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The Journal of Neurophysiology Vol. 85 No. 5 May 2001, pp. 2063-2069
Copyright ©2001 by the American Physiological Society
1Johannes-Müller-Institut für Physiologie, Humboldt Universität Berlin, 10117 Berlin, Germany; and 2Department of Biosciences, Division of Animal Physiology, University of Helsinki, Fin-00014 Helsinki, Finland
Stenkamp, Kerstin,
J. Matias Palva,
Marylka Uusisaari,
Sebastian Schuchmann,
Dietmar Schmitz,
Uwe Heinemann, and
Kai Kaila.
Enhanced Temporal Stability of Cholinergic Hippocampal Gamma
Oscillations Following Respiratory Alkalosis In Vitro. J. Neurophysiol. 85: 2063-2069, 2001. The
decrease in brain CO2 partial pressure (pCO2)
that takes place both during voluntary and during pathological
hyperventilation is known to induce gross alterations in cortical
functions that lead to subjective sensations and altered states of
consciousness. The mechanisms that mediate the effects of the decrease
in pCO2 at the neuronal network level are largely
unexplored. In the present work, the modulation of gamma oscillations
by hypocapnia was studied in rat hippocampal slices. Field potential
oscillations were induced by the cholinergic agonist carbachol under an
N-methyl-D-aspartate (NMDA)-receptor
blockade and were recorded in the dendritic layer of the CA3 region
with parallel measurements of changes in interstitial and intraneuronal
pH (pHo and pHi, respectively). Hypocapnia from 5 to 1% CO2 led to a stable monophasic increase of 0.5 and
0.2 units in pHo and pHi, respectively. The
mean oscillation frequency increased slightly but significantly from 32 to 34 Hz and the mean gamma-band amplitude (20 to 80 Hz) decreased by
20%. Hypocapnia induced a dramatic enhancement of the temporal
stability of the oscillations, as was indicated by a two-fold increase
in the exponential decay time constant fitted to the autocorrelogram. A
rise in pHi evoked by the weak base trimethylamine (TriMA)
was associated with a slight increase in oscillation frequency (37 to
39 Hz) and a decrease in amplitude (30%). Temporal stability, on the other hand, was decreased by TriMA, which suggests that its enhancement in 1% CO2 was related to the rise in pHo. In
1% CO2, the decay-time constant of the evoked monosynaptic
pyramidal inhibitory postsynaptic current (IPSC) was unaltered but its
amplitude was enhanced. This increase in IPSC amplitude seems to
significantly contribute to the enhancement of temporal stability
because the enhancement was almost fully reversed by a low
concentration of bicuculline. These results suggest that changes in
brain pCO2 can have a strong influence on the temporal
modulation of gamma rhythms.
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