Cedar H, Schwartz J H
J Gen Physiol. 1972 Nov;60(5):570-87. doi: 10.1085/jgp.60.5.570.
Serotonin and dopamine, both likely transmitter substances in Aplysia, stimulated formation of adenosine-3',5' monophosphate (cAMP) in ganglia, connectives, and identified nerve cell bodies. This widespread distribution suggests that receptors for the response are localized throughout the nervous system, as is adenyl cyclase. Both synthesis of cAMP-(3)H from precursor previously labeled in incubations with adenine-(3)H and total content of cAMP were stimulated up to 15-fold. The acetylcholine analogue carbachol, glutamate, norepinephrine, and histamine were inactive. Full stimulation occurred within 2-4 min of applying serotonin; the extent of the effect was half maximal at 6micro serotonin. Even in the continued presence of serotonin, the increased cAMP diminished with time. When serotonin was removed, tissue remained refractory for 15-20 min; sensitivity returned after 25 min. Serotonin stimulated cAMP after removal of extracellular Na, K, or Cl and in isotonic sucrose, with all extracellular ions removed. Elevating Mg, which blocked the stimulation of cAMP caused by synaptic activity, did not affect the response to serotonin. Thus the response appeared to be independent of transmitter release and of changes in synaptic potentials and current flow. The role of cAMP in neuronal functioning remains to be determined. Conditions which markedly increased cAMP in neurons, however, did not affect the rate of RNA synthesis, nor did they alter the distribution of phosphorylated adenine or uridine nucleotides.
血清素和多巴胺可能都是海兔体内的递质,它们能刺激神经节、神经索和已鉴定的神经细胞体中3',5'-环磷酸腺苷(cAMP)的形成。这种广泛的分布表明,该反应的受体在整个神经系统中都有定位,腺苷酸环化酶也是如此。用腺嘌呤-(3)H预标记的前体合成cAMP-(3)H以及cAMP的总含量都被刺激了15倍之多。乙酰胆碱类似物卡巴胆碱、谷氨酸、去甲肾上腺素和组胺则无活性。施加血清素后2 - 4分钟内出现完全刺激;在6微摩尔血清素时,效应程度达到最大值的一半。即使血清素持续存在,cAMP的增加也会随时间减少。去除血清素后,组织在15 - 20分钟内仍处于不应期;25分钟后敏感性恢复。在去除细胞外的钠、钾或氯以及所有细胞外离子的等渗蔗糖溶液中,血清素仍能刺激cAMP的产生。提高镁离子浓度可阻断突触活动引起的cAMP刺激,但不影响对血清素的反应。因此,该反应似乎与递质释放以及突触电位和电流的变化无关。cAMP在神经元功能中的作用仍有待确定。然而,显著增加神经元中cAMP的条件既不影响RNA合成速率,也不改变磷酸化腺嘌呤或尿嘧啶核苷酸的分布。