Reaction to stress requires feedback adaptation of cellular functions to secure a response without distress, but the molecular order of this process is only partially understood. Here, we report a previously unrecognized regulatory element in the general adaptation syndrome. Kir6.2, the ion-conducting subunit of the metabolically responsive ATP-sensitive potassium (K(ATP)) channel, was mandatory for optimal adaptation capacity under stress. Genetic deletion of Kir6.2 disrupted K(ATP) channel-dependent adjustment of membrane excitability and calcium handling, compromising the enhancement of cardiac performance driven by sympathetic stimulation, a key mediator of the adaptation response. In the absence of Kir6.2, vigorous sympathetic challenge caused arrhythmia and sudden death, preventable by calcium-channel blockade. Thus, this vital function identifies a physiological role for K(ATP) channels in the heart.
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