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The timing of calcium action during neuromuscular transmission
Open accessAbstract
1. When a nerve—muscle preparation is paralysed by tetrodotoxin, brief depolarizing pulses applied to a motor nerve ending cause packets of acetylcholine to be released and evoke end‐plate potentials (e.p.p.s), provided calcium ions are present in the extracellular fluid. 2. By ionophoretic discharge from a 1 M‐CaCl 2 pipette, it is possible to produce a sudden increase in the local calcium concentration at the myoneural junction, at varying times before or after the depolarizing pulse. 3. A brief application of calcium facilitates transmitter release if it occurs immediately before the depolarizing pulse. If the calcium pulse is applied a little later, during the period of the synaptic delay, it is ineffective. 4. It is concluded that the utilization of external calcium ions at the neuromuscular junction is restricted to a brief period which barely outlasts the depolarization of the nerve ending, and which precedes the transmitter release itself. 5. The suppressing effect of magnesium on transmitter release was studied by a similar method, with ionophoretic discharges from a 1 M‐MgCl 2‐filled pipette. The results, though not quite as clear as with calcium, indicate that Mg pulses also are only effective if they precede the depolarizing pulses.
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Cited by
Wightman, R. M., Jankowski, J. A., Kennedy, R. T., Kawagoe, K. T., Schroeder, T. J., Leszczyszyn, D. J., Near, J. A., Diliberto, E. J., & Viveros, O. H. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.23.10754 · Cited by 893
Miller, S. (1986) · Cell · doi:10.1016/0092-8674(86)90008-5 · Cited by 864
Synaptotagmin I Functions as a Calcium Sensor to Synchronize Neurotransmitter Release
Yoshihara, M., & Littleton, J. T. (2002) · Neuron · doi:10.1016/s0896-6273(02)01065-6 · Cited by 285
Routh, V. H. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00761-8 · Cited by 237
Distinct Initial SNARE Configurations Underlying the Diversity of Exocytosis
Kasai, H., Takahashi, N., & Tokumaru, H. (2012) · Physiological Reviews · doi:10.1152/physrev.00007.2012 · Cited by 150
Approaches and Limitations in the Investigation of Synaptic Transmission and Plasticity
Glasgow, S. D., McPhedrain, R., Madranges, J. F., Kennedy, T. E., & Ruthazer, E. S. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00020 · Cited by 100
Conserved Prefusion Protein Assembly in Regulated Exocytosis
Rickman, C., Jiménez, J. L., Graham, M. E., Archer, D. A., Soloviev, M., Burgoyne, R. D., & Davletov, B. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-07-0620 · Cited by 74
Yoshihara, M., & Yoshihara, M. (2018) · Journal of Neurogenetics · doi:10.1080/01677063.2018.1468443 · Cited by 40
Bradberry, M. M., Bao, H., Lou, X., & Chapman, E. R. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.007929 · Cited by 38
Molecular Mechanism of Active Zone Organization at Vertebrate Neuromuscular Junctions
Nishimune, H. (2012) · Molecular Neurobiology · doi:10.1007/s12035-011-8216-y · Cited by 29
“synaptic vesicles to the presynaptic membrane [68–74], and active zones are synaptic vesicle release sites [12, 13].”
Background
Metadata
- Authors
- Katz, B., & Miledi, R.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 1967-04
- Volume
- 189
- Issue
- 3
- Pages
- 535-544
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- OpenAlex
- W2040477003
- Cited by
- 561
- References
- 0
- FWCI
- 4.91
- Type
- journal article
- Language
- en
- Open access
- green
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