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异氟烷对丘脑皮质神经元作用的离子机制

Ionic mechanism of isoflurane's actions on thalamocortical neurons.

作者信息

Ries C R, Puil E

机构信息

Department of Anaesthesia, Faculty of Medicine, The University of British Columbia Vancouver, British Columbia V6T 1Z3 Canada.

出版信息

J Neurophysiol. 1999 Apr;81(4):1802-9. doi: 10.1152/jn.1999.81.4.1802.

Abstract

We studied the actions of isoflurane (IFL) applied in aqueous solutions on ventrobasal neurons from thalamic brain slices of juvenile rats. By using the whole cell, patch-clamp method with current- and voltage-clamp recording techniques, we found that IFL increased a noninactivating membrane conductance in a concentration-dependent reversible manner. In an eightfold concentration range that extended into equivalent in vivo lethal concentrations, IFL did not produce a maximal effect on the conductance; this is consistent with a nonreceptor-mediated mechanism of action. TTX eliminated action potential activity but did not alter IFL effects. The effects on the membrane potential and current induced by IFL were voltage independent but depended on the external [K+], reversing near the equilibrium potential for K+. External Ba2+ or internal Cs+ applications, which block K+ channels, suppressed the conductance increase caused by IFL. External applications of the Ca2+ channel blockers Co2+ or Cd2+ or internal application of the Ca2+ chelator 1,2-bis-(2-aminophenoxy)-ethane-N,N, N',N'-tetraacetic acid did not prevent the effects of IFL, implying little involvement of Ca2+-dependent K+ currents. A contribution of inwardly rectifying K+ channels to the increased steady-state conductance seemed unlikely because IFL decreased inward rectification. An involvement of ATP-mediated K+ channels also was unlikely because application of the ATP-mediated K+ channel blocker glibenclamide (1-80 microM) did not prevent IFL's actions. In contrast to spiking cells, IFL depolarized presumed glial cells, consistent with an efflux of K+ from thalamocortical neurons. The results imply that a leak K+ channel mediated the IFL-induced increase in postsynaptic membrane conductance in thalamic relay neurons. Thus a single nonreceptor-mediated mechanism of IFL action was responsible for the hyperpolarization and conductance shunt of voltage-dependent Na+ and Ca2+ spikes, as reported in the preceding paper. Although anesthetics influence various neurological systems, an enhanced K+ leak generalized in thalamocortical neurons alone could account for anesthesia in vivo.

摘要

我们研究了异氟烷(IFL)在水溶液中对幼年大鼠丘脑脑片腹侧基底神经元的作用。通过使用全细胞、膜片钳方法以及电流钳和电压钳记录技术,我们发现IFL以浓度依赖性可逆方式增加了一种非失活膜电导。在延伸至等效体内致死浓度的八倍浓度范围内,IFL对电导并未产生最大效应;这与非受体介导的作用机制一致。河豚毒素(TTX)消除了动作电位活动,但未改变IFL的作用。IFL对膜电位和电流的影响与电压无关,但取决于细胞外[K⁺],在K⁺平衡电位附近发生反转。应用阻断K⁺通道的细胞外Ba²⁺或细胞内Cs⁺可抑制IFL引起的电导增加。应用Ca²⁺通道阻滞剂Co²⁺或Cd²⁺或细胞内应用Ca²⁺螯合剂1,2 - 双 -(2 - 氨基苯氧基)乙烷 - N,N,N',N'-四乙酸并不能阻止IFL的作用,这表明Ca²⁺依赖性K⁺电流几乎没有参与其中。内向整流K⁺通道对稳态电导增加的贡献似乎不太可能,因为IFL降低了内向整流。ATP介导的K⁺通道参与其中的可能性也不大,因为应用ATP介导的K⁺通道阻滞剂格列本脲(1 - 80 μM)并不能阻止IFL的作用。与产生动作电位的细胞不同,IFL使假定的神经胶质细胞去极化,这与K⁺从丘脑皮质神经元外流一致。结果表明,一种渗漏K⁺通道介导了IFL诱导的丘脑中继神经元突触后膜电导增加。因此,如前一篇论文所报道的,IFL作用的单一非受体介导机制导致了电压依赖性Na⁺和Ca²⁺动作电位的超极化和电导分流。尽管麻醉药会影响各种神经系统,但仅丘脑皮质神经元中增强的K⁺渗漏就可能解释体内麻醉现象。

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