scholarly journals SECRETORY PROTEIN SYNTHESIS IN THE STIMULATED RAT PAROTID GLAND

1973 ◽  
Vol 59 (3) ◽  
pp. 708-721 ◽  
Author(s):  
John H. Lillie ◽  
Seong S. Han

Administration of the ß-adrenergic drug, isoproterenol (IPR), affects the release of 98% of stored amylase from rat parotid gland acinar cells. A period of 6 h elapses from the onset of secretion to the maximum [14C]phenylalanine (Phe) incorporation into total protein and amylase. 10 h after IPR administration the rate of [14C]Phe incorporation into total protein was no longer elevated above that of control. Incorporation into amylase, however, remained elevated above the control by 2.3 times. This latent period may reflect: (a) reduced amounts of available ATP which occurs as a result of the process of secretion as well as (b) the time required for reorganization of cellular organelles and membranes after secretion. The latent period after IPR-induced secretion appears similar to the latent period which has recently been reported to occur after physiologic release of amylase from the parotid gland during the diurnal feeding cycle of the rat. These observations support the existence of a positive feedback system operant in the parotid acinar cell linking the release of secretory proteins with their synthesis. The period of greatest protein synthesis is, however, temporally dissociated from the secretory process.

1971 ◽  
Vol 246 (12) ◽  
pp. 3879-3884 ◽  
Author(s):  
Leo M. Sreebny ◽  
Dorthea A. Johnson ◽  
Murray R. Robinovitch

1987 ◽  
pp. 195-196
Author(s):  
C. Dreux ◽  
V. Imhoff ◽  
P. Mauduit ◽  
B. Rossignol

1994 ◽  
Vol 28 (1) ◽  
pp. 34-44 ◽  
Author(s):  
Philippe Robin ◽  
Bernard Rossignol ◽  
Marie-No�lle Raymond

1998 ◽  
Vol 252 (3) ◽  
pp. 485-497 ◽  
Author(s):  
Savithri Sivakumar ◽  
Lily Mirels ◽  
Abigail J. Miranda ◽  
Arthur R. Hand

1978 ◽  
Vol 176 (1) ◽  
pp. 23-29 ◽  
Author(s):  
P Kanagasuntheram ◽  
S C Lim

1. Protein synthesis in the rat parotid gland in vitro was studied by measuring the incorporation of [3H]phenylalanine into trichloroacetic acid-insoluble proteins. In the unstimulated gland, the rate of incorporation was dependent on the phenylalanine concentration in the medium and proceeded linearly for up to 3h. 2. Adrenaline, carbamoylcholine, phenylephrine and ionophore A23187 inhibited the incorporation of [3H]phenylalanine into acid-insoluble protein; isoprenaline, dibutyryl cyclic AMP and 8-bromo-cyclic GMP were inactive. 3. Inhibition by adrenaline and carbamoylcholine but not by ionophore A23187 required extracellular Ca2+. 4. Both adrenaline and carbamoylcholine increased the magnitude of the acid-soluble [3H]phenylalanine pool at 10 micrometer extracellular phenylalanine, but had no effect if the phenylalanine concentration was increased to 200 micrometer. 5. There was no correlation between cellular ATP content and the observed inhibition of protein synthesis. 6. Our results suggest that both alpha-adrenergic and cholinergic receptors may play a role in the regulation of protein synthesis in the rat parotid gland, and that their effects are mediated by a rise in intracellular free Ca2+.


1980 ◽  
Vol 15 (2) ◽  
pp. 77-85 ◽  
Author(s):  
S.K. Kim ◽  
P.A. Weinhold ◽  
S.S. Han ◽  
D.J. Wagner

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