Wellard J W, Miethke P, Morgan I G
Centre for Visual Sciences and Research School of Biological Sciences, Australian National University.
Neurosci Lett. 1995 Dec 1;201(1):17-20. doi: 10.1016/0304-3940(94)12120-f.
Nitric oxide synthase (NOS) activity, as measured by the formation of L-[3H]citrulline from L-[3H]arginine, was blocked by micromolar concentrations of NOS inhibitors in retinal homogenates, but concentrations approximately 20-3000 times higher were needed in intact retina. The higher concentrations could be related to transport of the NOS inhibitors into neuronal cells and/or their sequestration within glial cells. NG-monomethyl-L-arginine and N-iminoethyl-L-ornithine significantly inhibited L-[3H]arginine uptake, whereas N omega-nitro-L-arginine methyl ester and N omega-nitro-L-arginine had little or no effect on L-[3H]arginine uptake. The high concentrations of the inhibitors needed to inhibit nitric oxide production in intact tissue and their different interactions with arginine uptake systems may explain some of the conflicting results on the activity of NOS inhibitors on a range of physiological parameters in vivo.
通过L-[3H]精氨酸生成L-[3H]瓜氨酸来测定的一氧化氮合酶(NOS)活性,在视网膜匀浆中被微摩尔浓度的NOS抑制剂所阻断,但在完整视网膜中则需要大约高20 - 3000倍的浓度。较高的浓度可能与NOS抑制剂向神经元细胞的转运和/或它们在神经胶质细胞内的隔离有关。NG-单甲基-L-精氨酸和N-亚氨基乙基-L-鸟氨酸显著抑制L-[3H]精氨酸的摄取,而Nω-硝基-L-精氨酸甲酯和Nω-硝基-L-精氨酸对L-[3H]精氨酸摄取几乎没有影响。在完整组织中抑制一氧化氮产生所需的高浓度抑制剂以及它们与精氨酸摄取系统的不同相互作用,可能解释了关于NOS抑制剂在一系列体内生理参数上的活性的一些相互矛盾的结果。