Abstract
1. A whole-cell voltage-clamp technique has been used to study the alpha-effects of the adrenergic agonists noradrenaline, methoxamine and phenylephrine on the action potentials and membrane currents of rabbit atrial myocytes. Experiments were carried out at 22-23 degrees C. 2. In the presence of 10(-6) M-propranolol, all three agents prolonged action potential duration. This change could be ascribed principally to changes in membrane current early during the plateau phase of the action potential. In the presence of 10(-3) M-4-aminopyridine, no changes in calcium current (ICa) were observed on exposure to alpha-agonists. No significant shift in the voltage dependence or change in the amplitude of the calcium current-voltage relation was observed. 3. Exposure to 3 x 10(-4) M-CdCl2 to block ICa reduced the action potential prolongation caused by alpha-adrenergic agonists. Measurement of unloaded cell shortening revealed that action potential prolongation caused by alpha-agonists, especially at low stimulus rates, could contribute significantly to the positive inotropic effect of alpha-adrenoceptor stimulation. 4. The voltage-activated transient outward current (It) was markedly reduced during exposure to alpha-adrenergic agonists in a dose-dependent manner in the presence of CdCl2 (3 x 10(-4) M) and propranolol in sufficient concentration to prevent beta-adrenoceptor activation. Noradrenaline exhibited a higher potency for this effect than either methoxamine or phenylephrine. The noradrenaline concentration required to give 50% of the maximal effect was 6 x 10(-6) M compared with 2.3 x 10(-4) M for methoxamine. Noradrenaline reduced It by only about 60% of the maximum reduction produced by methoxamine suggesting that it could be classified as a partial agonist for this effect. 5. The reduction of It during exposure to alpha-adrenergic agonists was rate dependent in that larger current reductions were observed at very low rates of stimulation (less than 0.1 Hz). 6. The magnitudes of current-voltage relations for It were reduced over the entire voltage range studied during exposure to alpha-adrenergic agonists and reductions were dose dependent. No shift of these relations along the voltage axis was observed. 7. The steady-state inactivation relations for It were studied using two voltage clamp protocols. A two-step method resulted in a relatively steep sigmoid 'quasi-steady-state' relation. The half-inactivation potential of -27 mV was unaffected by alpha-adrenergic agonists.(ABSTRACT TRUNCATED AT 400 WORDS)
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Selected References
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- Aghajanian G. K. Modulation of a transient outward current in serotonergic neurones by alpha 1-adrenoceptors. Nature. 1985 Jun 6;315(6019):501–503. doi: 10.1038/315501a0. [DOI] [PubMed] [Google Scholar]
- Benfey B. G. Cardiac alpha adrenoceptors. Can J Physiol Pharmacol. 1980 Oct;58(10):1145–1157. doi: 10.1139/y80-174. [DOI] [PubMed] [Google Scholar]
- Benfey B. G. Function of myocardial alpha-adrenoceptors. Life Sci. 1982 Jul 12;31(2):101–112. doi: 10.1016/0024-3205(82)90421-0. [DOI] [PubMed] [Google Scholar]
- Benfey B. G., Varma D. R. Interactions of sympathomimetic drugs, propranolol and phentolamine, on atrial refractory period and contractility. Br J Pharmacol Chemother. 1967 Aug;30(3):603–611. doi: 10.1111/j.1476-5381.1967.tb02166.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brückner R., Meyer W., Mügge A., Schmitz W., Scholz H. Alpha-adrenoceptor-mediated positive inotropic effect of phenylephrine in isolated human ventricular myocardium. Eur J Pharmacol. 1984 Apr 6;99(4):345–347. doi: 10.1016/0014-2999(84)90144-4. [DOI] [PubMed] [Google Scholar]
