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维生素A缺乏大鼠中慢适应性I型皮肤机械感受器的反应性和超微结构

Responsiveness and ultrastructure of slowly adapting type I cutaneous mechanoreceptors in vitamin A deficient rats.

作者信息

Baumann K I, Cheng-Chew S B, Hamann W, Leung M S

出版信息

J Physiol. 1986 Feb;371:339-49. doi: 10.1113/jphysiol.1986.sp015979.

Abstract

Single-unit recordings were made from afferent nerve fibres supplying slowly adapting type I (s.a. I) cutaneous mechanoreceptors in anaesthetized vitamin A deficient and control rats. Trains of thirty repetitive mechanical stimuli with 0.1 s rise time, 1.9 s plateau phase, and 0.7 s interstimulus interval were applied. A feed-back mechanism maintained the force of stimulation at 20 mN during the plateau phases and the contact force between stimuli at 0.5 mN. All displacement values in the group of vitamin A deficient rats were significantly larger than the corresponding control values. Residual indentations were increased by 70-100% while maximal indentations were only about 40% higher. These results indicate a non-linear increase in compliance of the skin and underlying tissues. S.a. I receptors were found to be significantly less responsive in vitamin A deficient animals. Mean numbers of impulses were about 25% lower in the vitamin A deficient group than in controls throughout the entire train of thirty stimuli. In vitamin A deficient rats, Merkel cells and adjoining nerve terminals showed signs of degeneration of a variety of cell organelles, particularly the mitochondria. Degenerative changes induced by vitamin A deficiency especially in the Merkel cells appeared to be a major cause of the reduction of responsiveness in s.a. I receptors.

摘要

在麻醉状态下的维生素A缺乏大鼠和对照大鼠中,对供应缓慢适应性I型(s.a. I)皮肤机械感受器的传入神经纤维进行单单位记录。施加了一系列30次重复的机械刺激,上升时间为0.1秒,平台期为1.9秒,刺激间隔为0.7秒。反馈机制在平台期将刺激力维持在20毫牛顿,并使刺激之间的接触力保持在0.5毫牛顿。维生素A缺乏大鼠组的所有位移值均显著大于相应的对照值。残余压痕增加了70 - 100%,而最大压痕仅高出约40%。这些结果表明皮肤和下层组织的顺应性呈非线性增加。发现s.a. I感受器在维生素A缺乏的动物中反应明显减弱。在整个30次刺激序列中,维生素A缺乏组的平均冲动数比对照组低约25%。在维生素A缺乏的大鼠中,默克尔细胞和相邻的神经末梢显示出各种细胞器,特别是线粒体的退化迹象。维生素A缺乏引起的退化性变化,尤其是在默克尔细胞中,似乎是s.a. I感受器反应性降低的主要原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1279/1192728/a55556b74f8b/jphysiol00559-0361-a.jpg

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