Nifedipine-mediated mobilization of intracellular calcium stores increases spontaneous neurotransmitter release at neonatal rat motor nerve terminals

The modulation of spontaneous release of acetylcholine by specific Ca2+ channel blockers was studied at neonatal rat neuromuscular junction. During early postnatal periods (0-4 days), blockers of N- and P/Q-type Ca2+ channels did not affect miniature endplate potential (MEPP) frequency. Unexpectedly...

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Autor principal: Piriz, J.
Otros Autores: Siri, M.D.R, Pagani, R., Uchitel, O.D
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2003
Acceso en línea:Registro en Scopus
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024 7 |2 scopus  |a 2-s2.0-0037960952 
024 7 |2 cas  |a calciseptine, 134710-25-1; calcium ion, 14127-61-8; isradipine, 75695-93-1, 88977-22-4; nifedipine, 21829-25-4; nitrendipine, 39562-70-4; ryanodine, 15662-33-6; thapsigargin, 67526-95-8; Calcium Channel Blockers; Calcium, 7440-70-2; Neurotransmitter Agents; Nifedipine, 21829-25-4 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JPETA 
100 1 |a Piriz, J. 
245 1 0 |a Nifedipine-mediated mobilization of intracellular calcium stores increases spontaneous neurotransmitter release at neonatal rat motor nerve terminals 
260 |c 2003 
270 1 0 |m Uchitel, O.D.; Lab. de Fisiol. y Biologia Molecular, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Buenos Aires 1428, Argentina; email: odu@fibertel.com.ar 
506 |2 openaire  |e Política editorial 
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504 |a Emptage, N.J., Reid, C.A., Fine, A., Calcium stores in hippocampal synaptic boutons mediate short-term plasticity, store-operated Ca2+ entry and spontaneous transmitter release (2001) Neuron, 29, pp. 197-208 
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504 |a Flink, M.T., Atchison, W.D., Iberiotoxin-induced block of KCa channels induces dihydropyridine sensitivity of ACh release from mammalian motor nerve terminals (2003) J Pharmacol Exp Ther, 305, pp. 646-652 
504 |a Hirasawa, M., Pittman, Q.J., Nifedipine facilitates neurotransmitter release independently of calcium channels (2003) Proc Natl Acad Sci USA, 100, pp. 6139-6144 
504 |a Hubbard, J.I., Jones, S.F., Landau, E.M., On the mechanism by which calcium and magnesium affect the spontaneous release of transmitter from mammalian motor nerve terminals (1968) J Physiol (Lond), 194, pp. 355-380 
504 |a Katz, E., Protti, D.A., Ferro, P.A., Rosato Siri, M.D., Uchitel, O.D., Effects of Ca2+ channel blocker neurotoxins on transmitter release and presynaptic currents at the mouse neuromuscular junction (1997) Br J Pharmacol, 121, pp. 1531-1540 
504 |a Krizaj, D., Bao, J.X., Schmitz, Y., Witkovsky, P., Copenhagen, D.R., Caffeine-sensitive calcium stores regulate synaptic transmission from retinal rod photoreceptors (1999) J Neurosci, 19, pp. 7249-7261 
504 |a Llano, I., Gonzalez, J., Caputo, C., Lai, F.A., Blayney, L.M., Tan, Y.P., Marty, A., Presynaptic calcium stores underlie large-amplitude miniature IPSCs and spontaneous calcium transients (2000) Nat Neurosci, 3, pp. 1256-1265 
504 |a Losavio, A., Muchnik, S., Spontaneous acetylcholine release in mammalian neuromuscular junctions (1997) Am J Physiol, 273, pp. C1835-C1841 
