Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1985 Dec;86(4):827–836. doi: 10.1111/j.1476-5381.1985.tb11104.x

The effects of adrenoceptor agonists and antagonists on plasma potassium concentration in anaesthetized guinea-pigs, rabbits and rats.

R A Coats
PMCID: PMC1916631  PMID: 4075019

Abstract

An intravenous K+-sensitive electrode has been used to monitor plasma [K+] changes induced by alpha- and beta-adrenoceptor agonists in anaesthetized guinea-pigs, rabbits and rats. The effects of phentolamine and propranolol on these responses were studied. In the guinea-pig both alpha- and beta-adrenoceptor agonists produced a biphasic response consisting of an initial rapid increase in [K+] which was followed, within 1 min, by a fall below baseline. The antagonist studies indicated that in this species both phases of the response could be elicited by either alpha- or beta-adrenoceptor activation. In the rabbit the responses were both slower and smaller than those seen in the guinea-pig and required larger agonist doses. In addition it was found that the increase in plasma [K+] was alpha-adrenoceptor-mediated while the subsequent fall was seen only with beta-adrenoceptor activation. In the rat triphasic changes in plasma [K+] were seen consisting of an initial decrease which was alpha-adrenoceptor-mediated, followed by an increase and then a second fall which was elicited by beta-adrenoceptor stimulation. The increase in plasma [K+] was only slightly reduced by either alpha- or beta-adrenoceptor antagonists. Apamin, a toxin from bee venom which blocks Ca2+-activated K+-channels, was found to block the hyperkalaemic phase of the response in the guinea-pig and rabbit but had no effect in the rat. It is concluded that there are marked species differences in the effects of adrenoceptor agonists on plasma [K+] in vivo.

