Calcium channels coupled to neurotransmitter release at dually innervated neuromuscular junctions in the newborn rat

We studied the effect of several calcium channel blockers (ω-Conotoxin-GVIA, 1 and 3 μM; ω-Agatoxin-IVA, 100 nM; Nitrendipine, 1 and 10 μM) on evoked transmitter release at singly and dually innervated endplates of the levator auris longus muscle from three- to six-day-old rats. In dually innervated...

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Autor principal: Santafé, M.M
Otros Autores: Garcia, N., Lanuza, M.A, Uchitel, O.D, Tomás, J.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2001
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a Calcium Channel Blockers; Calcium Channels; Neurotransmitter Agents; Nitrendipine, 39562-70-4; omega-Agatoxin IVA; omega-Conotoxin GVIA, 92078-76-7 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a NRSCD 
100 1 |a Santafé, M.M 
245 1 0 |a Calcium channels coupled to neurotransmitter release at dually innervated neuromuscular junctions in the newborn rat 
260 |c 2001 
270 1 0 |m Santafé, M.M.; Unitat d'Histologia i Neurobiologia, Facultat Medicina Ciencies Salut, Universitat Rovira i Virgili, carrer St. Llorenç num 21, 43201 Reus, Spain; email: msm@fmcs.urv.es 
506 |2 openaire  |e Política editorial 
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520 3 |a We studied the effect of several calcium channel blockers (ω-Conotoxin-GVIA, 1 and 3 μM; ω-Agatoxin-IVA, 100 nM; Nitrendipine, 1 and 10 μM) on evoked transmitter release at singly and dually innervated endplates of the levator auris longus muscle from three- to six-day-old rats. In dually innervated fibers, a second endplate potential may appear after the first one when we increase the stimulation intensity. The lowest and highest endplate potential amplitudes are designated "small endplate potential" and "large endplate potential", respectively. The percentage of doubly innervated junctions remains almost constant throughout the age range examined. Nevertheless, the percentage of junctions innervated by three or more terminal axons drops, whereas the singly innervated junctions increase. Therefore, between postnatal days 3 and 6, roughly half the neuromuscular junctions may experience the final process of axonal elimination. The synaptic efficacy of the large endplate potential in dual junctions, measured as the mean amplitude of the synaptic potential and mean quantal content, was the same as in the junctions that had become recently mono-innervated in the same postnatal period. In singly innervated fibers, the endplate potential size was strongly reduced by both the P/Q-type voltage-dependent calcium channel blocker ω-Agatoxin-IVA (79.17 ± 4.02%; P < 0.05) and the N-type voltage-dependent calcium channel blocker ω-Conotoxin-GVIA (56.31 ± 7.80%; P < 0.05), whereas endplate potential amplitude was not significantly changed by the L-type voltage-dependent calcium channel blocker Nitrendipine. In dually innervated fibers, the P/Q-type voltage-dependent calcium channel blocker ω-Agatoxin-IVA and L-type voltage-dependent calcium channel blocker Nitrendipine increased the size of the small endplate potential (161.29 ± 47.87% and 109.32 ± 11.03%, respectively; P < 0.05 in both cases) and reduced the large endplate potential (74.42 ± 15.32% and 70.91 ± 10.04%, respectively; P < 0.05 in both cases). The N-type voltage-dependent calcium channel blocker ω-Conotoxin-GVIA significantly increased the small endplate potential in the first few minutes after toxin application (at 10 min: 90.23 ± 17.38%; P < 0.05). This increase was not maintained, while the large endplate potential was strongly inhibited (69.25 ± 7.5%; P < 0.05). In conclusion, in the dually innervated endplates of the newborn rat, presynaptic calcium channel types can have different roles in transmitter release from each of the two inputs, which suggests that nerve terminal voltage-dependent calcium channels are involved in neonatal synaptic maturation. © 2001 IBRO.  |l eng 
536 |a Detalles de la financiación: SAF97-0127 
536 |a Detalles de la financiación: We would like to thank Dr M. R. Fenoll, Dr M. T. Colomina and Lic M. Rosato-Siri for reading the manuscript and offering valuable suggestions. We thank C. Sanmartı́ for technical assistance. This work was supported by grants from the CYCYT (SAF97-0127) and FISS (2000-00/0953). 
593 |a Unitat d'Histologia i Neurobiologia (UHN), Facultat de Medicina i Ciencies de la Salut, Universitat Rovira i Virgili, Carrer St. Llorenc Num 21, 43201 Reus, Spain 
593 |a Laboratorio de Fisiología y Biología Molecular (LFBM), Fac. de Cie. Exact. y Nat., Univ. de Buenos Aires, Cd. Univ., 1428 Buenos Aires, Argentina 
690 1 0 |a Ω-AGATOXIN-IVA 
690 1 0 |a Ω-CONOTOXIN-GVIA 
690 1 0 |a CALCIUM CHANNELS 
690 1 0 |a NITRENDIPINE 
690 1 0 |a RAT 
690 1 0 |a SYNAPSE ELIMINATION 
690 1 0 |a CALCIUM CHANNEL 
690 1 0 |a CALCIUM CHANNEL BLOCKING AGENT 
690 1 0 |a CHOLINERGIC RECEPTOR 
690 1 0 |a NITRENDIPINE 
690 1 0 |a OMEGA AGATOXIN IVA 
690 1 0 |a OMEGA CONOTOXIN GVIA 
690 1 0 |a RINGER SOLUTION 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DRUG EFFECT 
690 1 0 |a ELECTROPHYSIOLOGY 
690 1 0 |a ENDPLATE POTENTIAL 
690 1 0 |a MUSCLE EXCITATION 
690 1 0 |a MUSCLE INNERVATION 
690 1 0 |a NERVE ENDING 
690 1 0 |a NERVE FIBER 
690 1 0 |a NEUROMUSCULAR SYNAPSE 
690 1 0 |a NEUROTRANSMISSION 
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 RAT 
690 1 0 |a AGING 
690 1 0 |a ANIMALS 
690 1 0 |a ANIMALS, NEWBORN 
690 1 0 |a CALCIUM CHANNEL BLOCKERS 
690 1 0 |a CALCIUM CHANNELS 
690 1 0 |a ELECTRIC STIMULATION 
690 1 0 |a EVOKED POTENTIALS 
690 1 0 |a MOTOR ENDPLATE 
690 1 0 |a MUSCLE, SKELETAL 
690 1 0 |a NEUROMUSCULAR JUNCTION 
690 1 0 |a NEUROTRANSMITTER AGENTS 
690 1 0 |a NITRENDIPINE 
690 1 0 |a OMEGA-AGATOXIN IVA 
690 1 0 |a OMEGA-CONOTOXIN GVIA 
690 1 0 |a RATS 
690 1 0 |a RATS, SPRAGUE-DAWLEY 
690 1 0 |a SYNAPSES 
700 1 |a Garcia, N. 
700 1 |a Lanuza, M.A. 
700 1 |a Uchitel, O.D. 
700 1 |a Tomás, J. 
773 0 |d 2001  |g v. 102  |h pp. 697-708  |k n. 3  |p Neuroscience  |x 03064522  |w (AR-BaUEN)CENRE-759  |t Neuroscience 
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