Abstract
Simultaneous studies on the secretory response of amylase and the neurotransmitter receptors of rat parotid gland, after brief treatment with agonists, showed selective alteration in beta-adrenoceptors with specific change in amylase secretion, suggesting a regulatory role of the receptors in the secretory response. The beta-adrenergic agonist (+/-)-isoprenaline (IPR) stimulated amylase secretion from rat parotid tissues much more than did the same concentration of an alpha-adrenergic or cholinergic agonist. The stimulatory effects of IPR were studied by pre-treating rat parotid tissues with IPR for 10 min and then incubating the tissue in fresh medium for 10 min. Pre-treatment with 10 microM-IPR for 10 min resulted in increased amylase secretion during further incubation with IPR and also in a lower EC50 value of amylase secretion for IPR. This treatment also resulted in selective changes in the number and affinity of beta-adrenoceptors, assessed by measuring binding of [3H]dihydroalprenolol (DHA): the maximal binding sites increased from 286/357 f-mole to mg protein and the IC50 value (the concentration for 50% inhibition of specific [3H]DHA binding) of beta-agonists, not antagonists, decreased significantly. An increase in the period of pre-treatment with IPR to 30 min resulted in a decrease in the maximal binding sites of beta-adrenoceptors and a decrease in amylase secretion during further incubation with IPR. Experiments with other agonists showed that supersensitivity of the secretory response was induced specifically by beta-agonists. Binding studies with [3H]WB-4101 and [3H]quinuclidinyl benzilate showed that alpha-adrenoceptors and muscarinic ACh receptors in rat parotid did not change under the conditions tested. The alteration in beta-adrenoceptors was parallel with a change in amylase secretion after IPR pre-treatment, but not with a change in cyclic AMP content.
Full text
PDF











Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Arnett C. D., Davis J. N. Denervation-induced changes in alpha and beta adrenergic receptors of the rat submandibular gland. J Pharmacol Exp Ther. 1979 Nov;211(2):394–400. [PubMed] [Google Scholar]
- Au D. K., Malbon C. C., Butcher F. R. Identification and characterization of beta-adrenergic receptors in rat parotid membranes. Biochim Biophys Acta. 1977 Dec 22;500(2):361–371. doi: 10.1016/0304-4165(77)90027-7. [DOI] [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]
- Butcher F. R., Goldman J. A., Nemerovski Effect of adrenergic agents on alpha-amylase release and adenosine 3',5'-monophosphate accumulation in rat parotid tissue slices. Biochim Biophys Acta. 1975 May 5;392(1):82–94. doi: 10.1016/0304-4165(75)90168-3. [DOI] [PubMed] [Google Scholar]
- Butcher F. R., Thayer M., Goldman J. A. Effect of adenosine 3',5'-cyclic monophosphate derivatives on alpha-amylase release, protein kinase and cyclic nucleotide phosphodiesterase activity from rat parotid tissue. Biochim Biophys Acta. 1976 Feb 24;421(2):289–295. doi: 10.1016/0304-4165(76)90295-6. [DOI] [PubMed] [Google Scholar]
- Bylund D. B., Martinez J. R., Pierce D. L. Regulation of autonomic receptors in rat submandibular gland. Mol Pharmacol. 1982 Jan;21(1):27–35. [PubMed] [Google Scholar]
- Carlsö B., Danielsson A., Henriksson R., Idahl L. A. Dissociation of beta-adrenoceptor-induced effects on amylase secretion and cyclic adenosine 3', 5' monophosphate accumulation. Br J Pharmacol. 1982 Apr;75(4):633–638. doi: 10.1111/j.1476-5381.1982.tb09184.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cooper B., Handin R. I., Young L. H., Alexander R. W. Agonist regulation of the human platelet alpha-adrenergic receptor. Nature. 1978 Aug 17;274(5672):703–706. doi: 10.1038/274703a0. [DOI] [PubMed] [Google Scholar]
- Glaubiger G., Lefkowitz R. J. Elevated beta-adrenergic receptor number after chronic propranolol treatment. Biochem Biophys Res Commun. 1977 Sep 23;78(2):720–725. doi: 10.1016/0006-291x(77)90238-8. [DOI] [PubMed] [Google Scholar]
- Glaubiger G., Tsai B. S., Lefkowitz R. J., Weiss B., Johnson E. M., Jr Chronic guanethidine treatment increases cardiac beta-adrenergic receptors. Nature. 1978 May 18;273(5659):240–242. doi: 10.1038/273240a0. [DOI] [PubMed] [Google Scholar]
- Greenberg D. A., Prichard D. C., Snyder S. H. Alpha-noradrenergic receptor binding in mammalian brain: differential labeling of agonist and antagonist states. Life Sci. 1976 Jul 1;19(1):69–76. doi: 10.1016/0024-3205(76)90375-1. [DOI] [PubMed] [Google Scholar]
