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蝾螈横纹肌再支配过程中突触的形成与消退

The formation and regression of synapses during the re-innervation of axolotl striated muscles.

作者信息

Bennett M R, Raftos J

出版信息

J Physiol. 1977 Feb;265(2):261-95. doi: 10.1113/jphysiol.1977.sp011716.

DOI:10.1113/jphysiol.1977.sp011716
PMID:191597
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1307820/
Abstract
  1. A study has been made of the formation and regression of synapses formed by spinal nerves 16 and 17 in axolotl hind-limb flexor muscles following the severing of nerve 16, using histological, ultrastructural and electrophysiological techniques. 2. Axolotl hind-limb flexor myofibres possessed 'en plaque' end-plates from either spinal nerve 16 or 17 or both at intervals of about 1000 micronm along their length; the myofibre's length constant was about 700 micronm allowing electrophysiological observations of at least two of these synapses during a single impalement; transmitter release at these synapses could be described by binomial statistics and in a given set of ionic conditions the binomial statistic parameter n was directly proportional to the size of the nerve terminals whilst the binomial statistic parameter p was invariant to changes in nerve terminal size. 3. The distribution of synapses formed by spinal nerves 16 and 17 in different sectors of the axolotl hind-limb flexor muscles was determined from a study of evoked end-plate potentials; the middle and proximal sectors of the flexor muscles contained myofibres which received an innervation from nerve 16 only, whereas the sectors surrounding these contained myofibres innervated either by nerve 16 or nerve 17 or by both nerves. 4. Six days following the severing of spinal nerve 16, evoked transmitter release from the synapses formed by this nerve had failed; transmission was subsequently recorded at a few synapses formed by nerve 17 in the middle and proximal sectors of the flexor muscles which are not normally innervated by this nerve and these synapses had a low n; during the succeeding four weeks the value of n at the synapses increased to a size about 70% that of the terminals normally formed by nerve 16 at these sites. 5. Four weeks after severing nerve 16, myofibres which possessed synapses formed by nerve 17 also possessed synapses from re-innervating nerve 16 and these were sometimes formed at the same synaptic sites as those occupied by nerve 17. 6. In the subsequent sixteen weeks, the n value of synapses formed by nerve 17 declined whilst the n values of synapses formed by re-innervating nerve 16 on the same myofibres matured to their control size. 7. It is suggested that on severing nerve 16 collateral sprouting of nearby intact nerve 17 occurs and these collateral sprouts innervate the denervated synaptic sites, although the sprouts arenot as well matched to the denervated synaptic sites as are the original nerve terminals; thus if nerve 16 returns it preferentially forms synapses at its original synaptic sites, and the collateral synapses formed by nerve 17 regress.
摘要
  1. 运用组织学、超微结构和电生理学技术,对蝾螈后肢屈肌中由第16和17对脊神经形成的突触在切断第16对神经后的形成和消退进行了研究。2. 蝾螈后肢屈肌肌纤维沿其长度每隔约1000微米具有来自第16或17对脊神经或两者的“板状”终板;肌纤维的长度常数约为700微米,这使得在单次刺入时能够对至少两个这些突触进行电生理学观察;这些突触处的递质释放可用二项式统计来描述,在给定的一组离子条件下,二项式统计参数n与神经末梢的大小成正比,而二项式统计参数p对神经末梢大小的变化不变。3. 通过对诱发终板电位的研究,确定了第16和17对脊神经在蝾螈后肢屈肌不同区域形成的突触分布;屈肌的中部和近端区域包含仅接受第16对神经支配的肌纤维,而围绕这些区域的区域包含由第16对神经或第17对神经或两者支配的肌纤维。4. 切断第16对脊神经六天后,由该神经形成的突触的诱发递质释放失败;随后在屈肌中部和近端区域由第17对神经形成的一些突触处记录到传递,这些区域通常不由该神经支配,并且这些突触的n值较低;在随后的四周内,这些突触处的n值增加到正常由第16对神经在这些部位形成的末梢大小的约70%。5. 切断第16对神经四周后,具有由第17对神经形成的突触的肌纤维也具有来自重新支配的第16对神经的突触,并且这些突触有时在与第17对神经占据的相同突触部位形成。6. 在随后的十六周内,由第17对神经形成的突触的n值下降,而由重新支配的第16对神经在相同肌纤维上形成的突触的n值成熟到其对照大小。7. 有人提出,切断第16对神经后,附近完整的第17对神经会发生侧支芽生,这些侧支芽支配去神经支配的突触部位,尽管这些芽与去神经支配的突触部位的匹配程度不如原始神经末梢;因此,如果第16对神经恢复,它会优先在其原始突触部位形成突触,而由第17对神经形成的侧支突触会消退。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46aa/1307820/714fd96bc6bc/jphysiol00821-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46aa/1307820/66e47fa59b2b/jphysiol00821-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46aa/1307820/714fd96bc6bc/jphysiol00821-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46aa/1307820/66e47fa59b2b/jphysiol00821-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46aa/1307820/714fd96bc6bc/jphysiol00821-0036-a.jpg

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