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降钙素基因相关肽对大鼠输精管交感神经末梢神经效应机制的影响。

Effect of calcitonin gene-related peptide on the neuroeffector mechanism of sympathetic nerve terminals in rat vas deferens.

作者信息

Ohhashi T, Jacobowitz D M

出版信息

Peptides. 1985 Sep-Oct;6(5):987-91. doi: 10.1016/0196-9781(85)90332-8.

Abstract

In order to evaluate the mode of action of calcitonin gene-related peptide (CGRP) on the neuroeffector mechanism of peripheral sympathetic nerve fibers, the effects of CGRP were tested on the electrical stimulated and the non-stimulated preparations of the isolated rat vas deferens. The contractile responses, which were mediated predominantly by activation of postganglionic noradrenergic nerve fibers, were dose-dependently inhibited by CGRP in concentrations ranging from 0.1 to 10 nM. The inhibitory response produced by CGRP in high concentrations (greater than 2 nM) usually returned to the control level at 20-30 min and were rarely tachyphylactic. The inhibitory action of CGRP was not modified by pretreatment with 10(-7) M propranolol or 10(-7) M atropine. Contractions produced by exogenous norepinephrine (NE) and 5-hydroxytryptamine (5-HT) in unstimulated preparations were not affected by pretreatment with CGRP in a low concentration (less than 2 nM). On the other hand, the contractions were slightly reduced 1 min after pretreatment with CGRP in high concentrations (greater than 5 nM), which recovered in 15 min after constant flow washout. High concentrations of CGRP also caused a concentration-dependent relaxation on the precontracted preparations produced by high potassium (60 mM K+) solution. These results suggest that CGRP in high concentrations (greater than 5 nM) may have a non-specific inhibitory action on the postsynaptic plasma membrane of the smooth muscle cell and a postulated CGRP receptor exists presynaptically in the rat vas deferens and that CGRP may inhibit the release of NE during adrenergic nerve stimulation.

摘要

为了评估降钙素基因相关肽(CGRP)对周围交感神经纤维神经效应机制的作用方式,在分离的大鼠输精管的电刺激和非刺激制剂上测试了CGRP的作用。主要由节后去甲肾上腺素能神经纤维激活介导的收缩反应,在浓度范围为0.1至10 nM的CGRP作用下呈剂量依赖性抑制。高浓度(大于2 nM)的CGRP产生的抑制反应通常在20 - 30分钟时恢复到对照水平,且很少出现快速耐受性。CGRP的抑制作用不会因用10⁻⁷ M普萘洛尔或10⁻⁷ M阿托品预处理而改变。在未刺激的制剂中,外源性去甲肾上腺素(NE)和5 - 羟色胺(5 - HT)产生的收缩不受低浓度(小于2 nM)CGRP预处理的影响。另一方面,高浓度(大于5 nM)CGRP预处理1分钟后,收缩略有降低,在持续冲洗15分钟后恢复。高浓度的CGRP也会对由高钾(60 mM K⁺)溶液产生的预收缩制剂产生浓度依赖性舒张作用。这些结果表明,高浓度(大于5 nM)的CGRP可能对平滑肌细胞的突触后质膜具有非特异性抑制作用,并且在大鼠输精管中假定的CGRP受体存在于突触前,并且CGRP可能在肾上腺素能神经刺激期间抑制NE的释放。

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