Murphy S, Simmons M L, Agullo L, Garcia A, Feinstein D L, Galea E, Reis D J, Minc-Golomb D, Schwartz J P
Dept of Pharmacology, University of Iowa College of Medicine, Iowa City 52242.
Trends Neurosci. 1993 Aug;16(8):323-8. doi: 10.1016/0166-2236(93)90109-y.
Attention has focused on particular neurons as the source of nitric oxide (NO) within the parenchyma of the CNS. In contrast, glial cells have been viewed mainly as potential reservoirs of L-arginine, the substrate for nitric oxide synthase (NOS), and as likely targets for neuronally derived NO because of their proximity and their expression of soluble guanylyl cyclase (sGC). However, it is becoming evident that astrocytes display both constitutive and inducible NOS activity under various conditions, and that activated microglia express an inducible NOS. The NO-producing capacity of oligodendrocytes is not yet known. Glial-derived NO has significant implications for CNS pathophysiology, given the anatomical location and abundance of these cells, and the wide variety of potential interactions that NO can have with cellular biochemistry. Our intention here is to evaluate the evidence for NO production from non-neuronal CNS sources and thus prompt discussion about potential 'nitrinergic' roles for glial cells.
人们已将注意力集中于特定神经元,视其为中枢神经系统实质内一氧化氮(NO)的来源。相比之下,神经胶质细胞主要被视为一氧化氮合酶(NOS)底物L-精氨酸的潜在储存库,并且由于其与神经元的接近程度以及可溶性鸟苷酸环化酶(sGC)的表达,它们可能是神经元衍生的NO的作用靶点。然而,越来越明显的是,星形胶质细胞在各种条件下都表现出组成型和诱导型NOS活性,并且活化的小胶质细胞表达诱导型NOS。少突胶质细胞产生NO的能力尚不清楚。鉴于这些细胞的解剖位置和数量,以及NO与细胞生物化学可能存在的广泛相互作用,神经胶质细胞衍生的NO对中枢神经系统病理生理学具有重要意义。我们的目的是评估中枢神经系统非神经元来源产生NO的证据,从而引发关于神经胶质细胞潜在“硝能”作用的讨论。