Nowak Lionel G, Rosay Benoît, Czégé Dávid, Fonta Caroline
Centre de Recherche Cerveau et Cognition (CerCo), Université de Toulouse UPS; CNRS UMR 5549 , Toulouse, France,
Subcell Biochem. 2015;76:239-81. doi: 10.1007/978-94-017-7197-9_12.
Tissue non-specific alkaline phosphatase (TNAP) may be involved in the synthesis of GABA and adenosine, which are the main inhibitory neurotransmitters in cortex. We explored this putative TNAP function through electrophysiological recording (local field potential ) in slices of mouse somatosensory cortex maintained in vitro. We used tetramisole, a well documented TNAP inhibitor, to block TNAP activity. We expected that inhibiting TNAP with tetramisole would lead to an increase of neuronal response amplitude, owing to a diminished availability of GABA and/or adenosine. Instead, we found that tetramisole reduced neuronal response amplitude in a dose-dependent manner. Tetramisole also decreased axonal conduction velocity. Levamisole had identical effects. Several control experiments demonstrated that these actions of tetramisole were independent from this compound acting on TNAP. In particular, tetramisole effects were not stereo-specific and they were not mimicked by another inhibitor of TNAP, MLS-0038949. The decrease of axonal conduction velocity and preliminary intracellular data suggest that tetramisole blocks voltage-dependent sodium channels. Our results imply that levamisole or tetramisole should not be used with the sole purpose of inhibiting TNAP in living excitable cells as it will also block all processes that are activity-dependent. Our data and a review of the literature indicate that tetramisole may have at least four different targets in the nervous system. We discuss these results with respect to the neurological side effects that were observed when levamisole and tetramisole were used for medical purposes, and that may recur nowadays due to the recent use of levamisole and tetramisole as cocaine adulterants.
组织非特异性碱性磷酸酶(TNAP)可能参与γ-氨基丁酸(GABA)和腺苷的合成,而这两种物质是皮质中主要的抑制性神经递质。我们通过在体外维持的小鼠体感皮质切片中进行电生理记录(局部场电位)来探究TNAP的这一假定功能。我们使用了四咪唑,一种有充分文献记载的TNAP抑制剂,来阻断TNAP活性。我们预期,用四咪唑抑制TNAP会由于GABA和/或腺苷的可用性降低而导致神经元反应幅度增加。然而,我们发现四咪唑以剂量依赖的方式降低了神经元反应幅度。四咪唑还降低了轴突传导速度。左旋咪唑也有相同的作用。多项对照实验表明,四咪唑的这些作用独立于该化合物对TNAP的作用。特别是,四咪唑的作用不是立体特异性的,且另一种TNAP抑制剂MLS-0038949并不能模拟其作用。轴突传导速度的降低以及初步的细胞内数据表明,四咪唑阻断了电压依赖性钠通道。我们的结果表明,左旋咪唑或四咪唑不应用于仅抑制活的可兴奋细胞中TNAP的唯一目的,因为它还会阻断所有依赖于活性的过程。我们的数据以及对文献的综述表明,四咪唑在神经系统中可能至少有四个不同的靶点。我们结合左旋咪唑和四咪唑用于医疗目的时观察到的神经副作用来讨论这些结果,并且由于最近将左旋咪唑和四咪唑用作可卡因掺杂物,这些副作用如今可能会再次出现。