scholarly journals Protein kinase C: subcellular redistribution by increased Ca2+ influx. Evidence that Ca2+-dependent subcellular redistribution of protein kinase C is involved in potentiation of beta-adrenergic stimulation of pineal cAMP and cGMP by K+ and A23187.

1988 ◽  
Vol 263 (19) ◽  
pp. 9292-9297
Author(s):  
A K Ho ◽  
T P Thomas ◽  
C L Chik ◽  
W B Anderson ◽  
D C Klein
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Adrenergic Stimulation ◽  
Beta Adrenergic ◽  
Kinase C ◽  
Camp And Cgmp ◽  
Stimulation Of

scholarly journals Stimulation of phosphoinositide metabolism in hamster brown adipocytes exposed to α1-adrenergic agents and its inhibition with phorbol esters

1986 ◽  
Vol 236 (3) ◽  
pp. 757-764 ◽  
Author(s):  
R J Schimmel ◽  
D Dzierzanowski ◽  
M E Elliott ◽  
T W Honeyman
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Time Course ◽  
Early Event ◽  
Phosphoinositide Metabolism ◽  
Adrenergic Stimulation ◽  
Brown Adipocytes ◽  
Adrenergic Agents ◽  
Kinase C ◽  
Stimulation Of

The present experiments were undertaken to investigate the role of the phosphoinositides phosphatidylinositol 4-phosphate (PtdIns-4-P) and phosphatidylinositol 4,5-biphosphate (PtdIns-4,5-P2) in the alpha 1-adrenergic stimulation of respiration in isolated hamster brown adipocytes. Exposure of isolated brown adipocytes to the alpha-adrenergic-receptor agonist phenylephrine provoked a breakdown of 30-50% of the PtdIns-4-P and PtdIns-4,5-P2 after prelabelling of the cells with [32P]Pi. Coincident with the breakdown of phosphoinositides was an accumulation of labelled phosphatidic acid, which continued for the duration of the cell incubation. The time course of phosphoinositide breakdown was defined more precisely by pulse-chase experiments. Under these conditions, phenylephrine caused radioactivity in phosphatidylinositol, PtdIns-4-P and PtdIns-4,5-P2 to fall by more than 50% within 30 s and to remain at the depressed value for the duration of the incubation (10 min). This phospholipid response to alpha-adrenergic stimulation was blocked by exposure of the cells to phorbol 12-myristate 13-acetate (PMA); likewise phenylephrine stimulation of respiration was prevented by PMA. beta-Adrenergic stimulation of respiration and inhibition of respiration by 2-chloroadenosine and insulin were, however, unaffected by treatment with PMA. On the assumption that PMA is acting in these cells as an activator of protein kinase C, these results suggest the selective interruption of alpha-adrenergic actions in brown adipocytes by activated protein kinase C. These findings suggest that breakdown of phosphoinositides is an early event in alpha-adrenergic stimulation of brown adipocytes which may be important for the subsequent stimulation of respiration. The results from the pulse-chase studies also suggest, however, that phenylephrine-stimulated breakdown of inositol phospholipids is a short-lived event which does not appear to persist for the entire period of exposure to the alpha 1-adrenergic ligand.

Alpha 1-adrenergic stimulation of Na-H exchange in cardiac myocytes

1992 ◽  
Vol 263 (5) ◽  
pp. C1096-C1102 ◽  
Author(s):  
M. A. Wallert ◽  
O. Frohlich
Keyword(s):  
Protein Kinase C ◽  
Steady State ◽  
Protein Kinase ◽  
Intracellular Ph ◽  
Ph Dependence ◽  
Adrenergic Stimulation ◽  
Adult Rat ◽  
Kinase C ◽  
Rat Heart Myocytes ◽  
Stimulation Of

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.

Altered pineal adrenergic-stimulated cyclic nucleotide responses in spontaneously hypertensive rats

1993 ◽  
Vol 264 (1) ◽  
pp. H157-H162
Author(s):  
C. L. Chik ◽  
A. K. Ho
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Cyclic Nucleotide ◽  
Spontaneously Hypertensive Rats ◽  
Similar Degree ◽  
Hypertensive Rats ◽  
Beta Adrenergic ◽  
Spontaneously Hypertensive ◽  
Kinase C ◽  
Camp And Cgmp

In this study, we examined the pineal adrenergic-stimulated cyclic nucleotide responses in spontaneously hypertensive rats (SHR) and their genetic control, Wistar-Kyoto rats (WKY). Treatment with norepinephrine stimulated cAMP and cGMP contents up to 50- and 12-fold in WKY pinealocytes, compared with a 35- and 4-fold increase in SHR. By contrast, there was no difference in the isoproterenol-stimulated cAMP and cGMP contents, suggesting a reduced alpha 1-adrenergic potentiation of beta-adrenergic-stimulated cGMP response in SHR pinealocytes. The altered potentiation mechanism was examined using agents that activate protein kinase C or elevate intracellular Ca2+. In the presence of a protein kinase C activator, the isoproterenol-stimulated cAMP response was potentiated to a similar degree in WKY and SHR pinealocytes. In contrast, the potentiating effects of ionomycin and KCl on the isoproterenol-stimulated cAMP and cGMP responses in SHR pinealocytes were markedly reduced. These results indicate that in the SHR pineal gland, an altered intracellular Ca(2+)-mediated event may account for the reduction in alpha 1-adrenergic potentiation of beta-adrenergic-stimulated cyclic nucleotide responses.

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