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JBC, Vol. 252, Issue 11, 3629-3636, Jun, 1977
B. E. Miller and D. L. Nelson
Rat parotid acinar cells dispersed by a combination of enzymatic treatments
remain sensitive to adrenergic and cholinergic agonists. Previous studies
have implicated Ca2+ in both adrenergic and cholinergic responses. This
paper describes the effects of adrenergic and cholinergic stimulation upon
45Ca2+ fluxes in isolated parotid acinar cells. Suspensions of dispersed
cells took up 45Ca2+ from the medium. The net rate of isotope influx was
increased by the adrenergic agonists epinephrine, norepinephrine,
isoproterenol, and phenylephrine, and by the cholinergic agonists
acetylcholine and carbamylcholine. In 1 mM Ca2+, epinephrine was capable of
increasing the 45Ca2+ influx in 40 min to three times that of resting
cells. Isoproterenol, a beta-adrenergic agonist, was only half as effective
as epinephrine in stimulating maximal calcium uptake although it was
equally effective in stimulating maximal amylase release in the same cells.
Experiments with the alpha-adrenergic antagonist phentolamine, the
beta-adrenergic antagonist propranolol, and the cholinergic antagonist
atropine confirmed that alpha- and beta-adrenergic and cholinergic
stimulation each had a direct stimulatory effect on 45Ca2+ uptake.
N6,O2'-Dibutyryl adenosine 3':5'-monophosphate also caused some stimulation
of net calcium uptake. Direct measurement of Ca2+ efflux indicated that the
increased calcium uptake in the presence of epinephrine was not the
indirect result of a decrease in efflux. The rates of both basal and
epinephrine-stimulated calcium uptake increased with increasing calcium
concentration in the medium. Epinephrine had little effect on the rate of
calcium uptake at 0.15 mM Ca2+. Although the energy poison NaCN had little
effect on the basal rate of calcium uptake, the stimulable component of
calcium uptake was inhibited by NaCN at all calcium concentrations tested
(0.2 to 4.1 mM).
Calcium fluxes in isolated acinar cells from rat parotid. Effect of adrenergic and cholinergic stimulation
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