Shintani F, Kanba S, Nakaki T, Nakamura R, Sato K, Yagi G, Richelson E, Kato R, Asai M
Department of Neuro-psychiatry, Keio University School of Medicine, Tokyo, Japan.
Neuropsychopharmacology. 1994 Oct;11(2):119-24. doi: 10.1038/npp.1994.41.
We investigated the effects of lithium ion (Li+) on muscarinic receptor-mediated nitric oxide (NO) generation, and guanylate cyclase (GCase) activation using the mouse neuroblastoma clone, N1E-115. The levels of released NO were determined by measuring the levels of nitrite/nitrate in the incubation medium, and the activity of GCase was measured with an assay for cellular cyclic [3H] GMP levels. We determined that Li+ had no effects on muscarinic receptor-activated elevation of nitrite/nitrate levels, which were significantly inhibited by 100 microM L-NG-monomethylarginine, although it has been reported that Li+ inhibits muscarinic receptor-activated cyclic GMP formation in the cells. In addition, Li+ inhibited the cyclic GMP formation induced by an NO donor, sodium nitroprusside (SNP), in both intact cells and a crude cellular homogenate; thus, the inhibition by Li+ of muscarinic receptor-mediated cyclic GMP synthesis appeared to be at the level of GCase, but not NO synthase.
我们使用小鼠神经母细胞瘤克隆N1E-115研究了锂离子(Li+)对毒蕈碱受体介导的一氧化氮(NO)生成以及鸟苷酸环化酶(GCase)激活的影响。通过测量孵育培养基中亚硝酸盐/硝酸盐的水平来确定释放的NO水平,并用细胞环[3H]GMP水平测定法测量GCase的活性。我们确定Li+对毒蕈碱受体激活引起的亚硝酸盐/硝酸盐水平升高没有影响,100 microM L-NG-单甲基精氨酸可显著抑制该升高,尽管有报道称Li+可抑制细胞中毒蕈碱受体激活的环GMP形成。此外,Li+在完整细胞和粗制细胞匀浆中均抑制了由NO供体硝普钠(SNP)诱导的环GMP形成;因此,Li+对毒蕈碱受体介导的环GMP合成的抑制似乎发生在GCase水平,而非一氧化氮合酶水平。