The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Cable properties of cat spinal motoneurones measured by combining voltage clamp, current clamp and intracellular staining.
Open accessAbstract
1. Spinal alpha‐motoneurones were injected with horseradish peroxidase after measuring their voltage response to a brief current pulse and their current response to a small voltage step. 2. The morphology of each motoneurone was reconstructed from serial sections. The diameters and lengths of dendritic segments were used to build a compartmental model of each neurone's electrotonic structure. The specific resistivity of the membrane (Rm) was assumed to be constant throughout the dendrites, but it was lowered for the somatic membrane by the introduction of a somatic shunt resistance. 3. The specific resistances of the somatic and dendritic membrane were adjusted in the compartmental model until the responses of the model to the same current and voltage steps as those used in the experiment gave the best fits to the recorded transients. Satisfactory fits were obtained for six out of seven motoneurones. Dendritic Rm varied from 7 to 35 k omega cm2 and somatic Rm varied from 100 to 420 omega cm2. The dendritic Rm was 100‐300 times the somatic Rm for different neurones. 4. The calculated dendritic Rm was used to determine the geometric profile of the equivalent dendritic cable. This was found to be an approximately uniform cylinder for about 0.5 lambda and thereafter to taper rapidly to a final termination at 2‐3 lambda from the soma. 5. The results indicate that motoneurone dendrites are more electrically compact than was hitherto believed. The different Rm values for somatic and dendritic membrane, and the tapering of the dendritic cable, means that the cable model developed by Rall (1959, 1964) must be revised to take account of these spatial and electrical non‐uniformities.
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Citations
Cites
Branching dendritic trees and motoneuron membrane resistivity
Rall, W. (1959) · Experimental Neurology · doi:10.1016/0014-4886(59)90046-9 · Cited by 1,009
Rall, W. (1967) · Journal of Neurophysiology · doi:10.1152/jn.1967.30.5.1138 · Cited by 992
Technical considerations on the use of horseradish peroxidase as a neuronal marker
Adams, J. C. (1977) · Neuroscience · doi:10.1016/0306-4522(77)90074-4 · Cited by 914
Theory of Physiological Properties of Dendrites
Rall, W. (1962) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1962.tb54120.x · Cited by 594
Retinal ganglion cells: a functional interpretation of dendritic morphology
Koch, C., Poggio, T., & Torre, V. (1982) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1982.0084 · Cited by 420
Membrane potential transients and membrane time constant of motoneurons
Rall, W. (1960) · Experimental Neurology · doi:10.1016/0014-4886(60)90029-7 · Cited by 295
Specific membrane properties of cat motoneurones
Barrett, J. N., & Crill, W. E. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010570 · Cited by 281
Interpretation of voltage-clamp measurements in hippocampal neurons
Johnston, D., & Brown, T. H. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.50.2.464 · Cited by 254
Electrotonic architecture of type-identified alpha-motoneurons in the cat spinal cord
Fleshman, J. W., Segev, I., & Burke, R. B. (1988) · Journal of Neurophysiology · doi:10.1152/jn.1988.60.1.60 · Cited by 229
Glutamate‐induced increase in intracellular Ca2+ concentration in isolated hippocampal neurones
Kudo, Y., & Ogura, A. (1986) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1986.tb11135.x · Cited by 216
Cited by
Jonas, P., Major, G., & Sakmann, B. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019965 · Cited by 720
Propagation of action potentials in dendrites depends on dendritic morphology
Vetter, P., Roth, A., & Häusser, M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.926 · Cited by 598
Changes in the structural complexity of the aged brain
Dickstein, D. L., Kabaso, D., Rocher, A. B., Luebke, J. I., Wearne, S. L., & Hof, P. R. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00289.x · Cited by 460
Roth, A., & Häusser, M. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00445.x · Cited by 278
A large pool of releasable vesicles in a cortical glutamatergic synapse
Hallermann, S., Pawlu, C., Jonas, P., & Heckmann, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1432836100 · Cited by 181
Metadata
- Authors
- Clements, J. D., & Redman, S. J.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 1989-02
- Volume
- 409
- Issue
- 1
- Pages
- 63-87
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- OpenAlex
- W2094169507
- Cited by
- 301
- References
- 28
- FWCI
- 19.39
- Type
- journal article
- Language
- en
- Open access
- green
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- Clements, J. D., & Redman, S. J. (1989). Cable properties of cat spinal motoneurones measured by combining voltage clamp, current clamp and intracellular staining. The Journal of Physiology. https://doi.org/10.1113/jphysiol.1989.sp017485
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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