Skip to main content
Log in

Forskolin blocks carbachol-mediated ion-permeability of chick myotube nicotinic receptors and inhibits binding of 3H-phencyclidine to Torpedo microsac nicotinic receptors

  • Published:
Naunyn-Schmiedeberg's Archives of Pharmacology Aims and scope Submit manuscript

Summary

Forskolin, a commonly used adenylate cyclase activator, was found to inhibit reversibly the carbachol-induced ion-translocating capacity of the nicotinic acetylcholine receptor (nAChR) on chick myotubes in a dose- (IC50 = 20 μM) and time-dependent manner. This effect was not correlated to increases in cellular cAMP. Forskolin, at a concentration (50 μM) that totally blocked the carbachol-induced 86Rb influx, caused no change in carbachol or α-bungarotoxin binding to chick myotube nAChR in situ. In contrast, in the presence of carbachol, forskolin inhibited (IC50 = 10 μM) the binding of 3H-phencyclidine, a putative nAChR ion-channel ligand, to Torpedo microsac nAChR. Inhibition of 3H-phencyclidine binding in the absence of carbachol was not complete. Membrane leakage studies on myotubes, measuring 3H-efflux from 2-deoxy-d(1-3H)-glucose loaded cells and electrophysiological measurements of membrane properties supported the interpretation that forskolin induced decreases in plasma membrane permeability. In conclusion, forskolin blocks the carbachol-mediated increase in permeability of the nAChR channel by (1) binding to the ion-channel (open state) and (2) generally perturbing the plasma membrane function possibly by interfering with the protein-lipid interface.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aguayo LG, Witkop B, Albuquerque EX (1986) Voltage- and time-dependent effects of phencyclidines on the endplate current arise from open and closed channel blockade. Proc Natl Acad Sci USA 83:3523–3527

    Google Scholar 

  • Albuquerque EX, Eldefrawi AT, Eldefrawi ME, Mansour NA, Tsai M-C (1978) Amantadine: Neuromuscular blockade by suppression of ionic conductance of the acetylcholine receptor. Science 199:788–790

    Google Scholar 

  • Albuquerque EX, Tsai M-C, Aronstam RS, Eldefrawi AT, Eldefrawi ME (1980) Sites of action of phencyclidine. II. Interaction with the ionic channel of the nicotinic receptor. Mol Pharmacol 18:167–178

    Google Scholar 

  • Albuquerque EX, Deshpande SS, Aracava Y, Alkondon M, Daly JW (1986) A possible involvement of cyclic AMP in the expression of desensitization of the nicotinic acetylcholine receptor. FEBS Lett 199:113–120

    Google Scholar 

  • Catterall WA (1975) Sodium transport by the acetylcholine receptor of cultured muscle cells. J Biol Chem 250:1776–1781

    Google Scholar 

  • Eldefrawi ME, Eldefrawi AT, Aronstam RS, Maleque M, Warnick JE, Albuquerque EX (1980) 3H-phencyclidine: A probe for the ionic channel of the nicotinic receptor. Proc Natl Acad Sci USA 77:7458–7462

    Google Scholar 

  • Eldefrawi AT, Miller ER, Murphy DL, Eldefrawi ME (1982) 3H-phencyclidine interactions with the nicotinic acetylcholine receptor channel and its inhibition by psychotropic, antipsychotic, opiate, antidepressant, antibiotic, antiviral and antiarrhythmic drugs. Mol Pharmacol 22:72–81

    Google Scholar 

  • Häggblad J, Eriksson H, Heilbronn E (1985) Oxotremorine acts as a partial nicotinic agonist on cultured chick myotubes. Acta Pharmacol Toxicol (Copenh) 57:317–321

    Google Scholar 

  • Hedlund B, Århem P, Lorentz M, Sydbom A (1986) Non-muscarinic effects of scopolamine on N1E-115 neuroblastoma cells. Acta Physiol Scand (in press)

  • Heidmann T, Oswald RE, Changeux J-P (1983) Multiple sites of action of noncompetitive blockers on acetylcholine receptor-rich membrane fragments from Torpedo marmorata. Biochemistry 22:3112–3127

