Homosynaptic depression and transmitter turnover in spinal monosynaptic pathway
- PMID: 13160
- DOI: 10.1152/jn.1977.40.1.95
Homosynaptic depression and transmitter turnover in spinal monosynaptic pathway
Abstract
1. The transmission in the spinal monosynaptic pathway was studied during repetitive stimulation of a motor nerve by 10 stimuli at 2, 5, or 10 Hz in spinal cats. Initially, the amplitudes of the monosynaptic responses rapidly declined, reaching a plateau after a few stimuli. The level of the plateau was inversely related to the frequency of stimulation. 2. This depression of monosynaptic response was seen only when the same pathway was stimulated; the response elicited from the lateral gastrocnemius was not depressed when preceded by stimulation of the medial gastrocnemius nerve and vice versa. Pretreatment with semicarbazide left the homosynaptic depression unchanged while suppressing the dorsal root reflex. The participation of a depolarization of primary afferents in the described depression is, therefore, unlikely. 3. The decrease of transmitter release by successive volleys, which is the cause of the observed depression, could conceivably be related to the depletion of transmitter stores. 4. A procedure is described, based on this assumption, which allows the calculation of transmitter turnover. The input-output relation in the spinal monosynaptic pathway is used to convert the amplitudes of monosynaptic responses to the amounts of transmitter, both relative to the maximum response. The changes of transmitter release are analyzed under the assumption that each volley releases instantaneously a constant fraction of the transmitter store available for release and that this store is replenished at a constant fraction of the depleted part per second. 5. The values of fractional release per volley were about 0.4, irrespective of frequency of stimulation. 6. The values of fractional replenishment per second ranged from about 1 to 5 on the average, depending directly on the frequency of stimulation. 7. It is suggested that the described procedure might be useful in analyzing drug effects on synaptic transmission.
Similar articles
-
Effects of ethosuximide on transmission of repetitive impulses and apparent rates of transmitter turnover in the spinal monosynaptic pathway.J Pharmacol Exp Ther. 1977 May;201(2):320-5. J Pharmacol Exp Ther. 1977. PMID: 16119
-
A GABAergic component in homosynaptic depression in the spinal monosynaptic pathway. A requirement for action of benzodiazepines.Neuropharmacology. 1985 Apr;24(4):309-16. doi: 10.1016/0028-3908(85)90136-4. Neuropharmacology. 1985. PMID: 2987725
-
Rates of transmitter turnover in spinal monosynaptic pathway investigated by electrophysiological techniques.J Neurophysiol. 1971 Sep;34(5):842-59. doi: 10.1152/jn.1971.34.5.842. J Neurophysiol. 1971. PMID: 4398563 No abstract available.
-
Baclofen-induced decrease of excitability of primary afferents and depression of monosynaptic transmission in cat spinal cord.Can J Physiol Pharmacol. 1982 Feb;60(2):160-6. doi: 10.1139/y82-026. Can J Physiol Pharmacol. 1982. PMID: 6282427
-
Developmental changes in short-term synaptic depression in the neonatal mouse spinal cord.J Neurophysiol. 2002 Dec;88(6):3218-31. doi: 10.1152/jn.00406.2002. J Neurophysiol. 2002. PMID: 12466442
Cited by
-
A comparative study of methods for estimation of presynaptic inhibition.J Neurol. 1992 May;239(5):287-92. doi: 10.1007/BF00810355. J Neurol. 1992. PMID: 1607893
-
Transient analysis of a chemical synaptic transmission.Biol Cybern. 1993;68(4):341-50. doi: 10.1007/BF00201859. Biol Cybern. 1993. PMID: 8097407
-
Sensitization and habituation of dorsal horn cells in cats.J Physiol. 1978 Jun;279:153-66. doi: 10.1113/jphysiol.1978.sp012337. J Physiol. 1978. PMID: 671348 Free PMC article.
-
The effect of age on post-activation depression of the upper limb H-reflex.Eur J Appl Physiol. 2014 Feb;114(2):359-64. doi: 10.1007/s00421-013-2778-5. Epub 2013 Dec 1. Eur J Appl Physiol. 2014. PMID: 24292018
-
Recovery of stretch reflex responses following mechanical stimulation.Eur J Appl Physiol Occup Physiol. 1993;66(5):415-20. doi: 10.1007/BF00599614. Eur J Appl Physiol Occup Physiol. 1993. PMID: 8330609
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous