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大鼠海马CA1锥体神经元超极化激活电流的特性

Properties of the hyperpolarization-activated current in rat hippocampal CA1 pyramidal cells.

作者信息

Maccaferri G, Mangoni M, Lazzari A, DiFrancesco D

机构信息

Dipartimento di Fisiologia e Biochimica Generali, Università di Milano, Italy.

出版信息

J Neurophysiol. 1993 Jun;69(6):2129-36. doi: 10.1152/jn.1993.69.6.2129.

Abstract
  1. Voltage and current clamp recordings were performed on CA1 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 (Ih) starting at voltages near -50 mV. 3. Ih 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 Ih without grossly altering the I/V slope. 5. The Ih 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 Ih 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 Ih activation was responsible for this phase.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 使用膜片钳技术,在“体外”脑片标本上对大鼠CA1海马锥体神经元进行电压钳和电流钳记录。2. 从 -35 mV的钳制电位开始超极化,在接近 -50 mV的电压时可引发超极化激活电流(Ih)的激活。3. 在电压钳条件下记录的Ih可被细胞外铯(5 mM)阻断。4. 将细胞外钾浓度从4.35 mM提高到24.35 mM可显著增加电流 - 电压(I/V)曲线的斜率。将细胞外钠浓度从133.5 mM降低到33.5 mM可抑制Ih,但对I/V斜率无明显改变。5. 在 -140至 -45 mV范围内测量的Ih完全激活时的I/V关系呈线性,外推反转电位为 -17.0± -1.6(SE)mV。电流激活曲线范围约为 -50至 -140 mV,半最大激活电位约为 -98 mV。6. 用铯(2 mM)灌流未钳制的神经元,其静息电位超极化3.8±0.2 mV,并降低膜电导,这与Ih在静息时被激活的预期相符。铯诱导的超极化可防止去极化电流脉冲引发的放电,通过恒流注入将膜电压恢复到静息水平可恢复放电。7. 在 -60 mV时,一串动作电位引发的对镉不敏感(中等时程)的后超极化(AHP)幅度为3.9±0.3 mV,2 mM铯可使其几乎完全消除(82.7±7.4%)。如果Ih激活是该阶段的原因,铯可如预期那样消除后超极化的去极化部分。(摘要截断于250字)

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