504 |a Majeed, I.A., Murray, W.J., Newton, D.W., Othman, S., Al-Turk, W.A., Spectrophotometric study of the photodecomposition kinetics of nifedipine (1987) J Pharm Pharmacol, 39, pp. 1044-1046 
504 |a Narita, K., Akita, T., Osanai, M., Shirasaki, T., Kijima, H., Kuba, K., A Ca2+-induced Ca2+ release mechanism involved in asynchronous exocytosis at frog motor nerve terminals (1998) J Gen Physiol, 112, pp. 593-609 
504 |a Neher, E., Vesicle pools and Ca2+ microdomains: New tools for understanding their roles in neurotransmitter release (1998) Neuron, 20, pp. 389-399 
504 |a Pancrazio, J.J., Viglione, M.P., Kim, Y.I., Effects of Bay K 8644 on spontaneous and evoked transmitter release at the mouse neuromuscular junction (1989) Neuroscience, 30, pp. 215-221 
504 |a Protti, D.A., Szczupak, L., Scornik, F.S., Uchitel, O.D., Effect of α-conotoxin GVIA on neurotransmitter release at the mouse neuromuscular junction (1991) Brain Res, 557, pp. 336-339 
504 |a Protti, D.A., Uchitel, O.D., Transmitter release and presynaptic Ca2+ currents blocked by the spider toxin omega-Aga-IVA (1993) Neuroreport, 5, pp. 333-336 
504 |a Rahamimoff, R., Alnaes, E., Inhibitory action of ruthenium red on neuromuscular transmission (1973) Proc Natl Acad Sci USA, 70, pp. 3413-3416 
504 |a Redfern, P.A., Neuromuscular transmission in new-born rats (1970) J Physiol (Lond), 209, pp. 701-709 
504 |a Rosato Siri, M.D., Uchitel, O.D., Calcium channels coupled to neurotransmitter release at neonatal rat neuromuscular junctions (1999) J Physiol (Lond), 514, pp. 533-540 
504 |a Scholze, A., Plant, T.D., Dolphin, A.C., Nurnberg, B., Functional expression and characterization of a voltage-gated CaV1.3 (α1D) calcium channel subunit from an insulin-secreting cell line (2001) Mol Endocrinol, 15, pp. 1211-1221 
504 |a Sugiura, Y., Ko, C.P., Novel modulatory effect of L-type calcium channels at newly formed neuromuscular junctions (1997) J Neurosci, 17, pp. 1101-1111 
504 |a Triggle, D.J., The 1,4-dihydropyridine nucleus: A pharmacophoric template part 1. Actions at ion channels (2003) Mini Rev Med Chem, 3, pp. 217-225 
504 |a Uchitel, O.D., Toxins affecting calcium channels in neurons (1997) Toxicon, 35, pp. 1161-1191 
504 |a Uchitel, O.D., Protti, D.A., Sanchez, V., Cherksey, B.D., Sugimori, M., Llinas, R., P-type voltage-dependent calcium channel mediates presynaptic calcium influx and transmitter release in mammalian synapses (1992) Proc Natl Acad Sci USA, 89, pp. 3330-3333 
504 |a Urbano, F.J., Uchitel, O.D., L-Type calcium channels unmasked by cell-permeant Ca2+ buffer at mouse motor nerve terminals (1999) Pfluegers Arch, 437, pp. 523-528 
504 |a Weigl, L.G., Hohenegger, M., Kress, H.G., Dihydropyridine-induced Ca2+ release from ryanodine-sensitive Ca2+ pools in human skeletal muscle cells (2000) J Physiol (Lond), 525, pp. 461-469 
504 |a Yasuda, O., Morimoto, S., Chen, Y., Jiang, B., Kimura, T., Sakakibara, S., Koh, E., Ogihara, T., Calciseptine binding to a 1,4-dihydropyridine recognition site of the L-type calcium channel of rat synaptosomal membranes (1993) Biochem Biophys Res Commun, 194, pp. 587-594 
