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大鼠骨骼肌神经末梢降钙素基因相关肽的释放。

Release of calcitonin gene-related peptide from nerve terminals in rat skeletal muscle.

作者信息

Sakaguchi M, Inaishi Y, Kashihara Y, Kuno M

机构信息

National Institute for Physiological Sciences, Okazaki, Japan.

出版信息

J Physiol. 1991 Mar;434:257-70. doi: 10.1113/jphysiol.1991.sp018468.

Abstract
  1. The amount of calcitonin gene-related peptide (CGRP) released from the isolated rat soleus muscle was measured by enzyme immunoassay. 2. When the soleus muscle was exposed to a solution containing high K+ (20-100 mM) in the presence of tetrodotoxin, the amount of CGRP released into the bathing medium increased with an increase in the K+ concentration. 3. The exposure to 100 mM-K+ did not increase CGRP release from chronically denervated soleus muscles or from pieces of the soleus nerve separated from the muscle. 4. The amount of CGRP released from the isolated muscle by 100 mM-K+ depended on the external Ca2+ concentration. The slope of the relation between the amount of CGRP release and the Ca2+ concentration was less than one on double logarithmic co-ordinates. 5. Following chronic section of the lumbar ventral roots, the mean amount of CGRP released from the soleus muscle by 100 mM-K+ was reduced by 28%, compared with that observed in normal muscle. 6. Antidromic stimulation of the lumbar dorsal roots at an intensity three times the threshold for most excitable sensory fibres failed to induce CGRP release from the soleus muscle, whereas stimulation at intensities 50-100 times the threshold increased significantly the amount of CGRP release from the muscle. 7. Stimulation of the muscle nerve at an intensity sufficient to activate the alpha-motor fibres did not release CGRP from the soleus muscle or from the diaphragm. 8. It is concluded that the major source of CGRP released from skeletal muscle is A delta- and/or C sensory terminals and that the Ca2+ dependence of CGRP release is less steep than that reported for acetylcholine release at neuromuscular junctions.
摘要
  1. 通过酶免疫测定法测量从分离的大鼠比目鱼肌释放的降钙素基因相关肽(CGRP)的量。2. 当比目鱼肌在存在河豚毒素的情况下暴露于含有高钾(20 - 100 mM)的溶液中时,释放到浴液中的CGRP量随钾离子浓度的增加而增加。3. 暴露于100 mM - K + 不会增加慢性去神经支配的比目鱼肌或从肌肉分离的比目鱼神经片段中CGRP的释放。4. 100 mM - K + 从分离的肌肉中释放的CGRP量取决于细胞外钙离子浓度。在双对数坐标上,CGRP释放量与钙离子浓度之间关系的斜率小于1。5. 腰腹侧神经根慢性切断后,与正常肌肉相比,100 mM - K + 从比目鱼肌释放的CGRP平均量减少了28%。6. 以大多数易兴奋感觉纤维阈值的三倍强度对腰背根进行逆向刺激未能诱导比目鱼肌释放CGRP,而以阈值的50 - 100倍强度刺激则显著增加了肌肉中CGRP的释放量。7. 以足以激活α运动纤维的强度刺激肌肉神经不会从比目鱼肌或膈肌中释放CGRP。8. 得出的结论是,骨骼肌释放的CGRP的主要来源是Aδ和/或C感觉末梢,并且CGRP释放对钙离子的依赖性不如神经肌肉接头处乙酰胆碱释放所报道的那样陡峭。

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