Full text

PDF
827

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Banks B. E., Brown C., Burgess G. M., Burnstock G., Claret M., Cocks T. M., Jenkinson D. H. Apamin blocks certain neurotransmitter-induced increases in potassium permeability. Nature. 1979 Nov 22;282(5737):415–417. doi: 10.1038/282415a0. [DOI] [PubMed] [Google Scholar]
  2. Becker J., Jakob A. alpha-Adrenergic stimulation of glycolysis and Na+, K+-transport in perfused rat liver. Eur J Biochem. 1982 Nov 15;128(2-3):293–296. doi: 10.1111/j.1432-1033.1982.tb06964.x. [DOI] [PubMed] [Google Scholar]
  3. Burgess G. M., Claret M., Jenkinson D. H. Effects of quinine and apamin on the calcium-dependent potassium permeability of mammalian hepatocytes and red cells. J Physiol. 1981 Aug;317:67–90. doi: 10.1113/jphysiol.1981.sp013814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Burgess G. M., Giraud F., Poggioli J., Claret M. Alpha-adrenergically mediated changes in membrane lipid fluidity and Ca2/ binding in isolated rat liver plasma membranes. Biochim Biophys Acta. 1983 Jun 23;731(3):387–396. doi: 10.1016/0005-2736(83)90033-0. [DOI] [PubMed] [Google Scholar]
  5. CRAIG A. B., Jr Observations on epinephrine and glucagon-induced glycogenolysis and potassium loss in the isolated perfused frog liver. Am J Physiol. 1958 May;193(2):425–430. doi: 10.1152/ajplegacy.1958.193.2.425. [DOI] [PubMed] [Google Scholar]
  6. Capiod T., Berthon B., Poggioli J., Burgess G. M., Claret M. The effect of Ca2+ -mobilising hormones on the Na+ --K+ pump in isolated rat liver hepatocytes. FEBS Lett. 1982 May 3;141(1):49–52. doi: 10.1016/0014-5793(82)80013-6. [DOI] [PubMed] [Google Scholar]
  7. Castro-Tavares J. A comparison between the influence of pindolol and propranolol on the response of plasma potassium to catecholamines. Arzneimittelforschung. 1976 Feb;26(2):238–241. [PubMed] [Google Scholar]
  8. Castro-Tavares J. Effects of isoprenaline and phenylephrine on plasma potassium: role of the liver. Arch Int Pharmacodyn Ther. 1975 Nov;218(1):110–119. [PubMed] [Google Scholar]
  9. Castro-Travares J., Cardoso W. Effects of adrenergic stimulant and blocking drugs on the release and uptake of potassium by the liver. Arch Int Pharmacodyn Ther. 1974 May;209(1):100–112. [PubMed] [Google Scholar]
  10. Coats R. A. Effects of apamin on alpha-adrenoceptor-mediated changes in plasma potassium in guinea-pigs. Br J Pharmacol. 1983 Nov;80(3):573–580. doi: 10.1111/j.1476-5381.1983.tb10731.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Cocks T. M., Jenkinson D. H., Koller K. Interactions between receptors that increase cytosolic calcium and cyclic AMP in guinea-pig liver cells. Br J Pharmacol. 1984 Sep;83(1):281–291. doi: 10.1111/j.1476-5381.1984.tb10144.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. D'Silva J. L. The action of adrenaline on serum potassium. J Physiol. 1936 Feb 8;86(2):219–228. doi: 10.1113/jphysiol.1936.sp003356. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. ELLIS S., BECKETT S. B. MECHANISM OF THE POTASSIUM MOBILIZING ACTION OF EPINEPHRINE AND GLUCAGON. J Pharmacol Exp Ther. 1963 Dec;142:318–326. [PubMed] [Google Scholar]
  14. El-Refai M. F., Blackmore P. F., Exton J. H. Evidence for two alpha-adrenergic binding sites in liver plasma membranes. Studies with [3H]epinephrine and [3H]dihydroergocryptine. J Biol Chem. 1979 Jun 10;254(11):4375–4386. [PubMed] [Google Scholar]
  15. Haylett D. G., Jenkinson D. H. Effects of noradrenaline on potassium reflux, membrane potential and electrolyte levels in tissue slices prepared from guinea-pig liver. J Physiol. 1972 Sep;225(3):721–750. doi: 10.1113/jphysiol.1972.sp009966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Jakob A., Diem S. Metabolic responses of perfused rat livers to alpha- and beta-adrenergic agonists, glucagon and cyclic AMP. Biochim Biophys Acta. 1975 Sep 8;404(1):57–66. doi: 10.1016/0304-4165(75)90147-6. [DOI] [PubMed] [Google Scholar]
  17. Jenkinson D. H., Koller K. Interactions between the effects of alpha- and beta-adrenoceptor agonists and adenine nucleotides on the membrane potential of cells in guinea-pig liver slices. Br J Pharmacol. 1977 Jan;59(1):163–175. doi: 10.1111/j.1476-5381.1977.tb06991.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kvam D. C., Riggilo D. A., Lish P. M. Effect of some new beta-adrenergic blocking agents on certain metabolic responses to catecholamines. J Pharmacol Exp Ther. 1965 Aug;149(2):183–192. [PubMed] [Google Scholar]
  19. Lim M., Linton R. A., Band D. M. Continuous intravascular monitoring of epinephrine-induced changes in plasma potassium. Anesthesiology. 1982 Oct;57(4):272–278. doi: 10.1097/00000542-198210000-00004. [DOI] [PubMed] [Google Scholar]
  20. O'BRIEN G. S., EID C. H., MURPHY Q. R., Jr, MEEK W. J. Effect of elimination of hepatic circulation on cyclopropane-epinephrine ventricular tachycardia and arterial plasma potassium in dogs. J Pharmacol Exp Ther. 1954 Nov;112(3):374–377. [PubMed] [Google Scholar]
  21. Todd E. P., Vick R. L. Kalemotropic effect of epinephrine: analysis with adrenergic agonists and antagonists. Am J Physiol. 1971 Jun;220(6):1964–1969. doi: 10.1152/ajplegacy.1971.220.6.1964. [DOI] [PubMed] [Google Scholar]
  22. Tsujimoto A., Tanino S., Kaniike K., Seto K., Kurogochi Y. Relationship of hyperkalemic response to hepatic phosphorylase activation induced by adrenaline. Jpn J Pharmacol. 1965 Dec;15(4):423–428. doi: 10.1254/jjp.15.423. [DOI] [PubMed] [Google Scholar]
  23. Vick R. L., Todd E. P., Luedke D. W. Epinephrine-induced hypokalemia: relation to liver and skeletal muscle. J Pharmacol Exp Ther. 1972 Apr;181(1):139–146. [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES