Decrements in per pulse release of norepinephrine, antagonist potentiation of release and presynaptic receptor theory

被引:0
作者
Kalsner, S [1 ]
Abdali, SA [1 ]
机构
[1] CUNY City Coll, Sch Med, Dept Physiol & Pharmacol, New York, NY 10031 USA
关键词
presynaptic receptors; negative feedback; transmitter release; norepinephrine;
D O I
10.1016/S0361-9230(03)00115-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In recent decades the theory that amine transmitter release at nerve terminals is routinely regulated through negative feedback systems sensing and responding to the instantaneous perineuronal concentration of previously liberated transmitter has assumed pre-eminence. However, observations indicate a major drop off in per pulse transmitter release when only two or four stimulation pulses are administered, reflecting the unexpectedly prompt operation of feedback inhibition. We explored this quandary in our understanding of control of transmitter release by axonal depolarization versus terminal feedback using isotopic norepinephrine and in vitro slices of rabbit hippocampus. A technique of continuous collection of superfusate over a 30 min cycle of stimulation utilizing a wide range of intervals between individual stimulation pulses was used. Following simulation with single pulses even 60 s apart or pseudo one pulses 150 s apart a marked decline in per pulse release was noted. The deficits in per pulse release were not related to the number of pulse delivered at any time over the course of a 30 min stimulation period. The pulse decrements were independent of the activity of neuronal uptake and of superfusion flow rate or even individual pulse duration and frequency. Presynaptic receptor antagonists, potentiated efflux near maximally with the second of only two pulses. Potentiations were independent of pulse number, pulse duration, or frequency. No linkage between perineuronal transmitter concentrations and the antagonist potentiation of release was found. However, the decrements in per pulse release with multiple pulses and the potentiation by alpha presynaptic antagonists occurred under the same test conditions. We conclude that the pulse deficit can be looked at as largely attributable to an enhanced efflux with delivery of the first pulse in a train of pulses, rather then to a pattern of progressively declining efflux linked to increasing extracellular transmitter levels as frequency and pulse number increase. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:173 / 182
页数:10
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