Tamaoki J, Kondo M, Sakai A, Tagaya E, Takemura H, Konno K
First Department of Medicine, Tokyo Women's Medical College, Japan.
Regul Pept. 1995 Dec 7;60(1):55-60. doi: 10.1016/0167-0115(95)00121-2.
We studied the effects of tachykinins on the generation of nitric oxide (NO) from canine cultured tracheal epithelial cells using a specific amperometric sensor for this molecule. Immersion of the NO-selective electrode in the medium bathing the cells detected the baseline current of 30.5-61.7 pA, which corresponded to NO concentration ([NO]) at 44.0 +/- 7.6 nM (mean +/- S.E.M.). Substance P (SP, 10(-6) M) increased the current from 51.3 +/- 9.8 to 73.6 +/- 11.4 pA (P < 0.001), an effect that was not affected by NG-nitro-D-arginine methylester, but inhibited by NG-nitro-L-arginine methylester by 83 +/- 9% (P < 0.001), and this inhibition was restored by the subsequent addition of L-arginine, but not by D-arginine. SP and neurokinin A (NKA) increased [NO] in a dose-dependent manner, the maximal increases from the baseline level being 71.0 +/- 14.9 and 33.4 +/- 8.5 nM, respectively (P < 0.001 for each), whereas neurokinin B (NKB) had no effect. In the presence of phosphoramidon, the response of each tachykinin was augmented, but the rank order of potency was still NKA > SP >> NKB. These results suggest that NO is spontaneously released from airway epithelium and that tachykinins stimulate epithelial NO generation via NK2 receptors.
我们使用针对该分子的特定安培传感器,研究了速激肽对犬培养气管上皮细胞一氧化氮(NO)生成的影响。将NO选择性电极浸入细胞培养液中,检测到基线电流为30.5 - 61.7 pA,这对应于44.0±7.6 nM(平均值±标准误)的NO浓度([NO])。P物质(SP,10⁻⁶ M)使电流从51.3±9.8 pA增加到73.6±11.4 pA(P < 0.001),该效应不受NG-硝基-D-精氨酸甲酯影响,但被NG-硝基-L-精氨酸甲酯抑制83±9%(P < 0.001),随后添加L-精氨酸可恢复这种抑制作用,而D-精氨酸则不能。SP和神经激肽A(NKA)以剂量依赖方式增加[NO],相对于基线水平的最大增加量分别为71.0±14.9和33.4±8.5 nM(各自P < 0.001),而神经激肽B(NKB)则无作用。在磷酰胺存在的情况下,每种速激肽的反应增强,但效力的排序仍为NKA > SP >> NKB。这些结果表明,NO从气道上皮细胞自发释放,并且速激肽通过NK2受体刺激上皮细胞生成NO。