Browse > Article

The effect of extracellular Mg2+ on action potential in guinea pig papillary muscles  

Chang, Sung-Eun (Bio-Safety Research Institute, Chonbuk National University)
Kim, Shang-Jin (Bio-Safety Research Institute, Chonbuk National University)
Kang, Hyung-Sub (Bio-Safety Research Institute, Chonbuk National University)
Kim, Jin-Shang (Bio-Safety Research Institute, Chonbuk National University)
Publication Information
Korean Journal of Veterinary Research / v.43, no.1, 2003 , pp. 31-39 More about this Journal
Abstract
We have investigated the effect of extracellular $Mg^{2+}$ ($[Mg^2+]_o$) on action potential duration (APD) in guinea pig papillary muscles by using microelectrodes. Increasing $[Mg^2+]_o$ resulted in progressive negative inotropic effect, progressive ascending depolarization of membrane potential, and increase in intracellular $Mg^{2+}$ concentration. In addition, increase in $[Mg^2+]_o$ from 1.1 to 3, 6, 10, and 20 mM produced a reversible dose-dependent shortening of both APD at 30% ($APD_{30}$) and 90% repolarization ($APD_{90}$), especially showing a tendency towards more remarkable prominent shortening in $APD_{30}$ than $APD_{90}$. Cooling from 37 to 33 and $27^{\circ}C$ diminished the $[Mg^2+]_o$-induced APD shortening. Increase in extracellular $Ca^{2+}$ concentration from 1.8 to 3.6 and 5.4 mM caused a significant depressed effect on the increasing $[Mg^2+]_o$-induced APD shortening. Furthermore, increase in $[Mg^2+]_o$ from 1.1 to 10 and 20 mM produced a significant depressed effect on the APD shortening induced by extracellular $Ca^{2+}$. Pretreatment of verapamil and imipramine significantly attenuated the increasing $[Mg^2+]_o$-induced APD shortening in both $APD_{30}$ and $APD_{90}$, whereas the $[Mg^2+]_o$-induced APD shortening was not affected by strophanthidin, glibenclamide and tetrabutylammonium. These findings suggest that the effects of $[Mg^2+]_o$ on APD are probably due to a decrease in ionic transport across plasma membrane. In conclusion, the present study indicates that $[Mg^2+]_o$ exerts antiarrhythmic activities by antagonistic actions on intracellular $Ca^{2+}$.
Keywords
magnesium; calcium; action potential duration; temperature; intracellular $Mg^{2+}$;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Shine KI. Myocardial effects of magnesium. Am J Physiol, 237:H413-H423, 1979
2 Rasmussen HS, McNair P, Nwregard P, et at. Intravenous magnesium in acute myocardial infaction. Lancet, 8475:234-236, 1986
3 Aomine M, Tatsukawa Y, Yamato T, et al. Anti-arrhythmic effects of magnesium on rat papillary muscls and guinea pig ventricular myocytes. Gen Pharmac, 32:107-114, 1999
4 Zhang S, Sawanobori T, Adaniya H, et at. Dual effects of external magnesium on action potential duration in guinea pig ventricular myocytes. Am J Physiol, 268:H2321-2328, 1995
5 Smith LF, Heagerty AM, Bing RF, et al. Intravenous infusion of magnesium sulphate acute myocardial infarction, effects on arrhythmias and mortality. Int J Cardiol, 12:175-180, 1986
6 Tso EL, Barish RA. Magnesium: clinical considerations. J Emerg Med. 10:735-745, 1992
7 Shibata EF, Giles WR. lonic currents that generate the spontaneous diastolic depolarization in individual cardiac pacemaker cells. Proc Natl Acad Sci USA. 82:7796-800, 1985
8 Siegelbaum SA, Tsien RW. Calcium-activated transient outward current in calf cardiac Purkinje fibres. J Physiol, 299:485-506, 1980
9 Watanahe Y, Dreifus LS. Electrophysiological effects of magnesium and its interactions with potassium. Car-diovasc Res, 6:79-88, 1972
10 White RE, Hartzell HC. Effects of intracellular free magnesium on calcium current in isolated cardiac myocytes. Science, 239:778-780, 1988
11 Wu JY, Lipsius SL. Effects of extracellular $Mg^{2+}$ on T- and L-type $Ca^{2+}$ cunents in single atrial niyocytes. Am J Physiol, 259:H1842-1850, 1990
