 |
Previous Article | Next Article 
The Journal of Neuroscience, November 1, 1998, 18(21):9055-9068
Anesthetics Eliminate Somatosensory-Evoked Discharges of Neurons
in the Somatotopically Organized Sensorimotor Striatum of the Rat
Mark O.
West
Department of Psychology, Rutgers University, New Brunswick,
New Jersey 08903
The somatotopic organization of the lateral striatum has been
demonstrated by anatomical studies of corticostriatal projections from
somatosensory and motor cortices and by single-cell recordings in awake
animals. The functional organization in the rat, characterized thus far
in the freely moving rat preparation, could be mapped more precisely if
a stereotaxic, and possibly an anesthetized, preparation could be used.
Because striatal discharges evoked by innocuous somatosensory
stimulation are used in mapping, this study tested whether such
discharges can be observed during anesthesia, encouraged by
responsiveness during anesthesia in somatosensory cortical layers
projecting to the striatum. Electrode tracks through lateral striatum
of anesthetized rats (pentobarbital or ketamine) revealed spontaneously
discharging neurons but no discharges evoked by somatosensory
examination (passive manipulation and cutaneous stimulation of
14 body parts). Similar tracks in chronically implanted rats
showed evoked firing at numerous sites during wakefulness but not
during anesthesia (pentobarbital or urethane). Comparisons of the
activity of individual neurons between wakefulness and anesthesia
showed that pentobarbital, ketamine, chloral hydrate, urethane, or
metofane eliminated evoked firing and suppressed spontaneous firing.
Recovery time was greater for neural than for behavioral measures.
Thus, mapping as proposed is ruled out, and more importantly, the data
show that somatotopically organized lateral striatal neurons stop
discharging in response to natural stimulation during anesthesia.
Available data indicate they do not reach threshold in response to
depolarizations produced by glutamatergic corticostriatal synaptic
transmission projected from the somatosensory cortex. These data and
demonstrations of anesthetic-induced imbalances in most striatal
neurotransmitters emphasize that many results regarding striatal
physiology and pharmacology during anesthesia cannot be extrapolated to
behavioral conditions, thus indicating the need for more empirical
testing in conscious animals.
Key words:
striatum; putamen; somatosensory; anesthesia; neurons; corticostriatal; neurophysiology
Copyright © 1998 Society for Neuroscience 0270-6474/98/18219055-14$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
C. Tang, T. Mittler, D. C. Duke, Y. Zhu, A. P. Pawlak, and M. O. West
Dose- and Rate-Dependent Effects of Cocaine on Striatal Firing Related to Licking
J. Pharmacol. Exp. Ther.,
February 1, 2008;
324(2):
701 - 713.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Bengtsson and H. Jorntell
Ketamine and Xylazine Depress Sensory-Evoked Parallel Fiber and Climbing Fiber Responses
J Neurophysiol,
September 1, 2007;
98(3):
1697 - 1705.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Drouin, M. Page, and B. Waterhouse
Methylphenidate Enhances Noradrenergic Transmission and Suppresses Mid- and Long-Latency Sensory Responses in the Primary Somatosensory Cortex of Awake Rats
J Neurophysiol,
August 1, 2006;
96(2):
622 - 632.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Iwa, M. Matsushima, Y. Nakade, T. N. Pappas, M. Fujimiya, and T. Takahashi
Electroacupuncture at ST-36 accelerates colonic motility and transit in freely moving conscious rats
Am J Physiol Gastrointest Liver Physiol,
February 1, 2006;
290(2):
G285 - G292.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. F. Cheer, M. L. A. V. Heien, P. A. Garris, R. M. Carelli, and R. M. Wightman
Simultaneous dopamine and single-unit recordings reveal accumbens GABAergic responses: Implications for intracranial self-stimulation
PNAS,
December 27, 2005;
102(52):
19150 - 19155.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Sharott, P. J Magill, J. P. Bolam, and P. Brown
Directional analysis of coherent oscillatory field potentials in the cerebral cortex and basal ganglia of the rat
J. Physiol.,
February 1, 2005;
562(3):
951 - 963.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Bouairi, R. Neff, C. Evans, A. Gold, M. C. Andresen, and D. Mendelowitz
Respiratory sinus arrhythmia in freely moving and anesthetized rats
J Appl Physiol,
October 1, 2004;
97(4):
1431 - 1436.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. Hayashi
Exercise pressor reflex in decerebrate and anesthetized rats
Am J Physiol Heart Circ Physiol,
June 1, 2003;
284(6):
H2026 - H2033.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Pain, L. Besret, F. Vaufrey, M.-C. Gregoire, L. Pinot, P. Gervais, L. Ploux, G. Bloch, R. Mastrippolito, P. Laniece, et al.
In vivo quantification of localized neuronal activation and inhibition in the rat brain using a dedicated high temporal-resolution beta +-sensitive microprobe
PNAS,
August 6, 2002;
99(16):
10807 - 10812.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Vahle-Hinz and O. Detsch
What can in vivo electrophysiology in animal models tell us about mechanisms of anaesthesia?
Br. J. Anaesth.,
July 1, 2002;
89(1):
123 - 142.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Nakao, J. Gotoh, T.-Y. Kuang, D. M. Cohen, K. D. Pettigrew, and L. Sokoloff
Cerebral Blood Flow Responses to Somatosensory Stimulation Are Unaffected by Scopolamine in Unanesthetized Rat
J. Pharmacol. Exp. Ther.,
August 1, 1999;
290(2):
929 - 934.
[Abstract]
[Full Text]
|
 |
|
|