Crow Terry, Tian Lian-Ming
Department of Neurobiology and Anatomy, University of Texas Medical School, Houston, Texas 77030, USA.
Learn Mem. 2003 May-Jun;10(3):209-16. doi: 10.1101/lm.58603.
Pavlovian conditioning in Hermissenda consists of pairing light, the conditioned stimulus (CS) with activation of statocyst hair cells, the unconditioned stimulus (US). Conditioning produces CS-elicited foot shortening and inhibition of light-elicited locomotion, the two conditioned responses (CRs). Conditioning correlates have been identified in the primary sensory neurons (photoreceptors) of the CS pathway, interneurons that receive monosynaptic input from identified photoreceptors, and putative pedal motor neurons. While cellular mechanisms of acquisition produced by the synaptic interaction between the CS and US pathways are well-documented, little is known about the mechanisms responsible for the generation or expression of the CR. Here we show that in conditioned animals light reduced tonic firing of ciliary activating pedal neurons (VP1) below their pre-CS baseline levels. In contrast, pseudorandom controls expressed a significant increase in CS-elicited tonic firing of VP1 as compared to pre-CS baseline activity. Identified interneurons in the visual pathway that have established polysynaptic connections with VP1 were examined in conditioned animals and pseudorandom controls. Depolarization of identified type Ie interneurons with extrinsic current elicited a significant increase in IPSPs recorded in VP1 pedal neurons of conditioned animals as compared with pseudorandom controls. Conditioning also enhanced intrinsic excitability of type Ie interneurons of conditioned animals as compared to pseudorandom controls. Light evoked a modest increase in IPSP frequency in VP1 of conditioned preparations and a significant decrease in IPSP frequency in VP1 of pseudorandom controls. Our results show that a combination of synaptic facilitation and intrinsic enhanced excitability in identified components of the CS pathway may explain light-elicited inhibition of locomotion in conditioned animals.
在海兔(Hermissenda)中,经典条件作用包括将光(条件刺激,CS)与平衡囊毛细胞的激活(非条件刺激,US)配对。条件作用会产生CS诱发的足部缩短以及对光诱发运动的抑制,这两种是条件反应(CRs)。在CS通路的初级感觉神经元(光感受器)、接受来自特定光感受器单突触输入的中间神经元以及假定的踏板运动神经元中已经确定了条件作用相关因素。虽然CS和US通路之间的突触相互作用所产生的习得细胞机制已有充分记录,但对于负责CR产生或表达的机制却知之甚少。在这里,我们表明,在经过条件作用的动物中,光使睫状激活踏板神经元(VP1)的紧张性放电低于其CS前基线水平。相比之下,与CS前基线活动相比,伪随机对照组中CS诱发的VP1紧张性放电显著增加。在经过条件作用的动物和伪随机对照组中,检查了在视觉通路中已与VP1建立多突触连接的特定中间神经元。与伪随机对照组相比,用外部电流使特定的Ie型中间神经元去极化,在经过条件作用的动物的VP1踏板神经元中记录到的抑制性突触后电位(IPSPs)显著增加。与伪随机对照组相比,条件作用还增强了经过条件作用的动物的Ie型中间神经元的内在兴奋性。光在经过条件作用的制剂的VP1中诱发IPSP频率适度增加,而在伪随机对照组的VP1中诱发IPSP频率显著降低。我们的结果表明,CS通路特定成分中的突触易化和内在兴奋性增强相结合,可能解释了在经过条件作用的动物中光诱发的运动抑制。