Bogle R G, Moncada S, Pearson J D, Mann G E
Vascular Biology Research Centre, King's College, London.
Br J Pharmacol. 1992 Apr;105(4):768-70. doi: 10.1111/j.1476-5381.1992.tb09053.x.
The effects of inhibitors of nitric oxide (NO) synthase and other cationic amino acids on unidirectional L-arginine transport were studied in porcine aortic endothelial cells cultured in microwell plates or perfused in microcarrier columns. L-Homoarginine, L-lysine and L-ornithine inhibited transport of L-arginine. The NO synthase inhibitors NG-monomethyl-L-arginine and NG-iminoethyl-L-ornithine also reduced L-arginine uptake, whereas NG-nitro-L-arginine and its methyl-ester had no inhibitory effect. The ability to modulate selectively endothelial cell L-arginine transport or NO synthase activity will allow further characterization of the arginine transporter and its role in regulating NO biosynthesis.
在微孔板中培养或在微载体柱中灌注的猪主动脉内皮细胞中,研究了一氧化氮(NO)合酶抑制剂和其他阳离子氨基酸对单向L-精氨酸转运的影响。L-高精氨酸、L-赖氨酸和L-鸟氨酸抑制L-精氨酸的转运。NO合酶抑制剂NG-单甲基-L-精氨酸和NG-亚氨基乙基-L-鸟氨酸也降低了L-精氨酸的摄取,而NG-硝基-L-精氨酸及其甲酯没有抑制作用。选择性调节内皮细胞L-精氨酸转运或NO合酶活性的能力将有助于进一步表征精氨酸转运体及其在调节NO生物合成中的作用。