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

机译:失神经或肉毒中毒大鼠骨骼肌中乙酰胆碱的含量和释放

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摘要

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.
机译:1.通过热解-质谱分析法测定大鼠趾长伸肌(EDL)肌肉中乙酰胆碱(ACh)的含量以及乙酰胆碱的自发和诱发释放。测定是通过局部应用A型肉毒杆菌毒素使瘫痪的肌肉,无毒的肌肉,经神经支配或经神经支配的肌肉进行的。2。在动物之间,未中毒的对照肌肉的ACh含量几乎是均匀的,并且在36至50 pmol的实验序列中变化。 BoTx在中毒2天后未能影响ACh含量,而在8天后导致其含量略有增加。手术去神经支配后24小时内ACh含量降至神经支配肌肉的10%以下,并且在重新神经支配后ACh含量得以恢复。胆碱酯酶抑制后,神经支配和神经支配的ACh含量随时间增加约3。正常神经支配的肌肉中ACh的自发释放在40至100 fmol / min之间。在25mm-KCl存在下,释放速率增加约四倍。在BoTx中,中毒后2 d肌肉中的自发释放减少了多达60%的控制,高钾未能加速释放,而在8 d时仅引起少量增加。失神经的肌肉释放ACh的速率低于对照组的20%,而高钾不能加速ACh的释放。4。结果表明,受神经支配的EDL肌肉中总ACh的90%以上存在于神经及其末端。剩余的乙酰胆碱显然形成并储存在肌肉组织中。 BoTx导致的ACh释放降低幅度大于假定选择性阻滞发射机的定量释放所导致的幅度。这表明,BoTx对非定量ACh释放也具有抑制作用。

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