Bierman Hilary S, Schriefer Julie E, Zottoli Steven J, Hale Melina E
Committee on Neurobiology, University of Chicago, Chicago, IL 60637, USA.
J Exp Biol. 2004 Oct;207(Pt 22):3985-97. doi: 10.1242/jeb.01228.
While most actinopterygian fishes perform C-start or S-start behaviors as their primary startle responses, many elongate species instead use a withdrawal movement. Studies of withdrawal have focused on the response to head-directed or nonspecific stimuli. During withdrawal, the animal moves its head back from the stimulus, often resulting in several tight bends in the body. In contrast to C-start or S-start behaviors, withdrawal to a head stimulus generally does not involve a subsequent propulsive stage of movement. We examined intraspecific diversity in withdrawal behavior and muscle activity patterns of the rope fish, Erpetoichthys calabaricus, in response to stimulation of the head and the tail. In addition, we describe the anatomy of the Mauthner cells and their axon caps, structures that are generally absent in species with a withdrawal startle. We recorded high-speed video (250 Hz) and electromyograms (EMGs) from 12 electrodes in the axial muscle during the behavioral response. We used Bodian silver staining techniques to visualize Mauthner cell and axon cap morphology. We found that E. calabaricus responds with a withdrawal to both head and tail stimulation. Tail stimulation elicits a stronger kinematic and muscle activity response than head stimulation. While withdrawal movement generally constitutes the entire response to head stimuli, withdrawal was followed by propulsive movements when the tail was stimulated, suggesting that withdrawal can both act alone and serve as the first stage of a propulsive startle. Unexpectedly, bilaterality of muscle activity was variable for responses to both head and tail stimuli. In addition, we were surprised to find that E. calabaricus has a distinct axon cap associated with its Mauthner cell. These data suggest that the withdrawal response is a more diverse functional system than has previously been believed.
虽然大多数硬骨鱼将C型启动或S型启动行为作为其主要的惊吓反应,但许多细长型物种则采用退缩运动。对退缩运动的研究主要集中在对头部定向或非特异性刺激的反应上。在退缩过程中,动物会将头部从刺激源移开,身体通常会出现几个紧密的弯曲。与C型启动或S型启动行为不同,对头部刺激的退缩通常不涉及随后的推进运动阶段。我们研究了绳纹鱼(Erpetoichthys calabaricus)在对头部和尾部刺激的反应中,退缩行为和肌肉活动模式的种内多样性。此外,我们描述了Mauthner细胞及其轴突帽的解剖结构,这些结构在具有退缩惊吓反应的物种中通常不存在。我们在行为反应期间,从轴向肌肉中的12个电极记录了高速视频(250 Hz)和肌电图(EMG)。我们使用Bodian银染技术来观察Mauthner细胞和轴突帽的形态。我们发现,绳纹鱼对头部和尾部刺激均以退缩反应。尾部刺激引发的运动学和肌肉活动反应比头部刺激更强。虽然退缩运动通常构成对头部刺激的整个反应,但当尾部受到刺激时,退缩之后会出现推进运动,这表明退缩既可以单独起作用,也可以作为推进惊吓的第一阶段。出乎意料的是,对头部和尾部刺激的反应中,肌肉活动的双侧性是可变的。此外,我们惊讶地发现,绳纹鱼的Mauthner细胞有一个独特的轴突帽。这些数据表明,退缩反应是一个比以前认为的更加多样化的功能系统。