Alpha 1-adrenergic stimulation and phorbol ester shifted the intracellular pH dependence of Na-H exchange by 0.10-0.15 pH units in the alkaline direction in adult rat heart myocytes.
Adrenergic stimulation of cardiac Na-H exchange is mediated by an alpha 1-adrenergic mechanism that likely involves the activation of protein kinase C.
Effect estimate: 0.10-0.15 pH units shift
The activation of Na-H exchange in adult rat heart myocytes was characterized in response to a phorbol ester (phorbol 12-myristate 13-acetate) and an alpha 1-adrenergic agonist 6-fluoronorepinephrine (6F-NE). Transport activation was assessed by determining the initial rate with which intracellular pH (pHi) was returned from an acid pulse and by following changes in steady-state pHi; pHi was determined by a pH-sensitive fluorescent dye. Both agonists shifted the intracellular pH dependence of Na-H exchange by 0.10-0.15 pH units in the alkaline direction. This shift was prevented by the presence of sphingosine and 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine (H-7), inhibitors of protein kinase C. The agonists also alkalinized pHi at steady state. The alkalinization by 6F-NE was blocked by prazosin and H-7. This indicates that the adrenergic stimulation of cardiac Na-H exchange is mediated by an alpha 1-adrenergic mechanism and very likely involves the activation of protein kinase C.
Wallert et al. (Sun,) reported a other. Phorbol ester and alpha 1-adrenergic agonist (6-fluoronorepinephrine) was evaluated on Intracellular pH dependence of Na-H exchange (0.10-0.15 pH units shift). Alpha 1-adrenergic stimulation and phorbol ester shifted the intracellular pH dependence of Na-H exchange by 0.10-0.15 pH units in the alkaline direction in adult rat heart myocytes.