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降钙素基因相关肽可兴奋肠肌间神经元。

Calcitonin gene-related peptide excites myenteric neurons.

作者信息

Palmer J M, Schemann M, Tamura K, Wood J D

出版信息

Eur J Pharmacol. 1986 Dec 16;132(2-3):163-70. doi: 10.1016/0014-2999(86)90601-1.

Abstract

Intracellular methods were used to record electrical behavior of myenteric neurons in guinea-pig ileum in vitro. Calcitonin gene-related peptide (CGRP; 1 nM to 1 microM) and calcitonin (1-100 microM) were applied by addition to the superfusion solution of longitudinal muscle-myenteric plexus preparations. Both peptides were applied also by pressure ejection from fine-tipped micropipettes. CGRP, applied by either method, evoked a long-lasting depolarization of the cell membranes that was dose-dependent (ED50 = 50 nM) and was associated with an increase in the input resistance, suppression of post-spike hyperpolarizing potentials and enhanced excitability in all neurons that were tested. The enhanced excitability was reflected by a significant increase in the number of action potentials evoked by intracellular injection of constant current depolarizing pulses. Enhanced excitability also was apparent as a train of spikes that appeared at the crests of the CGRP-induced depolarization. The excitatory action of CGRP simulated slow synaptic excitation. Application of calcitonin did not evoke any changes in electrical behavior of myenteric neurons. The results are consistent with a neurotransmitter or neuromodulator role for CGRP in the enteric nervous system and suggest that it may participate in local neurohumoral regulation of gastrointestinal effector systems.

摘要

采用细胞内记录方法,在体外记录豚鼠回肠肌间神经丛神经元的电活动。通过向纵行肌-肌间神经丛标本的灌流液中添加降钙素基因相关肽(CGRP;1 nM至1 μM)和降钙素(1 - 100 μM)来进行实验。这两种肽也通过细尖微吸管的压力喷射来施加。通过这两种方法施加的CGRP均能引起细胞膜的持久去极化,该去极化呈剂量依赖性(半数有效剂量 = 50 nM),并伴有输入电阻增加、峰后超极化电位受抑制以及所有受试神经元兴奋性增强。兴奋性增强表现为通过细胞内注入恒定电流去极化脉冲诱发的动作电位数量显著增加。兴奋性增强在CGRP诱发的去极化波峰处出现一连串尖峰时也很明显。CGRP的兴奋作用模拟了缓慢的突触兴奋。降钙素的施加未引起肌间神经丛神经元电活动的任何变化。这些结果与CGRP在肠神经系统中作为神经递质或神经调节剂的作用一致,并表明它可能参与胃肠道效应系统的局部神经体液调节。

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