12 Keren A, Tzivoni D. Magnesium therapy in ventricular arrhythmias. PACE, 13:937-945, 1990
13 Ingemansson MP, Arlock P, Olsson SB. Effects of magnesium and glucose, insulin, patassium(GIK) solution on the action potential parameters of guinea-pig atrial muscle. Acta PhysioI Scand, 164:173-179, 1998
14 Rude R, Manoogian C, Ehrlich L, et at. Mechanisms of blood pressure regulation by magnesium in man. Magnesium, 8:266-273, 1989
15 Simmons MA, Hartzell HC. A quantitative analysis of the acetylcholine-activated potassium current in single cells from frog atrium. Pflygers Arch, 409:454-461, 1987
16 Matsuda H, Saigusa A, Irisawa H. OhMic conductance through the inwardly rectifying K channel and blocking by internal $Mg^{2+}$. Nature. 325:156-159, 1987
17 Takanaka C, Ogunyankin KO, Sarma JS, et aI. Antiarrhythmic and arrhythmpgenic actions of varying levels of extracellular magnesiurn: possible cellular basis for the differences m the eHScacy of magnesium and lidocaine in torsade de pointes. J Cardiovasc Pharmacol Ther, 2:125-134, 1997
18 Agus ZS, Morad M Modulation of cardiac ion channels by magnesium. Annu Rev Physrol, 53:299-307, 1991
19 Redwood SR, Taggart PI, Sutton PM, et aI. Effect of magnesium on the monophasic action potential during early ischemia in the in vivo human heart. J Am Coll Cardiol, 28:1765-1769, 1996
20 Parikka HJ, Toivonen LK. Acute effects of intravenous magnesium on ventricular refractoriness and monophasic action potential duration in humans. Scand Cardiovasc J, 33:300-305, 1999
21 Hall SK, Fry CH. Magnesium affects excition, con-duction, and contraction of isolated mammalian cardiac muscle. Am J Physiol, 263:H622-633, 1992
22 Dichtl A, Vierling W. Inhibition by magnesium of calcium inward current in heart ventricular muscle. Eur J Phanmcol., 204:243-248, 1991
23 Howarth FC, Waring J, Hustler BI, et at. Effects of extracellular magnesium and beta adrenergic stimulation on contractile force and magnesium mobilization in the isolated rat heart. Magnes Res, 7: 187-197, 1994
24 Satoh Y, Sugiyama A, Tamura K, et at. Effect of magnesium sulfate 0n the haloperidol-induced QT pio-longation assessed in the canine in vivo model under the monitoring of monophasic action potantial. Jpn Circ J, 64:445-451, 2000
25 White RE, Haatzell HC. Magnesium ions in caidiac function: Begulator of icn channels and second messengeis. Biochem Pharmacol, 38:859-867, 1989
26 Noble D. The surprising heart: A review of recent progress in cardiac electrophysiology. J PhysioI(Lond), 353:1-50, 1984
27 Lloyd T, Iseri MD, James H, et al. Magnesium: nature's physiologic calcium blocker. Am Heart J, 108:188-193, 1984
28 Horie M, Irisawa H, Noma A. Voltage-dependent mag-nesium block of adenosine-triphosphate-seositive po-tassium channel in guinea-pig ventricular cells. J PhysioI, 387:251-272, 1987
29 Hahin R, Campbell DT. Simple shifts in the voltage dependence of sodium channel gating caused by divalent cations. J Gen PhysioI, 82:785-805, 1983
30 Kirkels JH, van Echteld CJA, Ruigrok TJC. Intracellular magnesium during myocardial ischemia and reperfusion: possible consequences for postischemic recovery. J MoI Cell Cardiol. 21:1209-1218, 1989
31 Aceto E, Vassalle M Magnesium and intracellular sodium activity in cardiac purkinje fibers. Magnes Trace Elem, 9:152-162, 1990
32 Laurant P, Dalle M, Berthelot A, et at. TIme-course of the change in blood pressure level in magnesium-deficient Wistar rats. Br J Nutr, 82:243-251, 1999
33 Murasato Y, Harada Y, Ikeda M, et al. Effect of magnesium deficiency on autonomic circulatory regu-lation in ocnscious rats. Hypertension, 34:247-252, 1999
34 Shatokk MJ, Hearse DJ, Fry CH. The ionic basis of the antiischemic properties of magnesium in the heart. J Am Coll Nutr, 6:27-33, 1987