- Brückner R., Mügge A., Scholz H. Existence and functional role of alpha 1-adrenoceptors in the mammalian heart. J Mol Cell Cardiol. 1985 Jul;17(7):639–645. doi: 10.1016/s0022-2828(85)80063-8. [DOI] [PubMed] [Google Scholar]
- Brückner R., Scholz H. Effects of alpha-adrenoceptor stimulation with phenylephrine in the presence of propranolol on force of contraction, slow inward current and cyclic AMP content in the bovine heart. Br J Pharmacol. 1984 May;82(1):223–232. doi: 10.1111/j.1476-5381.1984.tb16462.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Endoh M., Blinks J. R. Actions of sympathomimetic amines on the Ca2+ transients and contractions of rabbit myocardium: reciprocal changes in myofibrillar responsiveness to Ca2+ mediated through alpha- and beta-adrenoceptors. Circ Res. 1988 Feb;62(2):247–265. doi: 10.1161/01.res.62.2.247. [DOI] [PubMed] [Google Scholar]
- Endoh M., Schümann H. J. Frequency-dependence of the positive inotropic effect of methoxamine and naphazoline mediated by alpha-Adrenoceptors in the isolated rabbit papillary muscle. Naunyn Schmiedebergs Arch Pharmacol. 1975;287(4):377–389. doi: 10.1007/BF00500039. [DOI] [PubMed] [Google Scholar]
- Giles W. R., Imaizumi Y. Comparison of potassium currents in rabbit atrial and ventricular cells. J Physiol. 1988 Nov;405:123–145. doi: 10.1113/jphysiol.1988.sp017325. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giles W. R., van Ginneken A. C. A transient outward current in isolated cells from the crista terminalis of rabbit heart. J Physiol. 1985 Nov;368:243–264. doi: 10.1113/jphysiol.1985.sp015856. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giotti A., Ledda F., Mannaioni P. F. Effects of noradrenaline and isoprenaline, in combination with - and -receptor blocking substances, on the action potential of cardiac Purkinje fibres. J Physiol. 1973 Feb;229(1):99–113. doi: 10.1113/jphysiol.1973.sp010129. [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]
- Hescheler J., Nawrath H., Tang M., Trautwein W. Adrenoceptor-mediated changes of excitation and contraction in ventricular heart muscle from guinea-pigs and rabbits. J Physiol. 1988 Mar;397:657–670. doi: 10.1113/jphysiol.1988.sp017024. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hilgemann D. W. Extracellular calcium transients and action potential configuration changes related to post-stimulatory potentiation in rabbit atrium. J Gen Physiol. 1986 May;87(5):675–706. doi: 10.1085/jgp.87.5.675. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hiramoto T., Kushida H., Endoh M. Further characterization of the myocardial alpha-adrenoceptors mediating positive inotropic effects in the rabbit myocardium. Eur J Pharmacol. 1988 Aug 2;152(3):301–310. doi: 10.1016/0014-2999(88)90725-x. [DOI] [PubMed] [Google Scholar]
- Kimura J., Miyamae S., Noma A. Identification of sodium-calcium exchange current in single ventricular cells of guinea-pig. J Physiol. 1987 Mar;384:199–222. doi: 10.1113/jphysiol.1987.sp016450. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kushida H., Hiramoto T., Satoh H., Endoh M. Phorbol ester does not mimic, but antagonizes the alpha-adrenoceptor-mediated positive inotropic effect in the rabbit papillary muscle. Naunyn Schmiedebergs Arch Pharmacol. 1988 Feb;337(2):169–176. doi: 10.1007/BF00169245. [DOI] [PubMed] [Google Scholar]
- Leatherman G. F., Kim D., Smith T. W. Effect of phorbol esters on contractile state and calcium flux in cultured chick heart cells. Am J Physiol. 1987 Jul;253(1 Pt 2):H205–H209. doi: 10.1152/ajpheart.1987.253.1.H205. [DOI] [PubMed] [Google Scholar]
