首页> 外文期刊>Neurogastroenterology and motility >Effect of calcitonin gene-related peptide (CGRP) on motility and on the release of substance P, neurokinin A, somatostatin and gastrin in the isolated perfused porcine antrum.
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Effect of calcitonin gene-related peptide (CGRP) on motility and on the release of substance P, neurokinin A, somatostatin and gastrin in the isolated perfused porcine antrum.

机译:降钙素基因相关肽(CGRP)对分离的灌注猪胃腔中的运动以及对P物质,神经激肽A,生长抑素和胃泌素释放的影响。

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摘要

We studied the effect of porcine CGRP (pCGRP) in concentrations from 10(-10) to 10(-8) mol L(-1) on the motility and on the release of substance P, neurokinin A, somatostatin and gastrin in the antrum using the isolated perfused porcine antrum as experimental model. In addition, we studied the localization of CGRP by immunohistochemistry in the porcine antrum. CGRP-immunoreactive nerve fibres were found mainly in the submucous layer and in the external muscle coat, where they were seen in all layers, and in the ganglia of the myenteric nervous plexus. The frequency of contraction was significantly and dose-dependently increased from a basal level of 11.8 +/- 0.5 contractions per 5 min to 24.4 +/- 3.6 contractions per 5 min at pCGRP 10(-8) mol L(-1). At this dose, the release of substance P and neurokinin A was significantly increased to 470 +/- 149% and 217 +/- 26%, respectively, compared to basal release. The effect of pCGRP was unaffected by the addition of the nonpeptide antagonists for the NK-1 (CP-99994) and NK-2 receptors (SR48968), both at 10(-6) mol L(-1), whereas atropine (10(-6) mol L(-1)) completely abolished the motor effect of pCGRP. The release of somatostatin was significantly increased by 154 +/- 15% in response to CGRP at 10(-8) mol L(-1). The release of gastrin was unaffected by pCGRP. In conclusion, pCGRP increases contractile activity in the porcine antrum, an effect that involves cholinergic mechanisms but is independent of the release of substance P and neurokinin A. in addition, pCGRP increases the release of somatostatin but has no effect on gastrin release in the isolated perfused porcine antrum.
机译:我们研究了猪CGRP(pCGRP)浓度从10(-10)到10(-8)mol L(-1)对运动的影响以及对胃中P物质,神经激肽A,生长抑素和胃泌素释放的影响使用分离的灌注猪窦作为实验模型。另外,我们通过免疫组织化学研究了猪胃中CGRP的定位。 CGRP免疫反应性神经纤维主要存在于粘膜下层和外肌被膜中,在所有层中均可见,并存在于肌层神经丛的神经节中。在pCGRP 10(-8)mol L(-1)下,收缩的频率显着且剂量依赖性地从每5分钟11.8 +/- 0.5收缩的基础水平增加到每5分钟24.4 +/- 3.6收缩。在该剂量下,与基础释放相比,物质P和神经激肽A的释放分别显着增加至470 +/- 149%和217 +/- 26%。加入10(-6)mol L(-1)的NK-1(CP-99994)和NK-2受体(SR48968)的非肽拮抗剂不会影响pCGRP的作用,而阿托品(10 (-6)mol L(-1))完全废除了pCGRP的运动作用。生长激素抑制素的释放在10(-8)mol L(-1)下响应CGRP显着增加154 +/- 15%。胃泌素的释放不受pCGRP的影响。总之,pCGRP增加了猪胃中的收缩活性,这种作用涉及胆碱能机制,但与P物质和神经激肽A的释放无关。此外,pCGRP增加了生长抑素的释放,但对分离物中胃泌素的释放没有影响。灌注猪胃腔。

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