Differential effects of GABAA receptor antagonists in the control of respiratory neuronal discharge patterns

被引:54
作者
Dogas, Z
Krolo, M
Stuth, EA
Tonkovic-Capin, M
Hopp, FA
McCrimmon, DR
Zuperku, EJ [4 ]
机构
[1] Med Coll Wisconsin, Dept Anesthesiol, Milwaukee, WI 53295 USA
[2] Northwestern Univ, Sch Med, Dept Physiol, Chicago, IL 60611 USA
[3] Northwestern Univ, Sch Med, Inst Neurosci, Chicago, IL 60611 USA
[4] Zablocki Vet Affairs Med Ctr, Res Serv 151, Milwaukee, WI 53295 USA
关键词
D O I
10.1152/jn.1998.80.5.2368
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
To ascertain the role of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) in shaping and controlling the phasic discharge patterns of medullary respiratory premotor neurons, localized pressure applications of the competitive GABA(A) receptor antagonist bicuculline (BIC) and the noncompetitive GABA(A) receptor antagonist picrotoxin (PIC) were studied. Multibarrel micropipettes were used in halothane anesthetized, paralyzed, ventilated, vagotomized dogs to record single unit activity from inspiratory and expiratory neurons in the caudal ventral respiratory group and to picoeject GABA(A) receptor antagonists. The moving time average of phrenic nerve activity was used to determine respiratory phase durations and to synchronize cycle-triggered histograms of discharge patterns. Picoejection of BIC and PIC had qualitatively different effects on the discharge patterns of respiratory neurons. BIC caused an increase in the discharge rate during the neuron's active phase without inducing activity during the neuron's normally silent phase. The resulting discharge patterns were amplified replicas (X2-3) of the underlying preejection phasic patterns. In contrast, picoejection of PIC did not increase the peak discharge rate during the neuron's active phase but induced a tonic level of activity during the neuron's normally silent phase. The maximum effective BIC dose (15 +/- 1.8 pmol/min) was considerably smaller than that for PIC (280 +/- 53 pmol/min). These findings suggest that GABA(A) receptors with differential pharmacology mediate distinct functions within the same neuron, 1) gain modulation that is BIC sensitive but PIC insensitive and 2) silent-phase inhibition blocked by PIG. These studies also suggest that the choice of an antagonist is an important consideration in the determination of GABA receptor function within the respiratory motor control system.
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收藏
页码:2368 / 2377
页数:10
相关论文
共 32 条
[1]
EXPIRATORY BULBOSPINAL NEURONS OF DOGS .1. CONTROL OF DISCHARGE PATTERNS BY PULMONARY STRETCH RECEPTORS [J].
BAJIC, J ;
ZUPERKU, EJ ;
TONKOVICCAPIN, M ;
HOPP, FA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06) :R1075-R1086
[2]
POST-SYNAPTIC INHIBITION OF BULBAR INSPIRATORY NEURONS IN THE CAT [J].
BALLANTYNE, D ;
RICHTER, DW .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 348 (MAR) :67-87
[3]
GABA-A RECEPTOR SUBTYPES - FROM PHARMACOLOGY TO MOLECULAR-BIOLOGY [J].
BURT, DR ;
KAMATCHI, GL .
FASEB JOURNAL, 1991, 5 (14) :2916-2923
[4]
INVOLVEMENT OF AMINO-ACIDS IN PERIODIC INHIBITIONS OF BULBAR RESPIRATORY NEURONS [J].
CHAMPAGNAT, J ;
DENAVITSAUBIE, M ;
MOYANOVA, S ;
RONDOUIN, G .
BRAIN RESEARCH, 1982, 237 (02) :351-365
[5]
CAUDAL MEDULLARY EXPIRATORY NEURON AND INTERNAL INTERCOSTAL NERVE DISCHARGES IN THE CAT - EFFECTS OF LUNG-INFLATION [J].
COHEN, MI ;
FELDMAN, JL ;
SOMMER, D .
JOURNAL OF PHYSIOLOGY-LONDON, 1985, 368 (NOV) :147-178
[6]
EXCITATION AND INHIBITION OF MEDULLARY INSPIRATORY NEURONS BY 2 TYPES OF BURST INSPIRATORY NEURONS IN THE CAT [J].
EZURE, K ;
MANABE, M ;
OTAKE, K .
NEUROSCIENCE LETTERS, 1989, 104 (03) :303-308
[7]
Feldman J L, 1983, Physiologist, V26, P310
[8]
French-Constant R. H., 1993, NATURE, V363, P449
[9]
GURLEY D, 1995, RECEPTOR CHANNEL, V3, P13
[10]
EVIDENCE THAT GLYCINE AND GABA MEDIATE POSTSYNAPTIC INHIBITION OF BULBAR RESPIRATORY NEURONS IN THE CAT [J].
HAJI, A ;
TAKEDA, R ;
REMMERS, JE .
JOURNAL OF APPLIED PHYSIOLOGY, 1992, 73 (06) :2333-2342