520 3 |a The modulation of spontaneous release of acetylcholine by specific Ca2+ channel blockers was studied at neonatal rat neuromuscular junction. During early postnatal periods (0-4 days), blockers of N- and P/Q-type Ca2+ channels did not affect miniature endplate potential (MEPP) frequency. Unexpectedly, treatment with the L-type Ca2+ channel antagonist nifedipine, although not when treated with isradipine, nitrendipine, or calciseptine, resulted in strong increase in MEPP frequency. The potentiation effect of nifedipine was dose-dependent with a 56-fold maximum effect with 15 μM. The effect decreased during the first two postnatal weeks and disappeared by the third. The effect of nifedipine was not dependent on extracellular Ca2+ and was not altered by the presence of other Ca2+ channel blockers. In contrast, it was abolished by depleting intracellular Ca2+ stores with μM thapsigargin and was partially inhibited by 10 μM ryanodine. In conclusion, we report a new ryanodine receptor-mediated effect of nifedipine on neonatal neuromuscular junction that may indicate the developmental expression of a specific receptor channel that interacts with intracellular Ca2+ stores. This effect of nifedipine should also be considered when using this drug as either atherapeutic or a research tool.  |l eng 
593 |a Depto. Fisiol. Biol. Cel. Molec., Instituto de Fisiología, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Instituto Cajal, Consejo Sup. de Invest. Cientificas, Avenida Doctor Arce 37, 28002 Madrid, Spain 
593 |a Biophysics Sector, Ist. Naz. di Fis. della Materia Unit, Intl. School for Advanced Studies, Via Beirut 2-4 (34014), Trieste, Italy 
593 |a Lab. de Fisiol. y Biologia Molecular, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Buenos Aires 1428, Argentina 
690 1 0 |a CALCISEPTINE 
690 1 0 |a CALCIUM CHANNEL BLOCKING AGENT 
690 1 0 |a CALCIUM CHANNEL L TYPE 
690 1 0 |a CALCIUM ION 
690 1 0 |a ISRADIPINE 
690 1 0 |a NEUROTRANSMITTER 
690 1 0 |a NIFEDIPINE 
690 1 0 |a NITRENDIPINE 
690 1 0 |a OMEGA AGATOXIN VIA 
690 1 0 |a RYANODINE 
690 1 0 |a RYANODINE RECEPTOR 
690 1 0 |a THAPSIGARGIN 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a CALCIUM CELL LEVEL 
690 1 0 |a CALCIUM TRANSPORT 
690 1 0 |a CONCENTRATION RESPONSE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DIAGNOSTIC VALUE 
690 1 0 |a DRUG EFFECT 
690 1 0 |a DRUG MECHANISM 
690 1 0 |a DRUG USE 
690 1 0 |a LONG TERM POTENTIATION 
690 1 0 |a MINIATURE ENDPLATE POTENTIAL 
690 1 0 |a NERVE ENDING 
690 1 0 |a NEUROMUSCULAR SYNAPSE 
690 1 0 |a NEUROTRANSMITTER RELEASE 
690 1 0 |a NEWBORN 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a RAT 
690 1 0 |a TIME SERIES ANALYSIS 
690 1 0 |a AGE FACTORS 
690 1 0 |a ANIMALS 
690 1 0 |a CALCIUM 
690 1 0 |a CALCIUM CHANNEL BLOCKERS 
690 1 0 |a ELECTROPHYSIOLOGY 
690 1 0 |a INTRACELLULAR FLUID 
690 1 0 |a MOTOR ENDPLATE 
690 1 0 |a MOTOR NEURONS 
690 1 0 |a NEUROTRANSMITTER AGENTS 
690 1 0 |a NIFEDIPINE 
690 1 0 |a RATS 
690 1 0 |a RATS, SPRAGUE-DAWLEY 
700 1 |a Siri, M.D.R. 
700 1 |a Pagani, R. 
700 1 |a Uchitel, O.D. 
773 0 |d 2003  |g v. 306  |h pp. 658-663  |k n. 2  |p J. Pharmacol. Exp. Ther.  |x 00223565  |w (AR-BaUEN)CENRE-825  |t Journal of Pharmacology and Experimental Therapeutics 
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