Catecholamines and divalent cations restored propagated action potentials to guinea pig atrial muscle fibers depolarized by elevated potassium, likely by increasing membrane conductance to calcium.
Depolarized atrial muscle fibers
Catecholamines (isoproterenol, epinephrine, norepinephrine) and divalent cations
Restoration of propagated action potentials and contractions
Atrial muscle fibers of the guinea pig were depolarized and rendered inexcitable by elevation of K + o to 22 m M . Isoproterenol, epinephrine, and norepinephrine restored propagated action potentials and contractions to atrial cells without changing the resting potential. The peak value of the intracellularly recorded action potentials varied 28 mv for a 10-fold change in Ca 2+ o . Isoproterenol-induced restoration of action potentials was insensitive to large concentrations of tetrodotoxin (3 x 10 -6 M ) but antagonized by Mn 2+ (0.2 m M ). These data supported the proposal that the catecholamines restored excitability by increasing membrane conductance to Ca 2+ . In addition to the catecholamines, the divalent cations Ba 2+ , Sr 2+ , and Ca 2+ restored action potentials to atrial muscle fibers depolarized by elevated K + . The effectiveness of the divalent ions in allowing action potentials was inversely related to the estimated hydrated ionic radii. Like the action potentials observed in the presence of isoproterenol, those permitted by Ba 2+ , Sr 2+ , and Ca 2+ were prevented by Mn 2+ but insensitive to blockade by tetrodotoxin.
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Achilles J. Pappano
University of Connecticut
Circulation Research
UConn Health
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Achilles J. Pappano (Tue,) conducted a other in Depolarized atrial muscle fibers. Catecholamines (isoproterenol, epinephrine, norepinephrine) and divalent cations was evaluated on Restoration of propagated action potentials and contractions. Catecholamines and divalent cations restored propagated action potentials to guinea pig atrial muscle fibers depolarized by elevated potassium, likely by increasing membrane conductance to calcium.
synapsesocial.com/papers/6a0fb2332badbc352afe8fb8 — DOI: https://doi.org/10.1161/01.res.27.3.379