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去神经支配或肉毒杆菌中毒的大鼠骨骼肌中乙酰胆碱的含量及释放

Acetylcholine content and release in denervated or botulinum poisoned rat skeletal muscle.

作者信息

Polak R L, Sellin L C, Thesleff S

出版信息

J Physiol. 1981;319:253-9. doi: 10.1113/jphysiol.1981.sp013905.

Abstract
  1. The acetylcholine (ACh) content and spontaneous and evoked release of ACh in rat extensor digitorum longus (EDL) muscles were determined by pyrolysis-mass fragmentography. The determinations were made on muscles paralysed by local application of botulinum toxin (BoTx) type A, on unpoisoned muscles, surgically denervated or reinnervated muscles.2. The ACh content of unpoisoned control muscles was nearly uniform between animals and varied in the experimental series between 36 and 50 pmol. BoTx failed to affect the ACh content after 2 d of poisoning and caused a slight increase in content after 8 d. Surgical denervation reduced the ACh content within 24 h to less than 10% of innervated muscles and upon reinnervation the ACh content was restored. Following cholinesterase inhibition the ACh content of innervated and denervated muscles increased somewhat, about equally with time.3. Spontaneous release of ACh varied in normal innervated muscles between 40 and 100 fmol/min. In the presence of 25 mm-KCl the rate of release increased about fourfold. In BoTx poisoned muscles spontaneous release was reduced by up to 60% of control and high potassium failed to accelerate the release at 2 d after poisoning and caused only a small increase at 8 d. Denervated muscles released ACh at a rate which was less than 20% of control and it was not accelerated by high potassium.4. The results show that more than 90% of total ACh in the innervated EDL muscle is present in the nerve and its terminals. The remaining ACh is apparently formed and stored in the muscle tissue. BoTx caused a larger reduction in ACh release than can be accounted for by assuming a selective blockade of quantal release of transmitter. It suggests that BoTx has an inhibitory effect also on non-quantal ACh release.
摘要
  1. 通过热解-质谱碎片分析法测定大鼠趾长伸肌(EDL)中乙酰胆碱(ACh)的含量以及ACh的自发释放和诱发释放。测定对象包括局部应用A型肉毒杆菌毒素(BoTx)致瘫的肌肉、未中毒的肌肉、手术去神经支配或重新神经支配的肌肉。

  2. 未中毒对照肌肉的ACh含量在动物之间几乎一致,在实验系列中为36至50皮摩尔。中毒2天后BoTx未能影响ACh含量,而中毒8天后含量略有增加。手术去神经支配在24小时内使ACh含量降至受神经支配肌肉的不到10%,重新神经支配后ACh含量得以恢复。胆碱酯酶抑制后,受神经支配和去神经支配肌肉的ACh含量均有所增加,且随时间增加程度大致相同。

  3. 正常受神经支配肌肉中ACh的自发释放量在40至100飞摩尔/分钟之间。在25毫摩尔氯化钾存在时,释放速率增加约四倍。在BoTx中毒的肌肉中,自发释放在中毒2天后减少至对照的60%以下,高钾未能加速释放,而在中毒8天后仅引起小幅增加。去神经支配的肌肉释放ACh的速率不到对照的20%,且高钾不能加速其释放。

  4. 结果表明,受神经支配的EDL肌肉中超过90%的总ACh存在于神经及其终末。其余的ACh显然是在肌肉组织中形成并储存的。BoTx导致ACh释放的减少幅度大于假设递质量子释放的选择性阻断所能解释的程度。这表明BoTx对非量子性ACh释放也有抑制作用。

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