Abstract
Acetylcholine (AcCho) elicits four distinct membrane responses in Xenopus oocytes; the responses can be studied by using the voltage clamp technique. The fastest of the responses, a transient inward current (D1 response), is muscarinic, being evoked by oxotremorine and blocked by atropine but not by curare or hexamethonium. The action of AcCho is cooperative, three transmitter-receptor complexes being required to cause a membrane conductance change, and the dose-response curve in most cases can be fitted by an equation assuming the existence of two binding sites with an affinity ratio of about 11. Guanosine 3',5'-cyclic monophosphate and the 8-bromo and dibutyryl derivatives cause a response similar to D1 in both its time course and the underlying ionic mechanism. The nucleotide-generated response has a smaller amplitude than the AcCho-generated D1.
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Selected References
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- Anderson C. R., Stevens C. F. Voltage clamp analysis of acetylcholine produced end-plate current fluctuations at frog neuromuscular junction. J Physiol. 1973 Dec;235(3):655–691. doi: 10.1113/jphysiol.1973.sp010410. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beam K. G., Greengard P. Cyclic nucleotides, protein phosphorylation and synaptic function. Cold Spring Harb Symp Quant Biol. 1976;40:157–168. doi: 10.1101/sqb.1976.040.01.017. [DOI] [PubMed] [Google Scholar]
- Beavo J. A., Hardman J. G., Sutherland E. W. Stimulation of adenosine 3',5'-monophosphate hydrolysis by guanosine 3',5'-monophosphate. J Biol Chem. 1971 Jun 25;246(12):3841–3846. [PubMed] [Google Scholar]
- Birdsall N. J., Burgen A. S., Hulme E. C. The binding of agonists to brain muscarinic receptors. Mol Pharmacol. 1978 Sep;14(5):723–736. [PubMed] [Google Scholar]
- Birdsall N. J., Hulme E. C., Burgen A. The character of the muscarinic receptors in different regions of the rat brain. Proc R Soc Lond B Biol Sci. 1980 Feb 13;207(1166):1–12. doi: 10.1098/rspb.1980.0011. [DOI] [PubMed] [Google Scholar]
- Bolton T. B. Rate of offset of action of slow-acting muscarinic antagonists is fast. Nature. 1977 Nov 24;270(5635):354–356. doi: 10.1038/270354a0. [DOI] [PubMed] [Google Scholar]
- Clark A. J. The antagonism of acetyl choline by atropine. J Physiol. 1926 Aug 6;61(4):547–556. doi: 10.1113/jphysiol.1926.sp002315. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dascal N., Landau E. M. Types of muscarinic response in Xenopus oocytes. Life Sci. 1980 Oct 13;27(15):1423–1428. doi: 10.1016/0024-3205(80)90407-5. [DOI] [PubMed] [Google Scholar]
- Dodge F. A., Jr, Rahamimoff R. Co-operative action a calcium ions in transmitter release at the neuromuscular junction. J Physiol. 1967 Nov;193(2):419–432. doi: 10.1113/jphysiol.1967.sp008367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dumont J. N. Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals. J Morphol. 1972 Feb;136(2):153–179. doi: 10.1002/jmor.1051360203. [DOI] [PubMed] [Google Scholar]
- Galper J. B., Klein W., Catterall W. A. Muscarinic acetylcholine receptors in developing chick heart. J Biol Chem. 1977 Dec 10;252(23):8692–8699. [PubMed] [Google Scholar]
- Goldberg N. D., Haddox M. K., Nicol S. E., Glass D. B., Sanford C. H., Kuehl F. A., Jr, Estensen R. Biologic regulation through opposing influences of cyclic GMP and cyclic AMP: the Yin Yang hypothesis. Adv Cyclic Nucleotide Res. 1975;5:307–330. [PubMed] [Google Scholar]
- Greengard P. Phosphorylated proteins as physiological effectors. Science. 1978 Jan 13;199(4325):146–152. doi: 10.1126/science.22932. [DOI] [PubMed] [Google Scholar]
- Hartzell H. C., Kuffler S. W., Stickgold R., Yoshikami D. Synaptic excitation and inhibition resulting from direct action of acetylcholine on two types of chemoreceptors on individual amphibian parasympathetic neurones. J Physiol. 1977 Oct;271(3):817–846. doi: 10.1113/jphysiol.1977.sp012027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hashiguchi T., Ushiyama N. S., Kobayashi H., Libet B. Does cyclic GMP mediate the slow excitatory synaptic potential in sympathetic ganglia? Nature. 1978 Jan 19;271(5642):267–268. doi: 10.1038/271267a0. [DOI] [PubMed] [Google Scholar]
- Kupfermann I. Role of cyclic nucleotides in excitable cells. Annu Rev Physiol. 1980;42:629–641. doi: 10.1146/annurev.ph.42.030180.003213. [DOI] [PubMed] [Google Scholar]
- Kusano K., Miledi R., Stinnakre J. Acetylcholine receptors in the oocyte membrane. Nature. 1977 Dec 22;270(5639):739–741. doi: 10.1038/270739a0. [DOI] [PubMed] [Google Scholar]
- McAfee D. A., Greengard P. Adenosine 3',5'-monophosphate: electrophysiological evidence for a role in synaptic transmission. Science. 1972 Oct;178(58):310–312. doi: 10.1126/science.178.4058.310. [DOI] [PubMed] [Google Scholar]
- Meyer R. B., Jr, Miller J. P. Analogs of cyclic AMP and cyclic GMP: general methods of synthesis and the relationship of structure to enzymic activity. Life Sci. 1974 Mar 16;14(6):1019–1040. doi: 10.1016/0024-3205(74)90228-8. [DOI] [PubMed] [Google Scholar]
- Nawrath H. Cyclic AMP and cyclic GMP may play opposing roles in influencing force of contraction in mammalian myocardium. Nature. 1976 Aug 5;262(5568):509–511. doi: 10.1038/262509b0. [DOI] [PubMed] [Google Scholar]
- Nawrath H. Does cyclic GMP mediate the negative inotropic effect of acetylcholine in the heart? Nature. 1977 May 5;267(5606):72–74. doi: 10.1038/267072a0. [DOI] [PubMed] [Google Scholar]
- Pott L. On the time course of the acetylcholine-induced hyperpolarization in quiescent guinea-pig atria. Pflugers Arch. 1979 May 15;380(1):71–77. doi: 10.1007/BF00582615. [DOI] [PubMed] [Google Scholar]
- Pott L., Pusch H. A kinetic model for the muscarinic action of acetylcholine. Pflugers Arch. 1979 Dec;383(1):75–77. doi: 10.1007/BF00584478. [DOI] [PubMed] [Google Scholar]
- Rodbell M. The role of hormone receptors and GTP-regulatory proteins in membrane transduction. Nature. 1980 Mar 6;284(5751):17–22. doi: 10.1038/284017a0. [DOI] [PubMed] [Google Scholar]
- Woody C. D., Swartz B. E., Gruen E. Effects of acetylcholine and cyclic GMP on input resistance of cortical neurons in awake cats. Brain Res. 1978 Dec 15;158(2):373–395. doi: 10.1016/0006-8993(78)90682-0. [DOI] [PubMed] [Google Scholar]
