Wemer J, Schoffelmeer A N, Mulder A H
J Neurochem. 1982 Aug;39(2):349-56. doi: 10.1111/j.1471-4159.1982.tb03954.x.
The possible role of cyclic AMP in the presynaptic alpha-adrenoceptor-mediated modulation of [3H]noradrenaline (NA) release induced by 13 mM K+ from superfused rat cerebral cortex slices was investigated. Both dibutyryl-cyclic AMP (db-cAMP) and 8-bromo-cyclic AMP (8-Br-cAMP) dose-dependently (10(-4) - 10(-2) M) enhanced K+-induced (3H]NA release, maximally to about 160% of control. In contrast, db-cAMP had no effect on calcium-induced [3H]NA release in the presence of the calcium ionophore A 23187. Surprisingly, the phosphodiesterase (PDE) inhibitors 3-isobutyl-1-methylxanthine (IBMX). 7-benzyl-IBMX, 4-(3-cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidone (ZK 62771), and 4-(3-butoxy-4-methoxybenzyl)-2-imidazolidinone (Ro 20-1724) appeared to inhibit K+-induced [3H]NA release in a dose-dependent (10(-5) - 10(-3) M) manner. At a concentration of 10(-4) M, AK 62771 caused an inhibition of [3H]NA release by 30%, and this inhibitory effect was not affected by 10(-6) M phentolamine nor by 10(-3) M db-cAMP or 10(-4) M theophylline. Theophylline by itself enhanced [3H]NA release to about 135% of control. The inhibitor effect of the alpha-adrenoceptor agonist oxymetazoline (1 micro M) and the enhancing effect of the antagonist phentolamine (1 micro M) on [3H]NA release were significantly decreased in the presence of 10(-3) M db-cAMP or 8-Br-cAMP, whereas 10(-4) M ZK 62771 had no effect. In the presence of 10(-2) M NaF, a potent activator of adenylate cyclase, the inhibitory effect of oxymetazoline (1 micro M) on [3H]NA release was significantly decreased. The data obtained with the cyclic AMP analogues support the hypothesis that activation of presynaptic alpha-receptors modulating NA release results in an inhibition of a presynaptic adenylate cyclase. Possible causes for the anomalous effects of th PDE inhibitors are discussed.
研究了环磷酸腺苷(cAMP)在由13 mM钾离子诱导的、来自灌流大鼠大脑皮层切片的[3H]去甲肾上腺素(NA)释放的突触前α-肾上腺素能受体介导的调节中可能发挥的作用。二丁酰环磷酸腺苷(db-cAMP)和8-溴环磷酸腺苷(8-Br-cAMP)均呈剂量依赖性(10^(-4) - 10^(-2) M)地增强了钾离子诱导的[3H]NA释放,最大增强至对照的约160%。相比之下,在钙离子载体A 23187存在的情况下,db-cAMP对钙诱导的[3H]NA释放没有影响。令人惊讶的是,磷酸二酯酶(PDE)抑制剂3-异丁基-1-甲基黄嘌呤(IBMX)、7-苄基-IBMX、4-(3-环戊氧基-4-甲氧基苯基)-2-吡咯烷酮(ZK 62771)和4-(3-丁氧基-4-甲氧基苄基)-2-咪唑啉酮(Ro 20-1724)似乎以剂量依赖性(10^(-5) - 10^(-3) M)的方式抑制钾离子诱导的[3H]NA释放。在浓度为10^(-4) M时,ZK 62771导致[3H]NA释放抑制30%,并且这种抑制作用不受10^(-6) M酚妥拉明、10^(-3) M db-cAMP或10^(-4) M茶碱的影响。茶碱本身将[3H]NA释放增强至对照的约135%。在存在10^(-3) M db-cAMP或8-Br-cAMP的情况下,α-肾上腺素能受体激动剂氧甲唑啉(1 μM)对[3H]NA释放的抑制作用以及拮抗剂酚妥拉明(1 μM)对[3H]NA释放的增强作用均显著降低,而10^(-4) M ZK 62771没有影响。在存在10^(-2) M氟化钠(一种腺苷酸环化酶的强效激活剂)的情况下,氧甲唑啉(1 μM)对[3H]NA释放的抑制作用显著降低。使用环磷酸腺苷类似物获得的数据支持以下假设:调节NA释放的突触前α-受体的激活导致突触前腺苷酸环化酶的抑制。讨论了磷酸二酯酶抑制剂异常作用的可能原因。