- McGrath J., Wilson V. Alpha-adrenoceptor subclassification by classical and response-related methods: same question, different answers. Trends Pharmacol Sci. 1988 May;9(5):162–165. doi: 10.1016/0165-6147(88)90030-2. [DOI] [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]
- Nakashima M., Tsuru H., Shigei T. Stimulant action of methoxamine in the isolated atria of normal and 6-propyl-2-thiouracil-fed rats. Jpn J Pharmacol. 1973 Jun;23(3):307–312. doi: 10.1254/jjp.23.307. [DOI] [PubMed] [Google Scholar]
- Nakayama T., Fozzard H. A. Adrenergic modulation of the transient outward current in isolated canine Purkinje cells. Circ Res. 1988 Jan;62(1):162–172. doi: 10.1161/01.res.62.1.162. [DOI] [PubMed] [Google Scholar]
- Pappano A. J. Propranolol-insensitive effects of epinephrine on action potential repolarization in electrically driven atria of the guinea pig. J Pharmacol Exp Ther. 1971 Apr;177(1):85–95. [PubMed] [Google Scholar]
- Poggioli J., Sulpice J. C., Vassort G. Inositol phosphate production following alpha 1-adrenergic, muscarinic or electrical stimulation in isolated rat heart. FEBS Lett. 1986 Oct 6;206(2):292–298. doi: 10.1016/0014-5793(86)80999-1. [DOI] [PubMed] [Google Scholar]
- Rabinowitz B., Chuck L., Kligerman M., Parmley W. W. Positive inotropic effects of methoxamine: evidence for alpha-adrenergic receptors in ventricular myocardium. Am J Physiol. 1975 Sep;229(3):582–585. doi: 10.1152/ajplegacy.1975.229.3.582. [DOI] [PubMed] [Google Scholar]
- Scholz J., Schaefer B., Schmitz W., Scholz H., Steinfath M., Lohse M., Schwabe U., Puurunen J. Alpha-1 adrenoceptor-mediated positive inotropic effect and inositol trisphosphate increase in mammalian heart. J Pharmacol Exp Ther. 1988 Apr;245(1):327–335. [PubMed] [Google Scholar]
- Schümann H. J., Wagner J., Knorr A., Reidemeister J. C., Sadony V., Schramm G. Demonstration in human atrial preparations of alpha-adrenoceptors mediating positive inotropic effects. Naunyn Schmiedebergs Arch Pharmacol. 1978 May;302(3):333–336. doi: 10.1007/BF00508304. [DOI] [PubMed] [Google Scholar]
- Shah A., Cohen I. S., Rosen M. R. Stimulation of cardiac alpha receptors increases Na/K pump current and decreases gK via a pertussis toxin-sensitive pathway. Biophys J. 1988 Aug;54(2):219–225. doi: 10.1016/S0006-3495(88)82950-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shibata E. F., Drury T., Refsum H., Aldrete V., Giles W. Contributions of a transient outward current to repolarization in human atrium. Am J Physiol. 1989 Dec;257(6 Pt 2):H1773–H1781. doi: 10.1152/ajpheart.1989.257.6.H1773. [DOI] [PubMed] [Google Scholar]
- Steadman B. W., Moore K. B., Spitzer K. W., Bridge J. H. A video system for measuring motion in contracting heart cells. IEEE Trans Biomed Eng. 1988 Apr;35(4):264–272. doi: 10.1109/10.1375. [DOI] [PubMed] [Google Scholar]
- Tanaka I., Tosaka T., Saito K., Shimura H., Saito T. Changes in the configuration of the rabbit atrial action potential after various periods of rest. Jpn J Physiol. 1967 Oct 15;17(5):487–504. doi: 10.2170/jjphysiol.17.487. [DOI] [PubMed] [Google Scholar]
- Wagner J., Brodde O. E. On the presence and distribution of alpha-adrenoceptors in the heart of various mammalian species. Naunyn Schmiedebergs Arch Pharmacol. 1978 May;302(3):239–254. doi: 10.1007/BF00508293. [DOI] [PubMed] [Google Scholar]
- Wagner J., Reinhardt D. Characterization of the adrenoceptors mediating the positive ino- and chronotropic effect of phenylephrine on isolated atria from guinea pigs and rabbits by means of adrenolytic drugs. Naunyn Schmiedebergs Arch Pharmacol. 1974;282(3):295–306. doi: 10.1007/BF00501237. [DOI] [PubMed] [Google Scholar]
- Wenzel D. G., Su J. L. Interactions between sympathomimetic amines and blocking agents on the rat ventricle strip. Arch Int Pharmacodyn Ther. 1966 Apr;160(2):379–389. [PubMed] [Google Scholar]
