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甘油处理对蟾蜍缝匠肌纤维膜容量和兴奋-收缩偶联的不同影响。

Differential effects of glycerol treatment on membrane capacity and excitation-contraction coupling in toad sartorius fibres.

作者信息

Dulhunty A F, Gage P W

出版信息

J Physiol. 1973 Oct;234(2):373-408. doi: 10.1113/jphysiol.1973.sp010350.

DOI:10.1113/jphysiol.1973.sp010350
PMID:4203309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1350633/
Abstract

Changes in membrane capacity and excitation-contraction coupling caused by glycerol movements have been investigated in toad sartorius fibres using a standard glycerol-Ringer solution containing 400 mM glycerol.1. The rates of glycerol movement, in and out of fibres, were determined by measuring diameter changes in single fibres. Glycerol equilibrated across the surface membrane within 20-25 min after changes in extracellular glycerol concentration.2. The reduction in membrane capacity, which occurs when glycerol-loaded fibres are returned to Ringer solution, was slower than, and not dependent on, changes in fibre volume.3. To obtain the maximum reduction in membrane capacity, it was necessary to expose fibres to glycerol-Ringer for 50-60 min and then to return them to Ringer for at least 60 min. If preparations were not kept in Ringer for the full 50-60 min, the reduction in membrane capacity could be partially or completely reversed by returning the fibres to glycerol-Ringer.4. When fibres were exposed to glycerol-Ringer there was an initial transient contracture: twitches and K contractures were rapidly inhibited, and then slowly recovered over the next 40-50 min. In some preparations, eventual potentiation of twitches was seen.5. When returned to Ringer solution after 60 min in glycerol-Ringer, preparations lost twitches and K contractures within 5-10 min. The time course of this effect was very similar to the time course of the recovery of the normal volume after the initial swelling.6. The briefer the exposure to the glycerol-Ringer, the slower the loss of twitches and K contractures on return to Ringer. In contrast to the loss of membrane capacity, the lesion of excitation-contraction coupling was essentially irreversible. Exposure times as brief as 5 min were eventually effective in producing paralysed fibres which, however, still responded to caffeine.7. The differences in the glycerol load-times required to produce decoupling of excitation and contraction, and disconnexion of the transverse tubules, show that the two effects are separable and that the first does not depend on the second.8. It is proposed that the two lesions obtained in glycerol-treated fibres may be related to distension of the transverse tubular system. It is shown in an Appendix that the outward movement of glycerol from sarcoplasm to transverse tubules would be expected to produce some early swelling of the tubules and this is related to the loss of contraction. Furthermore, much greater swelling would occur if a slow-loading compartment (presumed to be the sarcoplasmic reticulum) dumped glycerol into the transverse tubules: it is thought that this is related to the disconnexion of the transverse tubules.

摘要

利用含有400 mM甘油的标准甘油 - 林格液,对蟾蜍缝匠肌纤维中由甘油移动引起的膜电容变化和兴奋 - 收缩偶联进行了研究。1. 通过测量单根纤维的直径变化来确定甘油进出纤维的速率。细胞外甘油浓度改变后,甘油在20 - 25分钟内穿过表面膜达到平衡。2. 当用甘油处理过的纤维再回到林格液中时,膜电容的降低比纤维体积的变化慢,且与纤维体积变化无关。3. 为了使膜电容达到最大程度的降低,有必要将纤维暴露于甘油 - 林格液中50 - 60分钟,然后再将它们放回林格液中至少60分钟。如果制剂在林格液中放置的时间不足完整的50 - 60分钟,将纤维再放回甘油 - 林格液中,膜电容的降低可能会部分或完全逆转。4. 当纤维暴露于甘油 - 林格液中时,最初会出现短暂的挛缩:抽搐和K挛缩迅速受到抑制,然后在接下来的40 - 50分钟内缓慢恢复。在一些制剂中,最终会出现抽搐增强的现象。5. 在甘油 - 林格液中放置60分钟后再回到林格液中,制剂在5 - 10分钟内失去抽搐和K挛缩。这种效应的时间进程与最初肿胀后正常体积恢复的时间进程非常相似。6. 暴露于甘油 - 林格液的时间越短,回到林格液后抽搐和K挛缩丧失的速度就越慢。与膜电容的丧失不同,兴奋 - 收缩偶联的损伤基本上是不可逆的。短至5分钟的暴露时间最终也能有效地使纤维麻痹,不过这些纤维仍对咖啡因有反应。7. 产生兴奋与收缩解偶联以及横管断开所需的甘油加载时间差异表明,这两种效应是可分离的,且第一种效应不依赖于第二种效应。8. 有人提出,在甘油处理过的纤维中出现的这两种损伤可能与横管系统的扩张有关。附录中表明,甘油从肌浆向外移动到横管预计会使横管出现一些早期肿胀,这与收缩丧失有关。此外,如果一个缓慢加载的隔室(推测为肌浆网)将甘油倾倒入横管中,将会发生更大程度的肿胀:据认为这与横管的断开有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2be/1350633/d62b2e2ae668/jphysiol00950-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2be/1350633/d62b2e2ae668/jphysiol00950-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2be/1350633/d62b2e2ae668/jphysiol00950-0172-a.jpg

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