{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,4]],"date-time":"2026-06-04T14:32:43Z","timestamp":1780583563124,"version":"3.54.1"},"reference-count":57,"publisher":"American Physiological Society","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurophysiology"],"published-print":{"date-parts":[[1998,4,1]]},"abstract":"<jats:p>Schwartz, Neil E. and Simon Alford. Modulation of pre- and postsynaptic calcium dynamics by ionotropic glutamate receptors at a plastic synapse. J. Neurophysiol. 79: 2191\u20132203, 1998. This study was conducted to assess the role of ionotropic glutamate receptors in the modulation of calcium dynamics on both sides of a vertebrate plastic synapse. Retrograde labeling of neuronal elements with high-affinity calcium-sensitive dyes was used in conjunction with confocal imaging techniques in an in vitro lamprey brain stem preparation. A prolonged calcium transient was measured both pre- and postsynaptically in response to a period of high-frequency (\u201ctetanic\u201d) stimulation to the vestibulospinal-reticulospinal synapse. The ionotropic glutamate receptor antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (10 \u03bcM) and d,l\u22122-amino-5-phosphonopentanoate (d,l-AP5; 100 \u03bcM) reduced the calcium signal in both compartments of the synapse. The presynaptic d,l-AP5\u2013sensitive component was enhanced markedly by the removal of Mg<jats:sup>2+<\/jats:sup>from the superfusate. Increasing the extracellular stimulus intensity progressively augmented the presynaptic calcium signal, suggesting the recruitment of excitatory axo-axonic inputs onto these fibers. Further, the presence of an excitatory amino acid-mediated presynaptic potential underlying a component of the Ca<jats:sup>2+<\/jats:sup>signal was demonstrated by electrophysiological recordings from vestibulospinal axons. Bath application of agonist, in the presence of tetrodotoxin (1 \u03bcM), confirmed the existence of N-methyl-d-aspartate receptors at the presynaptic element capable of modulating calcium levels. The postsynaptic Ca<jats:sup>2+<\/jats:sup>response, which is known to be necessary for long-term potentiation (LTP) induction at this synapse, was localized to areas of the dendritic tree that correlated with the location of known synaptic inputs; thus the synaptically activated rise in postsynaptic calcium may confer the synapse specificity of LTP induction previously demonstrated. In summary, we have demonstrated the existence of physiologically activated presynaptic ionotropic glutamate receptors that are capable of modulating levels of intracellular calcium and have highlighted the importance of receptor-mediated increases in postsynaptic calcium for neuronal plasticity in the lamprey.<\/jats:p>","DOI":"10.1152\/jn.1998.79.4.2191","type":"journal-article","created":{"date-parts":[[2017,12,25]],"date-time":"2017-12-25T07:39:54Z","timestamp":1514187594000},"page":"2191-2203","source":"Crossref","is-referenced-by-count":11,"title":["Modulation of Pre- and Postsynaptic Calcium Dynamics by Ionotropic Glutamate Receptors at a Plastic Synapse"],"prefix":"10.1152","volume":"79","author":[{"given":"Neil E.","family":"Schwartz","sequence":"first","affiliation":[{"name":"Department of Physiology and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Simon","family":"Alford","sequence":"additional","affiliation":[{"name":"Department of Physiology and"},{"name":"Northwestern University Institute for Neuroscience, Northwestern University Medical School, Chicago, Illinois 60611"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"24","reference":[{"key":"B1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-8993(93)91370-8"},{"key":"B2","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.1993.sp019838"},{"key":"B3","doi-asserted-by":"publisher","DOI":"10.1016\/0006-8993(90)91266-J"},{"key":"B4","doi-asserted-by":"publisher","DOI":"10.1523\/JNEUROSCI.15-11-07528.1995"},{"key":"B5","doi-asserted-by":"publisher","DOI":"10.1111\/j.1749-6632.1991.tb36505.x"},{"key":"B6","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.1992.sp019126"},{"key":"B7","doi-asserted-by":"publisher","DOI":"10.1016\/0896-6273(95)90237-6"},{"key":"B8","doi-asserted-by":"publisher","DOI":"10.1111\/j.1476-5381.1994.tb16902.x"},{"key":"B9","doi-asserted-by":"publisher","DOI":"10.1038\/346724a0"},{"key":"B10","doi-asserted-by":"publisher","DOI":"10.1038\/361031a0"},{"key":"B11","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.1973.sp010273"},{"key":"B12","doi-asserted-by":"publisher","DOI":"10.1016\/0006-8993(87)90397-0"},{"key":"B13","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.1997.sp021940"},{"key":"B14","doi-asserted-by":"publisher","DOI":"10.1113\/jphysiol.1983.sp014478"},{"key":"B15","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1016\/S0031-6997(25)00025-0","volume":"41","author":"Collingridge G. 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