Yamada J, Sugimoto Y, Yoshikawa T, Horisaka K
Department of Pharmacology, Kobe Pharmaceutical University, Japan.
Neuroreport. 1997 Jul 7;8(9-10):2097-100. doi: 10.1097/00001756-199707070-00002.
The effects of a nitric oxide (NO) synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME) on 2-deoxy-D-glucose (2-DG)-induced hyperphagia were investigated in rats. L-NAME dose-dependently inhibited 2-DG-induced eating in non-food-deprived rats, although the inactive isomer D-NAME on 2-DG-induced hyperphagia were inhibited by co-administration of L-arginine. The neuronal NO synthase inhibitor 7-nitroindazole also inhibited 2-DG-induced hyperphagia. These results suggest that 2-DG-induced hyperphagia is linked with NO and that brain NO may participate in this hyperphagic model.
研究了一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸甲酯(L-NAME)对大鼠2-脱氧-D-葡萄糖(2-DG)诱导的摄食亢进的影响。L-NAME剂量依赖性地抑制未禁食大鼠中2-DG诱导的进食,尽管无活性的异构体D-NAME对2-DG诱导的摄食亢进的抑制作用可通过共同给予L-精氨酸而被阻断。神经元型NO合酶抑制剂7-硝基吲唑也抑制2-DG诱导的摄食亢进。这些结果表明,2-DG诱导的摄食亢进与NO有关,并且脑内的NO可能参与了这种摄食亢进模型。