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多种离子机制介导吸入麻醉剂对大鼠运动神经元的抑制作用。

Multiple ionic mechanisms mediate inhibition of rat motoneurones by inhalation anaesthetics.

作者信息

Sirois J E, Pancrazio J J, Lynch C, Bayliss D A

机构信息

Department of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.

出版信息

J Physiol. 1998 Nov 1;512 ( Pt 3)(Pt 3):851-62. doi: 10.1111/j.1469-7793.1998.851bd.x.

Abstract
  1. We studied the effects of inhalation anaesthetics on the membrane properties of hypoglossal motoneurones in a neonatal rat brainstem slice preparation. 2. In current clamp, halothane caused a membrane hyperpolarization that was invariably associated with decreased input resistance; in voltage clamp, halothane induced an outward current and increased input conductance. Qualitatively similar results were obtained with isoflurane and sevoflurane. 3. The halothane current reversed near the predicted K+ equilibrium potential (EK) and was reduced in elevated extracellular K+ and in the presence of Ba2+ (2 mM). Moreover, the Ba2+-sensitive component of halothane current was linear and reversed near EK. The halothane current was not sensitive to glibenclamide or thyrotropin-releasing hormone (TRH). Therefore, the halothane current was mediated, in part, by activation of a Ba2+-sensitive K+ current distinct from the ATP- and neurotransmitter-sensitive K+ currents in hypoglossal motoneurones. 4. Halothane also inhibited Ih, a hyperpolarization-activated cationic current; this was primarily due to a decrease in the absolute amount of current, although halothane also caused a small, but statistically significant, shift in the voltage dependence of Ih activation. Extracellular Cs+ (3 mM) blocked Ih and a component of halothane-sensitive current with properties reminiscent of Ih. 5. A small component of halothane current, resistant to Ba2+ and Cs+, was observed in TTX-containing solutions at potentials depolarized to approximately -70 mV. Partial Na+ substitution by N-methyl-D-glucamine completely abolished this residual current, indicating that halothane also inhibited a TTX-resistant Na+ current active near rest potentials. 6. Thus, halothane activates a Ba2+-sensitive, relatively voltage-independent K+ current and inhibits both Ih and a TTX-insensitive persistent Na+ current in hypoglossal motoneurones. These effects of halothane decrease motoneuronal excitability and may contribute to the immobilization that accompanies inhalation anaesthesia.
摘要
  1. 我们在新生大鼠脑干切片标本中研究了吸入麻醉药对舌下运动神经元膜特性的影响。2. 在电流钳模式下,氟烷引起膜超极化,这总是与输入电阻降低相关;在电压钳模式下,氟烷诱导外向电流并增加输入电导。异氟烷和七氟烷也得到了定性相似的结果。3. 氟烷电流在接近预测的钾离子平衡电位(EK)处反转,并且在细胞外钾离子浓度升高和存在钡离子(2 mM)时减小。此外,氟烷电流的钡离子敏感成分呈线性且在EK附近反转。氟烷电流对格列本脲或促甲状腺激素释放激素(TRH)不敏感。因此,氟烷电流部分是由激活一种与舌下运动神经元中ATP敏感和神经递质敏感钾电流不同的钡离子敏感钾电流介导的。4. 氟烷还抑制Ih,一种超极化激活的阳离子电流;这主要是由于电流绝对值的降低,尽管氟烷也导致Ih激活的电压依赖性有一个小的但具有统计学意义的偏移。细胞外铯离子(3 mM)阻断Ih和一种具有Ih特性的氟烷敏感电流成分。5. 在含有河豚毒素(TTX)的溶液中,当电位去极化到约-70 mV时,观察到一小部分对钡离子和铯离子有抗性的氟烷电流。用N-甲基-D-葡萄糖胺部分替代钠离子完全消除了这种残余电流,表明氟烷也抑制了静息电位附近活跃的一种对TTX有抗性的钠离子电流。6. 因此,氟烷激活一种钡离子敏感、相对电压不依赖的钾电流,并抑制舌下运动神经元中的Ih和一种对TTX不敏感的持续性钠离子电流。氟烷的这些作用降低了运动神经元的兴奋性,并可能导致吸入麻醉时的肌肉松弛。

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