JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 76: 1101-1111, 1996;
0022-3077/96 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sanchez, R.
Right arrow Articles by Leonard, C. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sanchez, R.
Right arrow Articles by Leonard, C. S.

Journal of Neurophysiology, Vol 76, Issue 2 1101-1111, Copyright © 1996 by APS


ARTICLES

NMDA-receptor-mediated synaptic currents in guinea pig laterodorsal tegmental neurons in vitro

R. Sanchez and C. S. Leonard
Center for Neural Science, New York University, New York 10003, USA.

1. Whole cell voltage-clamp techniques were used to record glutamate-receptor-mediated synaptic currents from neurons of the laterodorsal tegmental nucleus (LDT). The principal cells of the LDT contain acetylcholine and nitric oxide synthase, and are believed to be involved in the control of sleep-waking behavior via widespread projections to the thalamus and brain stem. LDT cells were recorded from slices of mature guinea pig brain stem with patch pipette solutions containing cesium as the primary cation. 2. Application of N-methyl-D-aspartate (NMDA) elicited currents that were strongly voltage dependent with a mean reversal potential of +16.3 mV. Peak currents occurred near -15 mV, and a region of negative slope conductance was seen at more negative potentials. Application of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid evoked currents that exhibited a nearly linear current-voltage relation with a mean reversal potential of -3.4 mV. 3. Electrical stimulation of local afferents elicited dual-component excitatory postsynaptic currents (EPSCs) with decays that were well fitted by the sum of two exponentials. Mean decay time constants at -60 mV were 8.77 ms for the faster component and 129.4 ms for the slower component. The faster component displayed a linear current-voltage relation and was blocked by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) or 6,7-dinitroquinoxaline-2,3-dione, indicating that it was mediated by non-NMDA receptors, whereas the slower component displayed a voltage dependence similar to that for NMDA-evoked currents and was blocked by 2-amino-5-phosphonopentanoic acid (AP-5), indicating its mediation by NMDA receptors. 4. The fractional contribution of NMDA receptors to the EPSC was estimated from double-exponential curve fits to the decay phases. With this method, NMDA receptors were estimated on average to carry 10.1% of the total peak EPSC at -60 mV. Blockade of the non-NMDA-receptor-mediated component with CNQX revealed a residual EPSC whose amplitude was 14.4% of the control value, whereas AP-5 alone reduced the control EPSC peak by 16.1%, both values were comparable with those obtained from curve fit estimates. 5. Previous work has shown that the presence of 4-aminopyridine-sensitive, A-like transient current in LDT cells is correlated with the cholinergic phenotype. The majority of cells in this study exhibited A-like transient currents that were blocked by 4-amino-pyridine, suggesting that the majority of the data were obtained from the cholinergic and NOS-containing neurons of the LDT nucleus. 6. These experiments demonstrate the synaptic activation of functional NMDA and non-NMDA receptors in LDT neurons, and indicate that NMDA receptors contribute to fast excitatory transmission in these cells. The results suggest that afferents releasing excitatory amino acids may play an important role in controlling the state-dependent activity of LDT neurons.


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
K. A. Kohlmeier, T. Inoue, and C. S. Leonard
Hypocretin/Orexin Peptide Signaling in the Ascending Arousal System: Elevation of Intracellular Calcium in the Mouse Dorsal Raphe and Laterodorsal Tegmentum
J Neurophysiol, July 1, 2004; 92(1): 221 - 235.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
T. Kobayashi, C. Good, K. Mamiya, R. D. Skinner, and E. Garcia-Rill
Development of REM sleep drive and clinical implications
J Appl Physiol, February 1, 2004; 96(2): 735 - 746.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. S. Leonard, E. K. Michaelis, and K. M. Mitchell
Activity-Dependent Nitric Oxide Concentration Dynamics in the Laterodorsal Tegmental Nucleus In Vitro
J Neurophysiol, November 1, 2001; 86(5): 2159 - 2172.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
E. Arrigoni, D. G. Rainnie, R. W. McCarley, and R. W. Greene
Adenosine-Mediated Presynaptic Modulation of Glutamatergic Transmission in the Laterodorsal Tegmentum
J. Neurosci., February 1, 2001; 21(3): 1076 - 1085.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. S. Leonard, S. R. Rao, and T. Inoue
Serotonergic Inhibition of Action Potential Evoked Calcium Transients in NOS-Containing Mesopontine Cholinergic Neurons
J Neurophysiol, September 1, 2000; 84(3): 1558 - 1572.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. M. Sanchez, A. Surkis, and C. S. Leonard
Voltage-Clamp Analysis and Computer Simulation of a Novel Cesium-Resistant A-Current in Guinea Pig Laterodorsal Tegmental Neurons
J Neurophysiol, June 1, 1998; 79(6): 3111 - 3126.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online