Otten U, Mueller R A, Oesch F, Thoenen H
Proc Natl Acad Sci U S A. 1974 Jun;71(6):2217-21. doi: 10.1073/pnas.71.6.2217.
To decide whether adenosine 3':5'-cyclic monophosphate (cyclic AMP) plays a role as a second messenger in the trans-synaptic induction of tyrosine 3-monooxygenase (EC 1.14.16.2), it is desirable to discriminate between neuronal and extraneuronal changes in cyclic AMP concentration. Treatment of newborn rats with nerve growth factor antiserum or 6-hydroxydopamine, leading to destruction of 61-85% of the adrenergic nerve cell bodies in the superior cervical ganglion, led to a decrease in cyclic AMP of only 16-28%. This observation demonstrates that a relatively small portion of cyclic AMP is localized in the adrenergic neurons. However, administration of isoproterenol produced an increase (12-fold) in cyclic AMP only in this neuronal pool. Neither single nor repeated injections of isoproterenol led to induction of tyrosine monoxygenase. This, together with previous observations that experimental conditions leading to induction of the enzyme do not produce significant increases of cyclic AMP in the whole ganglion, is taken as an indication that cyclic AMP is not acting as a second messenger in the trans-synaptic induction of tyrosine monooxygenase in the rat superior cervical ganglion. In the rat adrenal medulla, treatment with reserpine led to both a shortlasting (60-90 min) increase in cyclic AMP and a subsequent induction of tyrosine monooxygenase. However, the increase in cyclic AMP was almost completely prevented (40 compared to 320%) by pretreatment of the rats with propranolol while the induction of tyrosine monooxygenase was not diminished. This observation also argues against an exclusive key-function of cyclic AMP in trans-synaptic induction of tyrosine monooxygenase in the adrenal medulla.
为了确定3':5'-环磷酸腺苷(环磷腺苷)是否作为酪氨酸3-单加氧酶(EC 1.14.16.2)跨突触诱导过程中的第二信使发挥作用,需要区分环磷腺苷浓度在神经元和神经元外的变化。用神经生长因子抗血清或6-羟基多巴胺处理新生大鼠,导致颈上神经节中61-85%的肾上腺素能神经细胞体被破坏,仅使环磷腺苷减少了16-28%。这一观察结果表明,相对较小部分的环磷腺苷定位于肾上腺素能神经元中。然而,异丙肾上腺素的给药仅在这个神经元池中使环磷腺苷增加了12倍。单次或重复注射异丙肾上腺素均未导致酪氨酸单加氧酶的诱导。这一点,连同先前的观察结果,即导致该酶诱导的实验条件不会使整个神经节中的环磷腺苷显著增加,被视为环磷腺苷在大鼠颈上神经节酪氨酸单加氧酶的跨突触诱导中不作为第二信使发挥作用的一个迹象。在大鼠肾上腺髓质中,利血平处理导致环磷腺苷短暂增加(60-90分钟),随后诱导酪氨酸单加氧酶。然而,在用普萘洛尔预处理大鼠后,环磷腺苷的增加几乎完全被阻止(从320%降至40%),而酪氨酸单加氧酶的诱导并未减弱。这一观察结果也反对环磷腺苷在肾上腺髓质酪氨酸单加氧酶跨突触诱导中具有唯一关键作用的观点。