Whole-Body Rotations Enhance Hippocampal Theta Rhythmic Slow Activity in Awake Rats Passively Transported on a Mobile Robot

1996 ◽  
Vol 781 (1 Lipids and Sy) ◽  
pp. 385-398 ◽  
Author(s):  
VLADIMIR V. GAVRILOV ◽  
SIDNEY I. WIENER ◽  
ALAIN BERTHOZ
2003 ◽  
Vol 89 (2) ◽  
pp. 1057-1066 ◽  
Author(s):  
Ian D. Manns ◽  
Angel Alonso ◽  
Barbara E. Jones

The basal forebrain plays important roles in arousal, learning, and memory by stimulating cortical activation characterized by rhythmic slow theta and high-frequency beta-gamma activities. Although cholinergic neurons play a significant part in these roles, other, including GABAergic, neurons appear to contribute. Using juxtacellular labeling with neurobiotin of neurons recorded within the magnocellular preoptic-substantia innominata area in urethan-anesthetized rats, we show that in addition to cells that are cholinergic or GABAergic, other cells that are neither fire rhythmically in correlation with stimulation-induced rhythmic slow activity on the cortex. Neurons with the characteristics of the noncholinergic/nonGABAergic cells contain phosphate-activated glutaminase (PAG), the synthetic enzyme for transmitter glutamate and may thus be glutamatergic. Within their oscillatory spike trains, putative glutamatergic neurons fire at a lower frequency (∼20 Hz) than the GABAergic neurons (∼40 Hz) and the cholinergic neurons (average: 75 Hz), whose spike trains include high-frequency bursts. The three groups all discharge rhythmically at a slow frequency in correlation with rhythmic slow activity recorded on the prefrontal, entorhinal, piriform and olfactory bulb cortices. The predominant slow frequency corresponds to the respiratory-olfactory rhythm, which is commonly slower than, yet can be as fast as, the hippocampal theta rhythm during certain coordinated behaviors, such as sniffing-whisking. While stimulating higher frequency beta-gamma activities, putative glutamatergic together with GABAergic and cholinergic cells may thus collectively modulate rhythmic slow activity and thereby promote coherent processing and plasticity across distributed cortical networks during coordinated behaviors and states.


1997 ◽  
Vol 82 (2) ◽  
pp. 469-479 ◽  
Author(s):  
Manjapra R. Akilesh ◽  
Matthew Kamper ◽  
Aihua Li ◽  
Eugene E. Nattie

Akilesh, Manjapra R., Matthew Kamper, Aihua Li, and Eugene E. Nattie. Effects of unilateral lesions of retrotrapezoid nucleus on breathing in awake rats. J. Appl. Physiol. 82(2): 469–479, 1997.—In anesthetized rats, unilateral retrotrapezoid nucleus (RTN) lesions markedly decreased baseline phrenic activity and the response to CO2 (E. E. Nattie and A. Li. Respir. Physiol. 97: 63–77, 1994). Here we evaluate the effects of such lesions on resting breathing and on the response to hypercapnia and hypoxia in unanesthetized awake rats. We made unilateral injections [24 ± 7 (SE) nl] of ibotenic acid (IA; 50 mM), an excitatory amino acid neurotoxin, in the RTN region ( n = 7) located by stereotaxic coordinates and by field potentials induced by facial nerve stimulation. Controls ( n = 6) received RTN injections (80 ± 30 nl) of mock cerebrospinal fluid. A second control consisted of four animals with IA injections (24 ± 12 nl) outside the RTN region. Injected fluorescent beads allowed anatomic identification of lesion location. Using whole body plethysmography, we measured ventilation in the awake state during room air, 7% CO2 in air, and 10% O2 breathing before and for 3 wk after the RTN injections. There was no statistically significant effect of the IA injections on resting room air breathing in the lesion group compared with the control groups. We observed no apnea. The response to 7% CO2 in the lesion group compared with the control groups was significantly decreased, by 39% on average, for the final portion of the 3-wk study period. There was no lesion effect on the ventilatory response to 10% O2. In this unanesthetized model, other areas suppressed by anesthesia, e.g., the reticular activating system, hypothalamus, and perhaps the contralateral RTN, may provide tonic input to the respiratory centers that counters the loss of RTN activity.


1995 ◽  
Vol 197 (3) ◽  
pp. 239-241 ◽  
Author(s):  
Vladimir V. Gavrilov ◽  
Sidney I. Wiener ◽  
Alain Berthoz
Keyword(s):  

1992 ◽  
Vol 578 (1-2) ◽  
pp. 13-16 ◽  
Author(s):  
Jan Konopacki ◽  
Henryk Gołebiewski ◽  
Barbara Eckersdorf

2001 ◽  
Vol 90 (5) ◽  
pp. 1729-1735 ◽  
Author(s):  
Richard Kinkead ◽  
Lydie Dupenloup ◽  
Nadine Valois ◽  
Roumiana Gulemetova

To test the hypothesis that stress alters the performance of the respiratory control system, we compared the acute (20 min) responses to moderate hypoxia and hypercapnia of rats previously subjected to immobilization stress (90 min/day) with responses of control animals. Ventilatory measurements were performed on awake rats using whole body plethysmography. Under baseline conditions, there were no differences in minute ventilation between stressed and unstressed groups. Rats previously exposed to immobilization stress had a 45% lower ventilatory response to hypercapnia (inspiratory CO2 fraction = 0.05) than controls. In contrast, stress exposure had no statistically significant effect on the ventilatory response to hypoxia (inspiratory O2 fraction = 0.12). Stress-induced attenuation of the hypercapnic response was associated with reduced tidal volume and inspiratory flow increases; the frequency and timing components of the response were not different between groups. We conclude that previous exposure to a stressful condition that does not constitute a direct challenge to respiratory homeostasis can elicit persistent (≥24 h) functional plasticity in the ventilatory control system.


1975 ◽  
pp. 101-128 ◽  
Author(s):  
C. H. Vanderwolf ◽  
R. Kramis ◽  
L. A. Gillespie ◽  
B. H. Bland

1987 ◽  
Vol 400 (2) ◽  
pp. 334-347 ◽  
Author(s):  
G. Buzsáki ◽  
F.H. Gage ◽  
J. Czopf ◽  
A. Björklund

1991 ◽  
Vol 44 (1) ◽  
pp. 35-41
Author(s):  
Takanori Suzuki ◽  
Yasufumi Nishimura ◽  
Teiichiro Tonoue

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