Yun S, Shoumura K, Ichinohe N, Hirama H, Amayasu H
Department of Anatomy, Hirosaki University School of Medicine, Japan.
J Hirnforsch. 1995;36(1):29-50.
Pupillary responses were studied by electrical stimulation of the posterior commissure (PC) and the nuclei of origin and termination of PC fibers in the cat. Prior to stimulation experiments, cervical sympathectomy was carried out to study the pupillary responses not mediated by the ocular sympathetic nerve. Pupillary responses were recorded by using an infrared pupillo-analyzing system. The stimulus consisted of a 5 s train of cathodal square wave (0.5 ms duration, 50 Hz) pulses. Stimulation of the PC evoked a pupillary response complex (PRC), which began with a rapid pupillary constriction after the latency of 210-317 ms. The threshold of constriction was 10 or 20 microA. Constriction reached its peak shortly after the onset of the stimulus, then the pupil gradually re-dilated (pupillary escape, PE) even though the stimulus was still lasting. The pupil gradually returned, after stimulus termination, to the size before stimulation in the cases with the pupil area before stimulation larger than 20 mm2. On the other hand, in the cases with smaller pupil area before stimulation (< 20 mm2), rapid constriction and PE were followed, after stimulus termination, by a large dilation (after-dilation, AD). The thresholds of PE and AD were 20 or 40 microA. Pupillary constriction was evoked with a large range of stimulus frequency (1-100 Hz). To evoke PE and AD, stimulus frequencies of 10 and 50 Hz were required respectively, and lower frequencies were ineffective. The peak latency of AD increased in proportion to the increase in stimulus frequency and intensity. Following horseradish peroxidase (dissolved in 5% alkyl-phenol ethylene oxide) injection into the pretectal region where fibers from the PC fan out, retrogradely labeled neurons occurred in many subthalamic, pretectal and midbrain nuclei on the other side. They were classified into three groups in terms of the pupillary response evoked by electrical stimulation; the pupillo-constrictory nuclei (PCNs) of which stimulation evoked constriction with the threshold of 20 microA, the pupillo-dilatory nuclei (PDNs) of which stimulation evoked dilation with the threshold of 20 or 10 microA, and other nuclei with higher thresholds of constriction or dilation. The PDNs were further, classified into two groups (Type 1 and Type 2 PDNs) according to the relationship between stimulus intensity and the peak latency of dilation.(ABSTRACT TRUNCATED AT 400 WORDS)
通过电刺激猫的后连合(PC)以及PC纤维的起始核和终末核来研究瞳孔反应。在刺激实验之前,进行颈交感神经切除术以研究不由眼交感神经介导的瞳孔反应。使用红外瞳孔分析系统记录瞳孔反应。刺激由一串持续5秒的阴极方波(持续时间0.5毫秒,频率50赫兹)脉冲组成。刺激PC会诱发瞳孔反应复合体(PRC),其在210 - 317毫秒的潜伏期后开始出现快速瞳孔收缩。收缩阈值为10或20微安。收缩在刺激开始后不久达到峰值,然后即使刺激仍在持续,瞳孔也会逐渐重新扩张(瞳孔逃逸,PE)。在刺激前瞳孔面积大于20平方毫米的情况下,刺激终止后,瞳孔会逐渐恢复到刺激前的大小。另一方面,在刺激前瞳孔面积较小(<20平方毫米)的情况下,快速收缩和PE之后,刺激终止后会出现大的扩张(后扩张,AD)。PE和AD的阈值分别为20或40微安。在很宽的刺激频率范围(1 - 100赫兹)内都能诱发瞳孔收缩。要诱发PE和AD,分别需要10赫兹和50赫兹的刺激频率,较低频率无效。AD的峰值潜伏期与刺激频率和强度的增加成比例增加。将辣根过氧化物酶(溶解于5%烷基酚环氧乙烷)注入PC纤维发散的顶盖前区后,在另一侧的许多丘脑底核、顶盖前核和中脑核中出现了逆行标记的神经元。根据电刺激诱发的瞳孔反应,将它们分为三组;刺激阈值为20微安时诱发收缩的瞳孔收缩核(PCNs),刺激阈值为20或10微安时诱发扩张的瞳孔扩张核(PDNs),以及收缩或扩张阈值较高的其他核。根据刺激强度与扩张峰值潜伏期之间的关系,PDNs进一步分为两组(1型和2型PDNs)。