Browse > Article
http://dx.doi.org/10.11620/IJOB.2013.38.1.013

Four Voltage-Gated Potassium Currents in Trigeminal Root Ganglion Neurons  

Choi, Seung Ho (Dental Science Research Institute, School of Dentistry, Research Center for Biomineralization Disorder, Chonnam National University)
Youn, Chang (Dental Science Research Institute, School of Dentistry, Research Center for Biomineralization Disorder, Chonnam National University)
Park, Ji-Il (Department of Dental Hygiene, Gwangju Health University)
Jeong, Soon-Yeon (Dental Science Research Institute, School of Dentistry, Research Center for Biomineralization Disorder, Chonnam National University)
Oh, Won-Man (Dental Science Research Institute, School of Dentistry, Research Center for Biomineralization Disorder, Chonnam National University)
Jung, Ji-Yeon (Dental Science Research Institute, School of Dentistry, Research Center for Biomineralization Disorder, Chonnam National University)
Kim, Won-Jae (Dental Science Research Institute, School of Dentistry, Research Center for Biomineralization Disorder, Chonnam National University)
Publication Information
International Journal of Oral Biology / v.38, no.1, 2013 , pp. 13-19 More about this Journal
Abstract
Various voltage-gated $K^+$ currents were recently described in dorsal root ganglion (DRG) neurons. However, the characterization and diversity of voltage-gated $K^+$ currents have not been well studied in trigeminal root ganglion (TRG) neurons, which are similar to the DRG neurons in terms of physiological roles and anatomy. This study was aimed to investigate the characteristics and diversity of voltage-gated $K^+$ currents in acutely isolated TRG neurons of rat using whole cell patch clamp techniques. The first type (type I) had a rapid, transient outward current ($I_A$) with the largest current size having a slow inactivation rate and a sustained delayed rectifier outward current ($I_K$) that was small in size having a fast inactivation rate. The $I_A$ currents of this type were mostly blocked by TEA and 4-AP, K channel blockers whereas the $I_K$ current was inhibited by TEA but not by 4-AP. The second type had a large $I_A$ current with a slow inactivation rate and a medium size-sustained delayed $I_K$ current with a slow inactivation rate. In this second type (type II), the sensitivities of the $I_A$ or $I_K$ current by TEA and 4-AP were similar to those of the type I. The third type (type III) had a medium sized $I_A$ current with a fast inactivation rate and a large sustained $I_K$ current with the slow inactivation rate. In type III current, TEA decreased both $I_A$ and $I_K$ but 4-AP only blocked $I_A$ current. The fourth type (type IV) had a smallest $I_A$ with a fast inactivation rate and a large $I_K$ current with a slow inactivation rate. TEA or 4-AP similarly decreased the $I_A$ but the $I_K$ was only blocked by 4-AP. These findings suggest that at least four different voltage-gated $K^+$ currents in biophysical and pharmacological properties exist in the TRG neurons of rats.
