Ying Shui-Wang, Goldstein Peter A
C.V. Starr Laboratory for Molecular Neuropharmacology, Deptartment of Anesthesiology A-1050, Weill Medical College, Cornell University, 1300 York Ave., New York, NY 10021, USA.
J Neurophysiol. 2005 Apr;93(4):1935-48. doi: 10.1152/jn.01058.2004. Epub 2004 Nov 24.
The GABAergic reticular thalamic nucleus (RTN) is a major source of inhibition for thalamocortical neurons in the ventrobasal complex (VB). Thalamic circuits are thought to be an important anatomic target for general anesthetics. We investigated presynaptic actions of the intravenous anesthetic propofol in RTN neurons, using RTN-retained and RTN-removed brain slices. In RTN-retained slices, focal and bath application of propofol increased intrinsic excitability, temporal summation, and spike firing rate in RTN neurons. Propofol-induced activation was associated with suppression of medium afterhyperpolarization potentials. This activation was mimicked and completely occluded by the small conductance calcium-activated potassium (SK) channel blocker apamin, indicating that propofol could enhance RTN excitability by blocking SK channels. Propofol increased GABAergic transmission at RTN-VB synapses, consistent with excitation of presynaptic RTN neurons. Stimulation of RTN resulted in synaptic inhibition in postsynaptic neurons in VB, and this inhibition was potentiated by propofol in a concentration-dependent manner. Removal of RTN resulted in a dramatic reduction of both spontaneous postsynaptic inhibitory current frequency and propofol-mediated inhibition of VB neurons. Thus the existence and activation of RTN input were essential for propofol to elicit thalamocortical suppression; such suppression resulted from shunting through the postsynaptic GABA(A) receptor-mediated chloride conductance. The results indicate that propofol enhancement of RTN-mediated inhibitory input via blockade of SK channels may play a critical role in "gating" spike firing in thalamocortical relay neurons.
γ-氨基丁酸能网状丘脑核(RTN)是腹侧基底复合体(VB)中丘脑皮质神经元的主要抑制来源。丘脑环路被认为是全身麻醉药的一个重要解剖学靶点。我们使用保留RTN和去除RTN的脑片,研究了静脉麻醉药丙泊酚在RTN神经元中的突触前作用。在保留RTN的脑片中,局部和浴槽应用丙泊酚可增加RTN神经元的内在兴奋性、时间总和及放电频率。丙泊酚诱导的激活与中等后超极化电位的抑制有关。小电导钙激活钾(SK)通道阻断剂蜂毒明肽可模拟并完全阻断这种激活,表明丙泊酚可通过阻断SK通道增强RTN的兴奋性。丙泊酚增加了RTN-VB突触处的γ-氨基丁酸能传递,这与突触前RTN神经元的兴奋一致。刺激RTN可导致VB中突触后神经元的突触抑制,丙泊酚以浓度依赖的方式增强这种抑制。去除RTN可导致自发性突触后抑制电流频率和丙泊酚介导的VB神经元抑制均显著降低。因此,RTN输入的存在和激活是丙泊酚引发丘脑皮质抑制所必需的;这种抑制是通过突触后γ-氨基丁酸A(GABA(A))受体介导的氯电导分流产生的。结果表明,丙泊酚通过阻断SK通道增强RTN介导的抑制性输入可能在丘脑皮质中继神经元的“门控”放电中起关键作用。