Olson L M, Jacklet J W
J Neurosci. 1985 Dec;5(12):3214-27. doi: 10.1523/JNEUROSCI.05-12-03214.1985.
Each eye of Aplysia contains a population of electrically coupled pacemaker neurons whose synchronous activity can be recorded from the optic nerve as a compound action potential (CAP). The CAP frequency continues to show a circadian rhythm even when the eye is isolated from the animal and maintained in constant conditions, and thus it contains an autonomous circadian pacemaker, which may reside in the pacemaker neurons. The pacemaker neurons, along with retinal photoreceptors, send axons out of the optic nerve, which connects to the cerebral ganglion of the central nervous system (CNS). Pacemaker neurons, but not photoreceptors, may contain an aminergic transmitter, possibly dopamine (DA). We describe the central projections of optic nerve fibers using horseradish peroxidase filling of the cut optic nerve, and transport of radiolabeled macromolecules after selective exposure of the eye to [3H] leucine, which labels both pacemaker neurons and photoreceptors. We were able to determine the projections of pacemaker axons by exposing the eye to [3H]-3,4-dihydroxyphenylalanine [( 3H] DOPA and [3H]DA, which is preferentially taken up and transported by the pacemaker neurons. Pacemaker axons project bilaterally to the cerebral, pedal, and pleural ganglia and may extend as far as the abdominal ganglion. We corroborate this anatomical evidence by recording an orthodromic CAP in the optic nerve that had originated in the eye and subsequently recording the CAP in the CNS connectives and nerves that contained [3H]DOPA-labeled fibers. These results suggest that circadian pacemaker information from the eye is widely distributed throughout the CNS, including neural structures known from studies by others to mediate circadian-regulated behaviors, such as locomotion. Thus, Aplysia can now be used as a model system to examine the influence of the central projections of an identified circadian pacemaker on behavior, such as locomotion, at the level of identified central neurons.
海兔的每只眼睛都包含一群电耦合的起搏神经元,其同步活动可作为复合动作电位(CAP)从视神经记录下来。即使眼睛与动物分离并在恒定条件下维持,CAP频率仍会呈现昼夜节律,因此它包含一个自主的昼夜节律起搏器,可能存在于起搏神经元中。起搏神经元与视网膜光感受器一起,将轴突送出视神经,视神经连接到中枢神经系统(CNS)的脑神经节。起搏神经元而非光感受器可能含有一种胺能递质,可能是多巴胺(DA)。我们使用辣根过氧化物酶填充切断的视神经,并在眼睛选择性暴露于[3H]亮氨酸后运输放射性标记的大分子来描述视神经纤维的中枢投射,[3H]亮氨酸可标记起搏神经元和光感受器。通过将眼睛暴露于[3H]-3,4-二羟基苯丙氨酸[(3H)多巴]和[3H]DA,我们能够确定起搏轴突的投射,[3H]DA优先被起搏神经元摄取和运输。起搏轴突双侧投射到脑、足和胸膜神经节,甚至可能延伸到腹神经节。我们通过记录起源于眼睛的视神经中的顺向CAP,随后在包含[3H]多巴标记纤维的CNS连接和神经中记录CAP,来证实这一解剖学证据。这些结果表明,来自眼睛的昼夜节律起搏器信息广泛分布于整个CNS,包括其他研究已知的介导昼夜节律调节行为(如运动)的神经结构。因此,海兔现在可作为一个模型系统,用于在已确定的中枢神经元水平上研究已确定的昼夜节律起搏器的中枢投射对行为(如运动)的影响。