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ATP-evoked membrane responses inXenopus oocytes

  • Excitable Tissues and Central Nervous Physiology
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Abstract

Voltage-clamp technique and intracellular injections of drugs were used to study the adenosine triphosphate (ATP)-evoked depolarizing current response in theXenopus laevis oocytes. The depolarizing current was comprised of a fast transient component (D1) followed by a late long-lasting component (D2). It was carried mainly by Cl ions. The depolarizing current was better elicited by ATP and ADP than by AMP or adenosine and was not blocked either by theophylline (0.2 mM) or by quinidine sulphate (1 mM). The D2 current was sometimes masked by an ATP-evoked K+ hyperpolarizing current which was blocked by theophylline and mediated via P1 purinoceptors. This study suggests that the oocyte's membrane embodies at least two different purinoceptor's types, each of these types subserves a different set of ionic channels.

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References

  • Barish ME (1983) A transient calcium-dependent chloride current in the immatureXenopus oocyte. J Physiol 342:309–325

    Google Scholar 

  • Barnard EA, Miledi R, Sumikawa K (1982) Translation of exogenous messenger RNA coding for nicotinic acetylcholine receptors produces junctional receptors inXenopus oocytes. Proc R Soc Lond (Biol) 215:241–246

    Google Scholar 

  • Bowman WC, Hall MT (1970) Inhibition of rabbit intestine mediated by alfa- and beta-adrenoceptors. Br J Pharmacol 38:399–415

    Google Scholar 

  • Burgess GM, Claret M, Jenkinson DH (1979) Effects of catecholamines, ATP and ionophore A23187 on potassium and calcium movements in isolated hepatocytes. Nature 279: 544–546

    Google Scholar 

  • Burnstock G (1978) A basis for distinguishing two types of purinergic receptor. In: Straub RW, Bolis L (eds) Cell membrane receptors for drugs and hormones: a multidisciplinary approach. Raven Press, New York, pp 107–118

    Google Scholar 

  • Burnstock G (1981) Neurotransmitters and trophic factors in the autonomic nervous system. J Physiol 313:1–34

    Google Scholar 

  • Burnstock G (1985) Purinergic mechanisms broaden their sphere of influence. TINS 1:5–6

    Google Scholar 

  • Dascal N, Landau EM (1980) Types of muscarinic responses inXenopus oocytes. Life Sci 27:1423–1428

    Google Scholar 

  • Dascal N, Landau EM (1982) Cyclic GMP mimics the muscarinic response inXenopus oocytes: identity of ionic mechanisms. Proc Natl Acad Sci USA 79:3052–3056

    Google Scholar 

  • Dascal N, Landau EM, Lass Y (1984)Xenopus oocytes resting potential, muscarinic responses and the role of calcium and guanosine 3′, 5′ cyclic monophosphate. J Physiol 352:551–574

    Google Scholar 

  • Dascal D, Gillo B, Lass Y (1985) Role of calcium mobilization in mediation of acetylcholine-evoked chloride currents inXenopus laevis oocytes. J Physiol 366:299–313

    Google Scholar 

  • Den Hertog A (1982) Calcium and the action of adrenaline, ATP and carbachol on guinea-pig taenia caeci. J Physiol 325: 423–439

    Google Scholar 

  • Dumont JN (1972) Oogenesis inXenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals. J Morphol 136:153–180

    Google Scholar 

  • Ferrero JD, Frischknecht R (1983) Different effector mechanisms for ATP and adenosine hyperpolarization in the guinea-pigTaenia coli. Eur J Pharmacol 87:151–154

    Google Scholar 

  • Gallacher DV (1982) Are there purinergic receptors on parotid acinar cells? Nature 296:83–86

    Google Scholar 

  • Goto M, Yatani A, Tsuda Y (1977) An analysis of the action of ATP and related compounds on membrane current tension components in bullfrog atrial muscle. Jpn J Physiol 27:81–94