- Harborne A. J., Smith M. E. Agonist-induced potentiation of acetylcholine sensitivity in denervated skeletal muscle. Nature. 1979 Nov 1;282(5734):85–87. doi: 10.1038/282085a0. [DOI] [PubMed] [Google Scholar]
- Harper J. F., Brooker G. Amylase secretion from the rat parotid: refractoriness to muscarinic and adrenergic agonists. Mol Pharmacol. 1978 Nov;14(6):1031–1045. [PubMed] [Google Scholar]
- Hata F., Takeyasu K., Uchida S., Yoshida H. Increase in response and number of alpha-adrenoceptors of rat vas deferens on brief pretreatment with an alpha-agonist. Eur J Pharmacol. 1980 Oct 17;67(2-3):193–199. doi: 10.1016/0014-2999(80)90498-7. [DOI] [PubMed] [Google Scholar]
- Hata F., Uchida S., Takeyasu K., Ishida H., Yoshida H. Changes in alpha-adrenergic receptors in rat brain in vitro by preincubation with alpha-adrenergic ligands. Jpn J Pharmacol. 1980 Aug;30(4):570–574. doi: 10.1254/jjp.30.570. [DOI] [PubMed] [Google Scholar]
- Henriksson R. beta 1- and beta 2-adrenoceptor agonists have different effects on rat parotid acinar cells. Am J Physiol. 1982 May;242(5):G481–G485. doi: 10.1152/ajpgi.1982.242.5.G481. [DOI] [PubMed] [Google Scholar]
- Honma M., Satoh T., Takezawa J., Ui M. An ultrasensitive method for the simultaneous determination of cyclic AMP and cyclic GMP in small-volume samples from blood and tissue. Biochem Med. 1977 Dec;18(3):257–273. doi: 10.1016/0006-2944(77)90060-6. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Makman M. H. Properties of adenylate cyclase of lymphoid cells. Proc Natl Acad Sci U S A. 1971 May;68(5):885–889. doi: 10.1073/pnas.68.5.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mukherjee C., Caron M. G., Lefkowitz R. J. Catecholamine-induced subsensitivity of adenylate cyclase associated with loss of beta-adrenergic receptor binding sites. Proc Natl Acad Sci U S A. 1975 May;72(5):1945–1949. doi: 10.1073/pnas.72.5.1945. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roscher A. A., Wiesmann U. N., Honegger U. E. Changes in beta adrenergic receptors in submaxillary glands of chronically reserpine- or isoproterenol-treated rats. J Pharmacol Exp Ther. 1981 Feb;216(2):419–424. [PubMed] [Google Scholar]
- Sporn J. R., Harden T. K., Wolfe B. B., Molinoff P. B. beta-Adrenergic receptor involvement in 6-hydroxydopamine-induced supersensitivity in rat cerebral cortex. Science. 1976 Nov 5;194(4265):624–626. doi: 10.1126/science.10626. [DOI] [PubMed] [Google Scholar]
- Strittmatter W. J., Davis J. N., Lefkowitz R. J. alpha-Adrenergic receptors in rat parotid cells. II. Desensitization of receptor binding sites and potassium release. J Biol Chem. 1977 Aug 10;252(15):5478–5482. [PubMed] [Google Scholar]
- Talamo B. R., Adler S. C., Burt D. R. Parasympathetic denervation decreases muscarinic receptor binding in rat parotid. Life Sci. 1979 Apr 23;24(17):1573–1580. doi: 10.1016/0024-3205(79)90018-3. [DOI] [PubMed] [Google Scholar]
- U'Prichard D. C., Reisine T. D., Yamamura S., Mason S. T., Fibiger H. C., Ehlert F., Yamamura H. I. Differential supersensitivity of beta-receptor subtypes in rat cortex and cerebellum after central noradrenergic denervation. Life Sci. 1980 Feb 4;26(5):355–364. doi: 10.1016/0024-3205(80)90151-4. [DOI] [PubMed] [Google Scholar]
- Uchida S., Takeyasu K., Noguchi Y., Yoshida H., Hata T., Kita T. Decrease in muscarinic acetylcholine receptors in the small intestine of mice subjected to repeated cold stress. Life Sci. 1978 Jun 26;22(24):2197–2203. doi: 10.1016/0024-3205(78)90571-4. [DOI] [PubMed] [Google Scholar]
- Wojcik J. D., Grand R. J., Kimberg D. V. Amylase secretion by rabbit parotid gland. Role of cyclic AMP and cyclic GMP. Biochim Biophys Acta. 1975 Dec 5;411(2):250–262. doi: 10.1016/0304-4165(75)90305-0. [DOI] [PubMed] [Google Scholar]
- Yamamura H. I., Snyder S. H. Muscarinic cholinergic binding in rat brain. Proc Natl Acad Sci U S A. 1974 May;71(5):1725–1729. doi: 10.1073/pnas.71.5.1725. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yoshimura K., Nezu E., Chiba A. Stimulation of alpha-amylase release and cyclic AMP accumulation by catecholamine in rat parotid slices in vitro. Jpn J Physiol. 1982;32(1):121–135. doi: 10.2170/jjphysiol.32.121. [DOI] [PubMed] [Google Scholar]
- de Peusner I. C., Perec C. J., Stefano F. J. Effects of sympathectomy on the in vitro alpha and beta-responses of the parotid gland. Naunyn Schmiedebergs Arch Pharmacol. 1979 Sep;308(3):217–221. doi: 10.1007/BF00501385. [DOI] [PubMed] [Google Scholar]
- de Peusner I. C., Stefano F. J., Perec C. J. Effects of sympathectomy on the in vivo alpha and beta-responses of the parotid gland. Naunyn Schmiedebergs Arch Pharmacol. 1979 Sep;308(3):211–216. doi: 10.1007/BF00501384. [DOI] [PubMed] [Google Scholar]
