Physiological Laboratory of Rutgers College, New Brunswick, N. J., and the Marine Biological Laboratory, Woods Hole, Mass.
J Gen Physiol. 1920 Mar 20;2(4):319-24. doi: 10.1085/jgp.2.4.319.
From what has been said concerning the neuromuscular organization of the Asterias ray, it is possible to arrive at certain definite conclusions regarding the nature of the stereotropism of that organ. The righting movements from the start are not haphazard; i.e., they cannot be explained on any hypothesis of "trial and error." The excitation of the sensory cells of the dorsal sheath initiates dorsal flexure of the ray. This movement makes it possible for the tube feet of the tip to touch bottom and start the vigorous action which follows and completes the righting If the "feelers" by chance touch bottom they initiate the reaction de novo. As to the remaining phases, the stereotropic reaction of the ray is referable to the high degree of surface sensitivity of the tube feet disks and the propagation of excitatory and inhibitory impulses, resulting from stimulation, along appropriate paths to the muscles of the ray. In this respect the tube feet may be regarded as playing a role similar to that of tropistic receptors in general. That is, unequal stimulation of the receptors causes a corresponding inequality of tone or of contraction in the musculature which ultimately results in an equilibrium of orientation to the factor involved. It is evident that as a mechanism for righting stereotropism differs in one important respect from other tropisms. The latter depend for their operation upon unilateral effects in organisms which are dynamically bilaterally symmetrical. In stereotropism the sensitivity of the organism is not distributed in bilaterally symmetrical fashion. As a rule only the ventral side is stereosensitive; i.e., the sensitivity is unilaterally distributed. There is a tropistic action in such cases because of the fact that when the sensitive surface is only partially stimulated an unequal contraction of the musculature follows and this as a result brings the sensitive surface into such a position that it is all equally stimulated. Equal muscle tone follows and the organism is in equilibrium with its environment.
从星鱼的神经肌肉组织的论述中,我们可以对该器官的向性本质得出某些明确的结论。最初的翻身运动并非偶然发生的;也就是说,不能根据“尝试和错误”假说对其进行解释。背甲感觉细胞的兴奋会引发星鱼的背侧弯曲。这种运动使触须尖端的管足能够触底,并开始随后的强烈运动,从而完成翻身。如果“触角”偶然触底,它们会重新开始反应。至于其余阶段,星鱼的向性反应归因于管足盘的高度表面敏感性,以及由于刺激而沿适当路径传播到星鱼肌肉的兴奋性和抑制性冲动。在这方面,可以认为管足起着与一般向性受体相似的作用。也就是说,受体的不等刺激会导致肌肉张力或收缩的相应不等,最终导致对所涉及因素的定向平衡。显然,作为一种翻身向性机制,它在一个重要方面与其他向性不同。后者依赖于生物体中动态双侧对称的单侧效应。在向性中,生物体的敏感性不是以双侧对称的方式分布的。通常只有腹侧是向性敏感的;也就是说,敏感性是单侧分布的。在这种情况下存在向性作用,因为当敏感表面仅受到部分刺激时,会随之发生肌肉的不等收缩,这会导致敏感表面处于一种状态,即所有部分都受到同等刺激。随后会出现均等的肌肉张力,生物体与环境达到平衡。