PROPERTIES OF THE HYPERPOLARIZATION-ACTIVATED CURRENT IN RAT HIPPOCAMPAL CA1 PYRAMIDAL CELLS

被引:220
作者
MACCAFERRI, G [1 ]
MANGONI, M [1 ]
LAZZARI, A [1 ]
DIFRANCESCO, D [1 ]
机构
[1] UNIV MILAN,DIPARTIMENTO FIS & BIOCHIM GEN,I-20133 MILAN,ITALY
关键词
D O I
10.1152/jn.1993.69.6.2129
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Voltage and current clamp recordings were performed on CA 1 rat hippocampal pyramidal cells using the patch clamp technique on ''in vitro'' slice preparations. 2. Hyperpolarizations from a holding potential of -35 mV elicited activation of the hyperpolarization-activated current (I(h)) starting at voltages near -50 mV. 3. 1, recorded in voltage clamp conditions was blocked by external caesium (5 mM). 4. Raising the external K concentration from 4.35 to 24.35 mM sensibly increased the slope of the current-voltage (I/V) curve. Decreasing the external Na concentration from 133.5 to 33.5 mM depressed I(h) without grossly altering the I/V slope. 5. The I(h) fully activated I/V relation measured in the range -140 to -45 mV was linear with an extrapolated reversal at -17.0 +/- -1.6 (SE) mV. The current activation curve comprised the range between about -50 and -140 mV with a half-maximal activation at about -98 mV. 6. Perfusion of unclamped neurons with Cs (2 mM) hyperpolarized their resting potential by 3.8 +/- 0.2 mV and decreased the membrane conductance, as expected if 1, were activated at rest. Firing caused by depolarizing current steps was prevented by Cs-induced hyperpolarization, and could be restored by returning the membrane voltage to resting level by constant current injection. 7. The Cd-insensitive (medium-duration) afterhyperpolarization (AHP) elicited by a train of action potentials at -60 mV had an amplitude of 3.9 +/- 0.3 mV and was nearly fully abolished by 2 mM Cs (82.7 +/- 7.4%). Cs removed the depolarizing part of the afterhyperpolarization as expected if I(h) activation was responsable for this phase. 8. These results indicate that in CA1 hippocampal pyramidal neurons, the current Ih is tonically active at resting potentials and contributes to controlling afterhyperpolarizations and cell excitability.
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页码:2129 / 2136
页数:8
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