Abstract
1. Extracellular adenosine 5'-triphosphate (ATP) activated an early excitatory conductance followed by a late potassium conductance in developing chick skeletal muscle. A series of ATP analogues were tested for their ability to activate these two conductances. All compounds tested were either agonists for both responses or for neither. Furthermore, the potency of agonists was similar for the two responses. 2. The order of potency for agonists was ATP approximately adenosine 5'-O-(3-thiotriphosphate) (ATP-gamma-S) approximately 2-methylthio-ATP (2-CH3S-ATP) greater than 2'-deoxy-ATP approximately 3'-deoxy-ATP greater than adenosine 5'-tetraphosphate (ATP-OPO3) approximately adenosine 5'-diphosphate (ADP). Many other ATP analogues were not agonists. 3. Activation of the excitatory response did not require divalent cations. Furthermore, the concentration-response relation of the excitatory response was similar when ATP was applied as the free anion of ATP (ATP4-) or complexed with a divalent cation (M.ATP2-). 4. Three antagonists of the ATP response were characterized. 8-Br-ATP was a weak antagonist, while 2',3'-dialdehyde-ATP and DIDS (4,4'-diisocyanatostilbene-2,2'-disulphonic acid) were potent irreversible inhibitors. The two conductances were equally affected by these antagonists. 5. These results suggest that both ATP responses are activated through the same receptor type, or two very similar receptors.
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Selected References
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- Benham C. D., Tsien R. W. A novel receptor-operated Ca2+-permeable channel activated by ATP in smooth muscle. Nature. 1987 Jul 16;328(6127):275–278. doi: 10.1038/328275a0. [DOI] [PubMed] [Google Scholar]
- Cockcroft S., Gomperts B. D. Activation and inhibition of calcium-dependent histamine secretion by ATP ions applied to rat mast cells. J Physiol. 1979 Nov;296:229–243. doi: 10.1113/jphysiol.1979.sp013002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Young M. B., Scarpa A. Extracellular ATP induces Ca2+ transients in cardiac myocytes which are potentiated by norepinephrine. FEBS Lett. 1987 Oct 19;223(1):53–58. doi: 10.1016/0014-5793(87)80508-2. [DOI] [PubMed] [Google Scholar]
- Friel D. D., Bean B. P. Two ATP-activated conductances in bullfrog atrial cells. J Gen Physiol. 1988 Jan;91(1):1–27. doi: 10.1085/jgp.91.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gordon J. L. Extracellular ATP: effects, sources and fate. Biochem J. 1986 Jan 15;233(2):309–319. doi: 10.1042/bj2330309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
- Hume R. I., Honig M. G. Excitatory action of ATP on embryonic chick muscle. J Neurosci. 1986 Mar;6(3):681–690. doi: 10.1523/JNEUROSCI.06-03-00681.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hume R. I., Thomas S. A. A calcium- and voltage-dependent chloride current in developing chick skeletal muscle. J Physiol. 1989 Oct;417:241–261. doi: 10.1113/jphysiol.1989.sp017799. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hume R. I., Thomas S. A. Multiple actions of adenosine 5'-triphosphate on chick skeletal muscle. J Physiol. 1988 Dec;406:503–524. doi: 10.1113/jphysiol.1988.sp017393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Häggblad J., Heilbronn E. Externally applied adenosine-5'-triphosphate causes inositol triphosphate accumulation in cultured chick myotubes. Neurosci Lett. 1987 Feb 24;74(2):199–204. doi: 10.1016/0304-3940(87)90149-2. [DOI] [PubMed] [Google Scholar]
- Jahr C. E., Jessell T. M. ATP excites a subpopulation of rat dorsal horn neurones. Nature. 1983 Aug 25;304(5928):730–733. doi: 10.1038/304730a0. [DOI] [PubMed] [Google Scholar]
- Krishtal O. A., Marchenko S. M., Obukhov A. G. Cationic channels activated by extracellular ATP in rat sensory neurons. Neuroscience. 1988 Dec;27(3):995–1000. doi: 10.1016/0306-4522(88)90203-5. [DOI] [PubMed] [Google Scholar]
- Krishtal O. A., Marchenko S. M., Pidoplichko V. I. Receptor for ATP in the membrane of mammalian sensory neurones. Neurosci Lett. 1983 Jan 31;35(1):41–45. doi: 10.1016/0304-3940(83)90524-4. [DOI] [PubMed] [Google Scholar]
- McMillian M. K., Soltoff S. P., Lechleiter J. D., Cantley L. C., Talamo B. R. Extracellular ATP increases free cytosolic calcium in rat parotid acinar cells. Differences from phospholipase C-linked receptor agonists. Biochem J. 1988 Oct 1;255(1):291–300. [PMC free article] [PubMed] [Google Scholar]
- Motulsky H. J., Ransnas L. A. Fitting curves to data using nonlinear regression: a practical and nonmathematical review. FASEB J. 1987 Nov;1(5):365–374. [PubMed] [Google Scholar]
- Siggins G. R., Gruol D. L., Padjen A. L., Formans D. S. Purine and pyrimidine mononucleotides depolarise neurones of explanted amphibian sympathetic ganglia. Nature. 1977 Nov 17;270(5634):263–265. doi: 10.1038/270263a0. [DOI] [PubMed] [Google Scholar]
- Silinsky E. M., Hubbard J. I. Thermal synthesis of amino acids from a simulated primitive atmosphere. Nature. 1973 Jun 15;243(5407):404–405. doi: 10.1038/243404a0. [DOI] [PubMed] [Google Scholar]
- Thomas S. A., Hume R. I. Irreversible desensitization of ATP responses in developing chick skeletal muscle. J Physiol. 1990 Nov;430:373–388. doi: 10.1113/jphysiol.1990.sp018296. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas S. A., Hume R. I. Permeation of both cations and anions through a single class of ATP-activated ion channels in developing chick skeletal muscle. J Gen Physiol. 1990 Apr;95(4):569–590. doi: 10.1085/jgp.95.4.569. [DOI] [PMC free article] [PubMed] [Google Scholar]
