Abstract
1. Incubation of submaxillary-gland slices with isoproterenol, a beta-adrenergic agonist, stimulated glucose removal by 41% and decreased tissue [glucose 6-phosphate] by 50%. Propranolol blocked these effects of isoproterenol. 2. Phenylephrine, an alpha-adrenergic agonist, stimulated glucose removal by 35% and decreased tissue [glucose 6-phosphate] by 75%. In addition, phenylephrine also completely overcame the inhibition of pyruvate removal caused by acetoacetate metabolism and decreased tissue [atp] by 45%. Phentolamine blocked the effects of phenylephrine. 3. In contrast with beta-adrenergic stimulation, alpha-adrenergic stimulation required exogenous Ca2+. 4. These results explain the different metabolic responses of the submaxillary gland to adrenaline in the presence and absence of exogenous Ca2+.
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Selected References
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- Batzri S., Selinger Z. Enzyme secretion mediated by the epinephrine -receptor in rat parotid slices. Factors governing efficiency of the process. J Biol Chem. 1973 Jan 10;248(1):356–360. [PubMed] [Google Scholar]
- Batzri S., Selinger Z., Schramm M., Robinovitch M. R. Potassium release mediated by the epinephrine -receptor in rat parotid slices. Properties and relation to enzyme secretion. J Biol Chem. 1973 Jan 10;248(1):361–368. [PubMed] [Google Scholar]
- Herman G., Rossignol B. Regulation of protein secretion and metabolism in rat salivary glands. Effects of norepinephrine and carbachol on the glycogenolysis in submaxillary glands. Eur J Biochem. 1975 Jun 16;55(1):105–110. doi: 10.1111/j.1432-1033.1975.tb02142.x. [DOI] [PubMed] [Google Scholar]
- Krebs H. A., Eggleston L. V. Metabolism of acetoacetate in animal tissues. 1. Biochem J. 1945;39(5):408–419. [PMC free article] [PubMed] [Google Scholar]
- Mangos J. A., McSherry N. R., Barber T., Arvanitakis S. N., Wagner V. Dispersed rat parotid acinar cells. II. Characterization of adrenergic receptors. Am J Physiol. 1975 Sep;229(3):560–565. doi: 10.1152/ajplegacy.1975.229.3.560. [DOI] [PubMed] [Google Scholar]
- Michell R. H. Inositol phospholipids and cell surface receptor function. Biochim Biophys Acta. 1975 Mar 25;415(1):81–47. doi: 10.1016/0304-4157(75)90017-9. [DOI] [PubMed] [Google Scholar]
- Michell R. H., Jones L. M. Enhanced phosphatidylinositol labelling in rat parotid fragments exposed to alpha-adrenergic stimulation. Biochem J. 1974 Jan;138(1):47–52. doi: 10.1042/bj1380047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oron Y., Lowe M., Selinger Z. Involvement of the alpha-adrenergic receptor in the phospholipid effect in rat parotid. FEBS Lett. 1973 Aug 15;34(2):198–200. doi: 10.1016/0014-5793(73)80792-6. [DOI] [PubMed] [Google Scholar]
- Thompson M. P., Williamson D. H. Metabolic interactions of glucose, acetoacetate and adrenaline in rat submaxillary gland in vitro. Biochem J. 1975 Mar;146(3):635–644. doi: 10.1042/bj1460635. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson M. P., Williamson D. H. The ability of the calcium ionophore A-23187 to mimic some of the effects of adrenaline on the metabolism of rat submaxillary gland. FEBS Lett. 1976 Feb 15;62(2):208–211. doi: 10.1016/0014-5793(76)80054-3. [DOI] [PubMed] [Google Scholar]
