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破伤风毒素对小鼠慢、快骨骼肌神经肌肉传递及运动终板形态的影响。

The effects of tetanus toxin on neuromuscular transmission and on the morphology of motor end-plates in slow and fast skeletal muscle of the mouse.

作者信息

Duchen L W, Tonge D A

出版信息

J Physiol. 1973 Jan;228(1):157-72. doi: 10.1113/jphysiol.1973.sp010078.

Abstract
  1. A sublethal dose of tetanus toxin was injected into the muscles of one hind leg of the mouse and caused local tetanus which persisted for 4 weeks.2. Neuromuscular transmission was studied in vitro in nerve-muscle preparations of soleus, a slow muscle, and extensor digitorum longus (EDL), a fast muscle, from 1 day to 6 months after the injection of toxin.3. Soleus failed to respond to nerve stimulation, became supersensitive to acetylcholine and showed spontaneous fibrillations for several weeks before returning to normal. EDL did not show these changes. A higher dose of tetanus toxin, lethal within 24 hr, caused paralysis of EDL as well as soleus.4. In muscle fibres in which neuromuscular transmission was blocked spontaneous miniature end-plate potentials (m.e.p.p.s) were recorded. The frequency of m.e.p.p.s was increased by repetitive nerve stimulation but not by raising the external potassium concentration.5. The amplitude of spontaneous m.e.p.p.s showed a skew distribution because of a disproportionate number of potentials of less than 0.2 mV.6. Raising the external calcium concentration did not restore neuromuscular transmission.7. Histological examination of soleus showed atrophy of muscle fibres with normal preterminal axons. There was sprouting from motor nerve terminals and subsequently new motor end-plates were formed. These changes were not found in EDL.8. The results indicate that, in the mouse, tetanus toxin causes a presynaptic block of neuromuscular transmission and ;functional denervation' of muscle. Slow muscle is more sensitive to the effects of the toxin than fast.
摘要
  1. 将亚致死剂量的破伤风毒素注射到小鼠一条后腿的肌肉中,引发了持续4周的局部破伤风。

  2. 在注射毒素后1天至6个月期间,对来自比目鱼肌(一种慢肌)和趾长伸肌(EDL,一种快肌)的神经 - 肌肉标本进行了体外神经肌肉传递研究。

  3. 比目鱼肌对神经刺激无反应,对乙酰胆碱变得超敏,并在恢复正常前数周出现自发纤维颤动。EDL未出现这些变化。更高剂量的破伤风毒素在24小时内致死,导致EDL和比目鱼肌均麻痹。

  4. 在神经肌肉传递被阻断的肌纤维中记录到了自发的微小终板电位(m.e.p.p.s)。m.e.p.p.s的频率通过重复神经刺激增加,但不通过提高细胞外钾浓度增加。

  5. 由于小于0.2 mV的电位数量不成比例,自发m.e.p.p.s的幅度呈现偏态分布。

  6. 提高细胞外钙浓度未能恢复神经肌肉传递。

  7. 比目鱼肌的组织学检查显示肌纤维萎缩,终末前轴突正常。运动神经末梢有芽生,随后形成了新的运动终板。这些变化在EDL中未发现。

  8. 结果表明,在小鼠中,破伤风毒素导致神经肌肉传递的突触前阻滞和肌肉的“功能性去神经支配”。慢肌比快肌对毒素的作用更敏感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b66a/1331232/d74b91356fd5/jphysiol00973-0174-a.jpg

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