The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Synaptic Control of Motoneuronal Excitability
Open accessAbstract
Movement, the fundamental component of behavior and the principal extrinsic action of the brain, is produced when skeletal muscles contract and relax in response to patterns of action potentials generated by motoneurons. The processes that determine the firing behavior of motoneurons are therefore important in understanding the transformation of neural activity to motor behavior. Here, we review recent studies on the control of motoneuronal excitability, focusing on synaptic and cellular properties. We first present a background description of motoneurons: their development, anatomical organization, and membrane properties, both passive and active. We then describe the general anatomical organization of synaptic input to motoneurons, followed by a description of the major transmitter systems that affect motoneuronal excitability, including ligands, receptor distribution, pre- and postsynaptic actions, signal transduction, and functional role. Glutamate is the main excitatory, and GABA and glycine are the main inhibitory transmitters acting through ionotropic receptors. These amino acids signal the principal motor commands from peripheral, spinal, and supraspinal structures. Amines, such as serotonin and norepinephrine, and neuropeptides, as well as the glutamate and GABA acting at metabotropic receptors, modulate motoneuronal excitability through pre- and postsynaptic actions. Acting principally via second messenger systems, their actions converge on common effectors, e.g., leak K+current, cationic inward current, hyperpolarization-activated inward current, Ca 2+channels, or presynaptic release processes. Together, these numerous inputs mediate and modify incoming motor commands, ultimately generating the coordinated firing patterns that underlie muscle contractions during motor behavior.
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Cites
The Integrative Action of the Nervous System.
Sherrington, C. (1907) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-190734120-00021 · Cited by 4,136
The Glutamate Receptor Ion Channels
Dingledine, R., Borges, K., Bowie, D., & Traynelis, S. F. (1999) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01394-2 · Cited by 3,554
Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 3,535
Steinbusch, H. W. M. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90146-9 · Cited by 2,415
Macdonald, R. L., & Olsen, R. W. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.003033 · Cited by 1,975
Swanson, L. W., & Kuypers, H. G. J. M. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901940306 · Cited by 1,413
Changing subunit composition of heteromeric NMDA receptors during development of rat cortex
Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N., & Jan, L. Y. (1994) · Nature · doi:10.1038/368144a0 · Cited by 1,377
Shigemoto, R., Kinoshita, A., Wada, E., Nomura, S., Ohishi, H., Takada, M., Flor, P. J., Neki, A., Abe, T., Nakanishi, S., et al. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07503.1997 · Cited by 1,116
A family of metabotropic glutamate receptors
Tanabe, Y., Masu, M., Ishii, T., Shigemoto, R., & Nakanishi, S. (1992) · Neuron · doi:10.1016/0896-6273(92)90118-w · Cited by 940
Baude, A., Nusser, Z., Roberts, J. D. B., Mulvihill, E., Jeffrey Mcllhinney, R. A., & Somogyi, P. (1993) · Neuron · doi:10.1016/0896-6273(93)90086-7 · Cited by 927
Jones, B. E., & Yang, T. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902420105 · Cited by 896
The Tetrameric Structure of a Glutamate Receptor Channel
Rosenmund, C., Stern-Bach, Y., & Stevens, C. F. (1998) · Science · doi:10.1126/science.280.5369.1596 · Cited by 794
Control of Kinetic Properties of AMPA Receptor Channels by Nuclear RNA Editing
Lomeli, H., Mosbacher, J., Melcher, T., Höger, T., Geiger, J. R. P., Kuner, T., Monyer, H., Higuchi, M., Bach, A., & Seeburg, P. H. (1994) · Science · doi:10.1126/science.7992055 · Cited by 746
Adenosine, Adenosine Receptors and the Actions of Caffeine
Fredholm, B. B. (1995) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.1995.tb00111.x · Cited by 597
Vasopressin and oxytocin receptors in the central nervous system
Tribollet, E., & Barberis, C. (1996) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v10.i1.60 · Cited by 399 · cited 2×
“The V1 and oxytocin receptors interact via Gaq/11 to activate PLC and downstream signaling cascades in vascular smooth muscle, corticotropes, and neurons (56, 57, 974); whether this signaling pathway contributes to effects of AVP and oxytocin on motoneurons remains to be determined.”
BackgroundGereau, R., & Conn, P. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06879.1995 · Cited by 352
Swanson, L. W., & McKellar, S. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901880108 · Cited by 336
The role of NMDA receptors in information processing
Daw, N. W., Stein, P. S. G., & Fox, K. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.001231 · Cited by 311 · cited 2×
“In addition, their long-duration excitatory postsynaptic currents (EPSC), Ca(21) permeability, and voltage dependence are important in the detection and reinforcement of weakly correlated synaptic inputs that is thought to contribute to use-dependent synaptic plasticity during development, as well in the adult (279, 8…”
BackgroundWang, Z., & McCormick, D. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-05-02199.1993 · Cited by 307
Tribollet, E., Charpak, S., Schmidt, A., Dubois-Dauphin, M., & Dreifuss, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-05-01764.1989 · Cited by 228
Spike-frequency adaptation studied in hypoglossal motoneurons of the rat
Sawczuk, A., Powers, R. K., & Binder, M. D. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.5.1799 · Cited by 144
Molecular evidence for early activity-dependent development of hamster motor neurons
Kalb, R., & Hockfield, S. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-07-02350.1988 · Cited by 102
Winzer-Serhan, U. H., Raymon, H. K., Broide, R. S., Chen, Y., & Leslie, F. M. (1996) · Neuroscience · doi:10.1016/s0306-4522(96)00369-7 · Cited by 96
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Application of a translational profiling approach for the comparative analysis of CNS cell types
Doyle, J. P., Dougherty, J. D., Heiman, M., Schmidt, E. F., Stevens, T. R., Ma, G., Bupp, S., Shrestha, P., Shah, R. D., Doughty, M. L., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.029 · Cited by 912
Skeletal muscle performance and ageing
Tieland, M., Trouwborst, I., & Clark, B. C. (2018) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12238 · Cited by 904
Del Negro, C. A., Funk, G. D., & Feldman, J. L. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0003-6 · Cited by 663
Self-citationShunting Inhibition Modulates Neuronal Gain during Synaptic Excitation
Mitchell, S. J., & Silver, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00200-9 · Cited by 602
CNS Distribution of Members of the Two-Pore-Domain (KCNK) Potassium Channel Family
Talley, E. M., Solórzano, G., Lei, Q., Kim, D., & Bayliss, D. A. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-19-07491.2001 · Cited by 573
Self-citation
Metadata
- Authors
- Rekling, J. C., Funk, G. D., Bayliss, D. A., Dong, X.-W., & Feldman, J. L.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2000-01-04
- Volume
- 80
- Issue
- 2
- Pages
- 767-852
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2110655603
- Cited by
- 607
- References
- 24
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- green
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