Katsuragi T, Tokunaga T, Miyamoto K, Kuratomi L, Furukawa T
Department of Pharmacology, School of Medicine, Fukuoka University, Japan.
J Pharmacol Exp Ther. 1988 Oct;247(1):302-8.
Release of norepinephrine (NE) and ATP from the guinea pig vas deferens evoked by ouabain in combination with monensin or by high KCl was measured by a high-pressure liquid chromatography-ECD and luciferin-luciferase assay, respectively. Ouabain (10-100 microM) induced a concentration-dependent liberation of NE, which was enhanced by 10 microM monensin, a Na+-ionophore. The marked NE release elicited by the combined administration of both the drugs was unaffected by Ca++-removal but was reduced by lowering Na+ from the medium. This NE release in the Ca++-free medium was diminished markedly after treatment with 6-hydroxydopamine or reserpine and in low-temperature (25 degrees C) medium. This release was also decreased by ruthenium red (10-30 microM), an uptake inhibitor of Ca++ to mitochondria, and carbonyl cyanide-m-chlorophenyl hydrazone (10 microM), a metabolic inhibitor. On the other hand, 100 mM KCl caused a moderate, extracellular Ca++-dependent release of NE. ATP-outflow from the tissue evoked by 100 microM ouabain plus 10 microM monensin was almost unaltered by Ca++-removal but was inhibited by 6-hydroxydopamine or prazosin (0.3 microM), whereas release induced by high KCl was reduced by 6-hydroxydopamine and Ca++-free medium but was unaffected by prazosin. ATP/NE ratios at respective maximum effluxes evoked by 100 mM KCl and ouabain plus monensin were 6.59 and 0.22, respectively. These findings suggest that there may be more than one site of corelease for NE and ATP. Ouabain plus monensin seems to produce an extracellular Ca++-independent neuronal release of NE and ATP from the cytoplasmic and vesicular storage sites which predominantly release NE.(ABSTRACT TRUNCATED AT 250 WORDS)
分别通过高压液相色谱 - 电化学检测法和荧光素 - 荧光素酶测定法,测量哇巴因与莫能菌素联合作用或高钾氯化钾诱发的豚鼠输精管去甲肾上腺素(NE)和三磷酸腺苷(ATP)的释放。哇巴因(10 - 100微摩尔)诱导NE呈浓度依赖性释放,10微摩尔莫能菌素(一种钠离子载体)可增强这种释放。两种药物联合给药引起的显著NE释放不受去除钙离子的影响,但通过降低培养基中的钠离子浓度而减少。在无钙离子培养基中的这种NE释放在用6 - 羟基多巴胺或利血平处理后以及在低温(25摄氏度)培养基中明显减少。这种释放也被钌红(10 - 30微摩尔,一种钙离子向线粒体的摄取抑制剂)和羰基氰化物 - 间氯苯腙(10微摩尔,一种代谢抑制剂)降低。另一方面,100毫摩尔氯化钾引起适度的、细胞外钙离子依赖性NE释放。100微摩尔哇巴因加10微摩尔莫能菌素诱发的组织中ATP流出几乎不受去除钙离子的影响,但被6 - 羟基多巴胺或哌唑嗪(0.3微摩尔)抑制,而高钾氯化钾诱导的释放被6 - 羟基多巴胺和无钙离子培养基降低,但不受哌唑嗪影响。100毫摩尔氯化钾和哇巴因加莫能菌素诱发的各自最大流出量时的ATP/NE比值分别为6.59和0.22。这些发现表明,NE和ATP可能有不止一个共同释放位点。哇巴因加莫能菌素似乎从主要释放NE的细胞质和囊泡储存位点产生细胞外钙离子非依赖性的NE和ATP神经元释放。(摘要截短于250字)