    Google Scholar 

  • Gundersen CB, Miledi R, Parker I (1983) Serotonin receptors induced by exogenous messenger RNA inXenopus oocytes. Proc R Soc Lond (Biol) 219:103–109

    Google Scholar 

  • Hille B (1984) Ionic channels, of exitable membranes. Sinauer, MA, USA

    Google Scholar 

  • Hutter OF, Rankin AC (1982) Increase by adenosine and adenine nucleotides in potassium permeability of sinus venosus of tortoise heart. J Physiol 329:57p-58p

    Google Scholar 

  • Jager JP (1974) The effect of catecholamines and ATP on the smooth muscle cell membrane of the guinea-pig taenia coli. Eur J Pharmacol 25:372–382

    Google Scholar 

  • Kusano K, Miledi R, Stinnakre, J (1977) Acetylcholine receptors in the oocyte membrane. Nature 270:739–741

    Google Scholar 

  • Kusano K, Miledi R, Stinnakre J (1982) Cholinergic and catecholaminergic receptors in theXenopus oocytes membrane. J Physiol 328:143–170

    Google Scholar 

  • Lotan I, Dascal N, Cohen S, Lass Y (1982) Adenosine-induced slow ionic currents inXenopus oocytes. Nature 298:572–574

    Google Scholar 

  • Lotan I, Dascal N, Oron Y, Cohen S, Lass Y (1985) Adenosineinduced K+ current inXenopus oocytes and the role of adenosine 3′, 5′-monophosphate. Mol Pharmacol 28:170–177

    Google Scholar 

  • Meszaros J, Kelemen K, Kecskmeti V, Szegi J (1984) Antagonism between adenosine and bromobenzyl-methyl-adamantylamine, a K+ channel blocker in atrial myocardium of guinea pig. Eur J Pharmacol 98:265–268

    Google Scholar 

  • Miledi R (1982) A calcium-dependent transient outward current inXenopus laevis oocytes. Proc R Soc Lond (Biol) 215:491–497

    Google Scholar 

  • Miledi R, Parker I (1984) Chloride current induced, by injection of calcium intoXenopus oocytes. J Physiol 357:173–183

    Google Scholar 

  • Miledi R, Parker I, Sumikawa K (1982) Synthesis of chick brain GABA receptors by frog oocytes. Proc R Soc Lond (Biol) 216:509–515

    Google Scholar 

  • Mishina M, Kurosaki T, Tobimatsu T, Morimoto Y, Noda M, Yamamoto T, Terao M, Lindsrom J, Takahashi T, Kuno M, Numa S (1984) Expression of functional acetylcholine receptors from cloned cDNAs. Nature 307:604–608

    Google Scholar 

  • Okada Y, Yada T, Ohno-Shosaku T, Oiki S, Ueda S, Machida K (1984) Exogenous ATP induces electrical membrane responses in fibroblasts. Exp Cell Res 152:552–557

    Google Scholar 

  • Stone TW (1981) Differential blockade of ATP, noradrenaline and electrically-evoked constructions of the rat vas deferens by nifedipine. Eur J Pharmacol 74:373–376

    Google Scholar 

  • Tomita T, Watanabe H (1973) A comparison of the effects of adenosine triphosphate with noradrenaline and with the inhibitory potential of the guinea-pigTaenia coli. J Physiol 231:167–177

    Google Scholar 

  • Yatani A, Goto M, Tsuda Y (1978) Nature of catecholamine-like actions of ATP and other energy rich nucleotides on the bullfrog atrial muscle. Jpn J Physiol 28:47–61

    Google Scholar 

  • Yatani A, Tsuda Y, Brown AM (1982) Nanomolar concentrations of extracellular ATP activate membrane Ca2+ channel in snail neurons. Nature 296:169–171

    Google Scholar 

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Lotan, I., Dascal, N., Cohen, S. et al. ATP-evoked membrane responses inXenopus oocytes. Pflugers Arch. 406, 158–162 (1986). https://doi.org/10.1007/BF00586677

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  • DOI: https://doi.org/10.1007/BF00586677

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