Mechanisms that match ATP supply to demand in cardiac pacemaker cells during high ATP demand

The spontaneous action potential (AP) firing rate of sinoatrial node cells (SANCs) involves high-throughput signaling via Ca(2+)-calmodulin activated adenylyl cyclases (AC), cAMP-mediated protein kinase A (PKA), and Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)-dependent phosphorylation of...

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Vydané v:American journal of physiology. Heart and circulatory physiology Ročník 304; číslo 11; s. H1428
Hlavní autori: Yaniv, Yael, Spurgeon, Harold A, Ziman, Bruce D, Lyashkov, Alexey E, Lakatta, Edward G
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 01.06.2013
Predmet:
Adenosine Triphosphate - metabolism
Animals
Biological Clocks - physiology
Calcium Signaling - physiology
Calcium-Calmodulin-Dependent Protein Kinase Type 2 - physiology
Cell Separation
Cyclic AMP - metabolism
Cyclic AMP-Dependent Protein Kinases - physiology
Cytosol - metabolism
Flavoproteins - metabolism
Heart - physiology
Heart Rate - physiology
In Vitro Techniques
Mitochondria, Heart - metabolism
Mitochondria, Heart - physiology
Myocardial Contraction - physiology
Myocardium - cytology
Myocardium - metabolism
Myocytes, Cardiac - metabolism
Myocytes, Cardiac - physiology
Oxygen Consumption - physiology
Phosphoprotein Phosphatases - antagonists & inhibitors
Rabbits
Receptors, Adrenergic, beta - physiology
Respiratory Rate - physiology
bioenergetics
pacemaker automaticity
calcium-activated adenylyl cyclase
ISSN:1522-1539, 1522-1539
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Shrnutí:The spontaneous action potential (AP) firing rate of sinoatrial node cells (SANCs) involves high-throughput signaling via Ca(2+)-calmodulin activated adenylyl cyclases (AC), cAMP-mediated protein kinase A (PKA), and Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)-dependent phosphorylation of SR Ca(2+) cycling and surface membrane ion channel proteins. When the throughput of this signaling increases, e.g., in response to β-adrenergic receptor activation, the resultant increase in spontaneous AP firing rate increases the demand for ATP. We hypothesized that an increase of ATP production to match the increased ATP demand is achieved via a direct effect of increased mitochondrial Ca(2+) (Ca(2+)m) and an indirect effect via enhanced Ca(2+)-cAMP/PKA-CaMKII signaling to mitochondria. To increase ATP demand, single isolated rabbit SANCs were superfused by physiological saline at 35 ± 0.5°C with isoproterenol, or by phosphodiesterase or protein phosphatase inhibition. We measured cytosolic and mitochondrial Ca(2+) and flavoprotein fluorescence in single SANC, and we measured cAMP, ATP, and O₂ consumption in SANC suspensions. Although the increase in spontaneous AP firing rate was accompanied by an increase in O₂ consumption, the ATP level and flavoprotein fluorescence remained constant, indicating that ATP production had increased. Both Ca(2+)m and cAMP increased concurrently with the increase in AP firing rate. When Ca(2+)m was reduced by Ru360, the increase in spontaneous AP firing rate in response to isoproterenol was reduced by 25%. Thus, both an increase in Ca(2+)m and an increase in Ca(2+) activated cAMP-PKA-CaMKII signaling regulate the increase in ATP supply to meet ATP demand above the basal level.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1522-1539
1522-1539
DOI:10.1152/ajpheart.00969.2012