ON THE SIMULTANEOUS ELECTROPHYSIOLOGICAL MEASUREMENTS OF NEUROTRANSMITTER RELEASE AND PERINEURAL CALCIUM CURRENTS FROM FROG MOTOR-NERVE ENDINGS

被引:17
作者
REDMAN, RS
SILINSKY, EM
机构
[1] Department of Molecular Pharmacology and Biological Chemistry, Northwestern University Medical School, Chicago, IL 60611
关键词
NEUROMUSCULAR JUNCTION; ACETYLCHOLINE; CALCIUM CURRENT; NEUROTRANSMITTER RELEASE;
D O I
10.1016/0165-0270(94)00133-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ca2+ currents from the perineural region of motor nerve endings were measured together with evoked acetylcholine (ACh) release (i.e., end-plate potentials EPPs) in frog skeletal muscle in an attempt to define experimental conditions in which simultaneous measurements of both phenomena were feasible. In a solution containing low Ca2+ (0.9 mM), high Mg2+ (10 mM) and modest concentrations of K+ channel blockers (250 mu M tetraethylammonium, 100 mu M 3,4,-diaminopyridine), reliable measurements of perineural Ca2+ currents were possible. For convenience, this solution will be termed 'Ca2+ current' Ringer. The mean number of ACh quanta released in Ca2+ current Ringer was near the midpoint of the relationship between extracellular [Ca2+] and evoked ACh release observed previously in normal Ringer solutions. Consequently, ACh release in response to low-frequency motor nerve stimulation (0.05 Hz) was well maintained, allowing simultaneous measurements of Ca2+ currents and evoked Ach release to be made. Ca2+ currents and EPPs measured simultaneously in Ca2+ current Ringer were increased or decreased in parallel by increasing or decreasing the extracellular Ca2+ concentrations. Ca2+ channel blockers (Cd2+, 500 mu M; omega-conotoxin, 3 mu M) eliminated both EPPs and the Ca2+ component of the perineural current. NaF (10 mM), which stimulates ACh release, produced parallel increases in EPPs and perineural Ca2+ currents. N-G-cyclohexyladenosine (CHA), an A(1) adenosine receptor agonist, inhibits ACh release without effects on perineural currents. The results suggest that the concurrent electrophysiological recording of Ca2+ currents and ACh release in Ca2+ current Ringer is a reliable experimental approach for determining whether drugs or disease states affect Ach release by acting on Ca2+ channels in the presynaptic membrane.
引用
收藏
页码:151 / 159
页数:9
相关论文
共 36 条
[1]   PROTEIN PHOSPHATASE INHIBITOR OKADAIC ACID ENHANCES TRANSMITTER RELEASE AT NEUROMUSCULAR-JUNCTIONS [J].
ABDULGHANI, M ;
KRAVITZ, EA ;
MEIRI, H ;
RAHAMIMOFF, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1803-1807
[2]   EFFECTS OF CHARYBDOTOXIN, A BLOCKER OF CA-2+-ACTIVATED K+ CHANNELS, ON MOTOR-NERVE TERMINALS [J].
ANDERSON, AJ ;
HARVEY, AL ;
ROWAN, EG ;
STRONG, PN .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 95 (04) :1329-1335
[3]   OMEGA-CONOTOXIN DOES NOT BLOCK THE VERAPAMIL-SENSITIVE CALCIUM CHANNELS AT MOUSE MOTOR-NERVE TERMINALS [J].
ANDERSON, AJ ;
HARVEY, AL .
NEUROSCIENCE LETTERS, 1987, 82 (02) :177-180
[4]  
[Anonymous], 1966, NERVE MUSCLE SYNAPSE
[5]   SEPARATION OF 2 PHOSPHORYLASE KINASE PHOSPHATASES FROM RABBIT SKELETAL-MUSCLE [J].
ANTONIW, JF ;
COHEN, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 68 (01) :45-54
[6]   APPARENT BLOCK OF K+ CURRENTS IN MOUSE MOTOR-NERVE TERMINALS BY TETRODOTOXIN, MU-CONOTOXIN AND REDUCED EXTERNAL SODIUM [J].
BRAGA, MFM ;
ANDERSON, AJ ;
HARVEY, AL ;
ROWAN, EG .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 106 (01) :91-94
[7]  
CECCARELLI B, 1980, PHYSIOL REV, V69, P396
[8]   PHARMACOLOGICAL ELEVATION OF CYCLIC-AMP AND TRANSMITTER RELEASE AT THE MOUSE NEUROMUSCULAR-JUNCTION [J].
DRYDEN, WF ;
SINGH, YN ;
GORDON, T ;
LAZARENKO, G .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1988, 66 (03) :207-212
[9]  
GINSBORG BL, 1976, HDB EXPT PHARM, P229
[10]   THE ANTAGONISM BETWEEN BOTULINUM TOXIN AND CALCIUM IN MOTOR-NERVE TERMINALS [J].
GUNDERSEN, CB ;
KATZ, B ;
MILEDI, R .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1982, 216 (1204) :369-376