Peterlin Zita, Ishizawa Yumiko, Araneda Ricardo, Eckenhoff Roderic, Firestein Stuart
Department of Biological Sciences, Columbia University, 920 Fairchild-MC#2439, 1212 Amsterdam Ave., New York, NY 10027, USA.
Mol Cell Neurosci. 2005 Dec;30(4):506-12. doi: 10.1016/j.mcn.2005.08.012. Epub 2005 Sep 26.
Ion channels and ionotropic neurotransmitter receptors have long been investigated as the principle targets of inhaled volatile anesthetics (VAs), but emerging evidence suggests that G-protein coupled receptors (GPCRs) might also directly interact with VAs. To survey the extent of interaction between VAs and diverse GPCRs, we have turned to the 1000+ member family of olfactory receptors (ORs), taking advantage of their unique expression pattern of a single OR per neuron. Through optical imaging and electrophysiological recordings, we show that different VAs trigger the normal transduction cascade in distinct subsets of cells in a dose-dependant manner. Together with evidence of antagonism by odorants, this selective activation strongly implicates a direct action of VAs upon particular olfactory receptors. The finding that VAs stimulate nearly 8% of olfactory GPCRs suggests that probing related Class A GPCRs may reveal a pool of VA targets whose altered signaling contributes to anesthetic effects.
离子通道和离子型神经递质受体长期以来一直被作为吸入性挥发性麻醉剂(VAs)的主要作用靶点进行研究,但新出现的证据表明,G蛋白偶联受体(GPCRs)也可能与VAs直接相互作用。为了探究VAs与多种GPCRs之间的相互作用程度,我们借助嗅觉受体(ORs)这个拥有1000多个成员的家族,利用其每个神经元仅表达一种OR的独特表达模式展开研究。通过光学成像和电生理记录,我们发现不同的VAs以剂量依赖的方式在不同的细胞亚群中触发正常的转导级联反应。结合气味剂拮抗作用的证据,这种选择性激活强烈表明VAs对特定嗅觉受体有直接作用。VAs能刺激近8%的嗅觉GPCRs这一发现表明,探究相关的A类GPCRs可能会揭示出一批VA作用靶点,其信号改变会导致麻醉效果。