    Google Scholar 

  • Heilbronn E, Eriksson H, Häggblad J (1986) cAMP-dependent phosphorylation of the nicotinic acetylcholine receptor: characterization of the protein kinase in Torpedo electric organ, lack of correlation in myotubes between increased levels of cAMP and influx of monovalent ions, block of influx by forskolin independently of cAMP-levels. In: Maelicke E (ed) Nicotinic acetylcholine receptor: Structure and function. Springer, Berlin Heidelberg New York, pp 291–303

    Google Scholar 

  • Lindstrom J, Einarson B, Tzartos S (1981) Production and assay of antibodies to the acetylcholine receptors. In: Langone SS, Van Vunakis H (eds) Methods in enzymology, vol 74. Academic Press, New York, pp 432–460

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    Google Scholar 

  • Manning AS, Kinoshita K, Buschmans E, Coltart DJ, Hearse DJ (1985) The genesis of arrhythmias during myocardial ischaemia. Dissociation between changes in cyclic adenosine monophosphate and electrical instability in the rat. Circ Res 57:668–675

    Google Scholar 

  • McHugh EM, McGee R Jr (1986) Direct anaesthetic-like effects of forskolin on the nicotinic acetylcholine receptors of PC 12 cells. J Biol Chem 261:3103–3106

    Google Scholar 

  • Middleton P, Jaramillo F, Schuetze SM (1986) Forskolin increases the rate of acetylcholine receptor desensitization at rat soleus endplates. Proc Natl Acad Sci USA 83:4967–4971

    Google Scholar 

  • Nastuk WL, Su PC, Doubilet P (1976) Anticholinergic activities of amantadine in neuromuscular transmission. Nature 264:76–79

    Google Scholar 

  • Oswald RE (1983) Effects of calcium on the binding of phencyclidine to acetylcholine receptor-rich membrane fragments from Torpedo californica electroplaque. J Neurochem 41: 1077–1084

    Google Scholar 

  • Oswald RE, Changeux J-P (1981) Ultraviolet light-induced labeling by non-competitive blockers of the acetylcholine receptor from Torpedo marmorata. Proc Natl Acad Sci USA 78:3925–3929

    Google Scholar 

  • Oswald RE, Heidmann T, Changeux JP (1983) Multiple affinity states for noncompetitive blockers revealed by 3H-phencyclidine binding to acetylcholine receptor rich membrane fragments from Torpedo marmorata. Biochemistry 22:3128–3136

    Google Scholar 

  • Schimerlik M, Quast U, Raftery MA (1979) Ligand induced changes in membrane-bound acetylcholine receptor observed by ethidium fluorescence. 1. Equilibrium studies. Biochemistry 18:1884–1890

    Google Scholar 

  • Seamon KB, Daly JW (1983) Forskolin, cyclic AMP and cellular physiology. Trends Pharmacol Sci 4:120–123

    Google Scholar 

  • Walum E (1982) Membrane lesions in cultured mouse neuroblastoma cells exposed to metal compounds. Toxicology 25:67–74

    Google Scholar 

  • Warnick JE, Maleque MA, Bakry N, Eldefrawi AT, Albuquerque EX (1982) Structure-activity relationships of amantadine. I. Interaction of the N-alkyl analogues with the ionic channels of the nicotinic acetylcholine receptor and electrically excitable membrane. Mol Pharmacol 22:82–93

    Google Scholar 

  • Whetton AD, Needham L, Dodd NJF, Heyworth CM, Houslay MD (1983) Forskolin and ethanol both perturb the structure of liver plasma membranes and activate adenylate cyclase. Biochem Pharmacol 32:1601–1608

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Send offprint requests to Johan Haggblad

Rights and permissions

Reprints and permissions

About this article

Cite this article

Häggblad, J., Eriksson, H., Hedlund, B. et al. Forskolin blocks carbachol-mediated ion-permeability of chick myotube nicotinic receptors and inhibits binding of 3H-phencyclidine to Torpedo microsac nicotinic receptors. Naunyn-Schmiedeberg's Arch Pharmacol 336, 381–386 (1987). https://doi.org/10.1007/BF00164869

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00164869

Key words

Navigation