Keywords
Trigeminal root ganglion neurons; Voltage-gated $K^+$ currents;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
연도 인용수 순위
1 Gold MS, Shuster MJ, Levine JD. Characterization of six voltage-gated K+ currents in adult rat sensory neurons. J Neurophysiol. 1996;75(6):2629-46.   DOI
2 Liu L, Simon SA. Similarities and differences in the currents activated by capsaicin, piperine, and zingerone in rat trigeminal ganglion cells. J Neurophysiol. 1996;76(3): 1858-69.   DOI
3 Harper AA, Lawson SN. Conduction velocity is related to morphological cell type in rat dorsal root ganglion neurones. The Journal of physiology. 1985;359:31-46.   DOI
4 Harper AA, Lawson SN. Electrical properties of rat dorsal root ganglion neurones with different peripheral nerve conduction velocities. The Journal of physiology. 1985;359: 47-63.   DOI
5 Puil E, Gimbarzevsky B, Miura RM. Quantification of membrane properties of trigeminal root ganglion neurons in guinea pigs. J Neurophysiol. 1986;55(5):995-1016.   DOI
6 Galdzicki Z, Puia G, Sciancalepore M, Moran O. Voltagedependent calcium currents in trigeminal chick neurons. Biochem Biophys Res Commun. 1990;167(3):1015-21.   DOI   ScienceOn
7 Caffrey JM, Eng DL, Black JA, Waxman SG, Kocsis JD. Three types of sodium channels in adult rat dorsal root ganglion neurons. Brain Res. 1992;592(1-2):283-97.   DOI   ScienceOn
8 Akopian AN, Sivilotti L, Wood JN. A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons. Nature. 1996;379(6562):257-62.   DOI   ScienceOn
9 Kim HC, Chung MK. Voltage-dependent sodium and calcium currents in acutely isolated adult rat trigeminal root ganglion neurons. J Neurophysiol. 1999;81(3):1123-34.   DOI
10 Seifert G, Kuprijanova E, Zhou M, Steinhauser C. Developmental changes in the expression of Shaker- and Shabrelated K(+) channels in neurons of the rat trigeminal ganglion. Brain research Molecular brain research. 1999; 74(1-2):55-68.   DOI   ScienceOn
11 Connor JA, Stevens CF. Voltage clamp studies of a transient outward membrane current in gastropod neural somata. The Journal of physiology. 1971;213(1):21-30.   DOI
12 Hermann A, Gorman AL. Effects of 4-aminopyridine on potassium currents in a molluscan neuron. The Journal of general physiology. 1981;78(1):63-86.   DOI   ScienceOn
13 Hermann A, Gorman AL. Effects of tetraethylammonium on potassium currents in a molluscan neurons. The Journal of general physiology. 1981;78(1):87-110.   DOI   ScienceOn
14 Harper AA. Similarities between some properties of the soma and sensory receptors of primary afferent neurones. Experimental physiology. 1991;76(3):369-77.   DOI
15 Devor M, Janig W, Michaelis M. Modulation of activity in dorsal root ganglion neurons by sympathetic activation in nerve-injured rats. J Neurophysiol. 1994;71(1):38-47.   DOI
16 Adams DJ, Oxford GS. Interaction of internal anions with potassium channels of the squid giant axon. The Journal of general physiology. 1983;82(4):429-48.   DOI   ScienceOn
17 Fang Z, Kim JS, Oh SB. Molecular Characterization of Cav2.3 in Rat Trigeminal Ganglion Neurons. International Journal of Oral Biology. 2006; 31:45-51.
18 Kim HJ, Kim HC. Electrophysiological Study on Tetrodotoxin- resistant Sodium Current and its Sensitization by Prostaglandin E_2 in Rat Trigeminal Root Ganglion Neurons. International Journal of Oral Biology. 2002; 27:69-78.
19 Rudy B. Diversity and ubiquity of K channels. Neuroscience. 1988;25(3):729-49.   DOI   ScienceOn
20 Kostyuk PG, Veselovsky NS, Fedulova SA, Tsyndrenko AY. Ionic currents in the somatic membrane of rat dorsal root ganglion neurons-III. Potassium currents. Neuroscience. 1981;6(12):2439-44.   DOI   ScienceOn
21 McFarlane S, Cooper E. Kinetics and voltage dependence of A-type currents on neonatal rat sensory neurons. J Neurophysiol. 1991;66(4):1380-91.   DOI
22 Stansfeld CE, Marsh SJ, Parcej DN, Dolly JO, Brown DA. Mast cell degranulating peptide and dendrotoxin selectively inhibit a fast-activating potassium current and bind to common neuronal proteins. Neuroscience. 1987;23(3):893-902.   DOI   ScienceOn
23 Akins PT, McCleskey EW. Characterization of potassium currents in adult rat sensory neurons and modulation by opioids and cyclic AMP. Neuroscience. 1993;56(3):759-69.   DOI   ScienceOn