» Articles » PMID: 3384047

Sustained Excitatory Synaptic Input to Motor Cortex Neurons in Awake Animals Revealed by Intracellular Recording of Membrane Potentials

Overview
Journal Exp Brain Res
Specialty Neurology
Date 1988 Jan 1
PMID 3384047
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

1. Most of the intracellular electrophysiological data on cortical neurons has been obtained in anesthetized or reduced preparations, and differs from observations in awake, intact animals. To determine whether these differences are due to experimental techniques or physiological factors, we recorded membrane potentials intracellularly from motor cortex neurons in chronically prepared cats and monkeys under Nembutal-anesthetized, Halothane-anesthetized, and unanesthetized conditions, or during transitions between anesthetized and awake conditions. 2. Resting membrane potentials were found to depend on the anesthetic state of the animal. Membrane potentials of neurons recorded in awake animals were more depolarized than those recorded in the anesthetized state. In the awake state membrane potentials were all less than -65 mV. 3. The input resistance of neurons recorded in awake animals were significantly smaller than those measured in the anesthetized state. Action potentials recorded in awake animals typically showed an undershoot (i.e. negative values at peak), implying that voltage-dependent conductances may be altered. Undershoot of the action potential was more prominent in pyramidal tract neurons (PTNs) than non-PTNs. 4. These data suggested that in awake animals motor cortex neurons, especially PTNs, receive sustained excitatory synaptic input or neuro-modulatory activities.

Citing Articles

Noise Enhancement of Neural Information Processing.

Destexhe A Entropy (Basel). 2022; 24(12).

PMID: 36554242 PMC: 9778153. DOI: 10.3390/e24121837.


Subthreshold Activity Underlying the Diversity and Selectivity of the Primary Auditory Cortex Studied by Intracellular Recordings in Awake Marmosets.

Gao L, Wang X Cereb Cortex. 2018; 29(3):994-1005.

PMID: 29377991 PMC: 6373684. DOI: 10.1093/cercor/bhy006.


A Statistical Model for In Vivo Neuronal Dynamics.

Surace S, Pfister J PLoS One. 2015; 10(11):e0142435.

PMID: 26571371 PMC: 4646699. DOI: 10.1371/journal.pone.0142435.


What is all the noise about in interval timing?.

Oprisan S, Buhusi C Philos Trans R Soc Lond B Biol Sci. 2014; 369(1637):20120459.

PMID: 24446493 PMC: 3895984. DOI: 10.1098/rstb.2012.0459.


Why noise is useful in functional and neural mechanisms of interval timing?.

Oprisan S, Buhusi C BMC Neurosci. 2013; 14:84.

PMID: 23924391 PMC: 3751097. DOI: 10.1186/1471-2202-14-84.


References
1.
Woody C . Differences in excitability of cortical neurons as a function of motor projection in conditioned cats. J Neurophysiol. 1973; 36(6):1104-16. DOI: 10.1152/jn.1973.36.6.1104. View

2.
Morales F, Chase M . Intracellular recording of lumbar motoneuron membrane potential during sleep and wakefulness. Exp Neurol. 1978; 62(3):821-7. DOI: 10.1016/0014-4886(78)90289-3. View

3.
Li C . Cortical intracellular potentials and their responses to strychnine. J Neurophysiol. 1959; 22(4):436-50. DOI: 10.1152/jn.1959.22.4.436. View

4.
Nicoll R, Madison D . General anesthetics hyperpolarize neurons in the vertebrate central nervous system. Science. 1982; 217(4564):1055-7. DOI: 10.1126/science.7112112. View

5.
Evarts E . TEMPORAL PATTERNS OF DISCHARGE OF PYRAMIDAL TRACT NEURONS DURING SLEEP AND WAKING IN THE MONKEY. J Neurophysiol. 1964; 27:152-71. DOI: 10.1152/jn.1964.27.2.152. View