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J Physiol Volume 545, Number 1, 119-131, November 15, 2002 DOI: 10.1113/jphysiol.2002.026898
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Journal of Physiology (2002), 545.1, pp. 119-131
© Copyright 2002 The Physiological Society
DOI: 10.1113/jphysiol.2002.026898

Biphasic modulation of synaptic transmission by hypertonicity at the embryonic Drosophila neuromuscular junction

Kazuhiro Suzuki, Tomonori Okamoto and Yoshiaki Kidokoro

Institute for Behavioral Sciences, Gunma University School of Medicine, 3-39-22 Showa-mach, Maebashi 371-8511, Japan

Puff-application of hypertonic saline (sucrose added to external saline) causes a transient increase in the frequency of spontaneous miniature synaptic currents (mSCs) at the neuromuscular junctions of Drosophila embryos. The frequency gradually returns to pre-application levels. External Ca2+ is not needed for this response, but it may modify it. At 50 mM added sucrose, for example, enhanced spontaneous release was observed only in the presence of external Ca2+, suggesting that Ca2+ augments the response. In a high-K+ solution, in which the basal mSC frequency was elevated, higher sucrose concentrations produced an increase in mSC frequency that was followed (during and after the hypertonic exposure) by depression, with the magnitude of both effects increasing with hypertonicity between 100 and 500 mM. Evoked release by nerve stimulation showed only depression in response to hypertonicity. We do not believe that the depression of spontaneous or evoked release can be explained by the depletion of releasable quanta, however, since the frequency of quantal release did not reach levels compatible with this explanation and the enhancement and depression could be obtained independent of one another. In a mutant lacking neuronal synaptobrevin, only the depression of mSC frequency was induced by hypertonicity. Conversely, only the enhancing effect was observed in wild-type embryos when the mSC frequency was elevated with forskolin in Ca2+-free saline. In cultured embryonic Drosophila neurons, Ca2+ signals that were induced by high K+ and detected by Fura-2, were reduced by hypertonicity, suggesting that the depressing response is due to a direct effect of hypertonicity on Ca2+ influx.



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