Wainwright Marcy L, Zhang Han, Byrne John H, Cleary Leonard J
W. M. Keck Center for the Neurobiology of Learning and Memory, Department of Neurobiology and Anatomy, University of Texas-Houston Medical School, Houston, Texas 77030, USA.
J Neurosci. 2002 May 15;22(10):4132-41. doi: 10.1523/JNEUROSCI.22-10-04132.2002.
Biophysical, biochemical, and morphological studies have implicated sensory neurons as key sites of plasticity in the formation and retention of the memory of long-term sensitization in Aplysia californica. This study examined the effects of different sensitization training protocols on the structure of sensory neurons mediating the tail-siphon withdrawal reflex. A 4 d training period produced a robust localized outgrowth in these sensory neurons observed 24 hr after the end of training. These changes are consistent with previous results in siphon sensory neurons (Bailey and Chen, 1988a). In contrast, 1 d of sensitization training, which has been shown to effectively induce long-term behavioral sensitization and synaptic facilitation (Frost et al., 1985; Cleary et al., 1998), is not associated with morphological changes in tail sensory neurons at either 24 hr or 4 d after training. Similarly, a single treatment with the growth factor TGF-beta, which also induced facilitation, did not alter sensory neuron morphology. The different effectiveness of the two protocols was not simply a reflection of the number of stimuli presented, because a 1 d massed training protocol did not produce sensitization 24 hr after training, nor did it induce neuronal outgrowth. These results suggest that extensive sensitization training is required to induce neuronal outgrowth in tail sensory neurons, indicating that the memory of long-term sensitization induced by 1 d of training is mechanistically different from that induced by 4 d of training. Moreover, the induction of a form of long-term sensitization associated with neuronal outgrowth does not appear to be a function of the amount of stimulation but does appear to be dependent on the temporal spacing of the stimulation over multiple days.
生物物理学、生物化学和形态学研究表明,感觉神经元是加州海兔长期敏感化记忆形成和保留过程中可塑性的关键位点。本研究考察了不同的敏感化训练方案对介导尾-虹吸管撤离反射的感觉神经元结构的影响。为期4天的训练期在训练结束24小时后,使这些感觉神经元出现了强烈的局部生长。这些变化与之前在虹吸管感觉神经元中的研究结果一致(贝利和陈,1988a)。相反,已被证明能有效诱导长期行为敏感化和突触易化的1天敏感化训练(弗罗斯特等人,1985;克利里等人,1998),在训练后24小时或4天时,与尾感觉神经元的形态变化无关。同样,单一使用生长因子转化生长因子-β进行处理,虽然也能诱导易化,但并未改变感觉神经元的形态。这两种方案效果不同,并非仅仅反映了所施加刺激的数量,因为1天的集中训练方案在训练后24小时并未产生敏感化,也未诱导神经元生长。这些结果表明,需要进行广泛的敏感化训练才能诱导尾感觉神经元生长,这表明1天训练诱导的长期敏感化记忆与4天训练诱导的记忆在机制上有所不同。此外,与神经元生长相关的一种长期敏感化形式的诱导似乎不是刺激量的函数,但似乎确实取决于多天刺激的时间间隔。