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甲硫氨酸脑啡肽对豚鼠小肠环行肌非肾上腺素能非胆碱能反射运动反应的控制

Control of non-adrenergic non-cholinergic reflex motor responses in circular muscle of guinea-pig small intestine by Met-enkephalin.

作者信息

Ivancheva Chr, Radomirov R

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, Acad. G. Bonchev str., bl.23, 1113 Sofia, Bulgaria.

出版信息

Auton Autacoid Pharmacol. 2002 Aug;22(4):199-207. doi: 10.1046/j.1474-8673.2002.00260.x.

Abstract

1 A triple organ bath method allowing the synchronous recording of the motor activity of the circular muscle layer belonging to the oral and anal segments of guinea-pig small intestine adjacent to an electrically stimulated middle segment was developed to study the ascending and descending reflex motor responses. 2 Electrical field stimulation (0.8 ms, 40 V, 5 Hz, 10 s) applied to the middle part of the segments elicited tetrodotoxin (1 microm)-sensitive ascending and descending contractile responses of the nonstimulated parts, oral and anal, respectively. The ascending contraction was more pronounced as compared with the descending contraction. 3 In the presence of phentolamine (5 microm), propranolol (5 microm) and atropine (3 microm) a significant decrease in the amplitude of the ascending contraction was seen and a descending relaxation, instead of a contraction was observed. 4 Met-enkephalin applied at a single concentration (0.1 microm) or cumulatively (0.001-1 microm) inhibited both non-adrenergic non-cholinergic (NANC) descending relaxation and ascending contraction with similar efficacy but different potency, IC50 being 5.9 +/- 0.3 and 39.0 +/- 4 nm, respectively. Naloxone (0.5 microm) prevented the effects of Met-enkephalin. 5 L-NNA (0.5 mm), an inhibitor of nitric oxide synthesis, increased the ascending contraction and strongly reduced but not abolished the descending relaxation. l-Arginine (0.5 mm) restored the motor responses to the initial level in l-NNA-pretreated preparations, d-Arginine (0.5 nm) had no effects. 6 Met-enkephalin (0.1 microm) depressed the l-NNA-dependent increase of the ascending contraction and failed to change the l-NNA-resistant part of the descending relaxation. 7 Met-enkephalin did not alter spontaneous NANC mechanical activity. SNP (1 or 10 microm), an exogenous donor of nitric oxide, caused a concentration-dependent relaxation. The effects of SNP persisted in Met-enkephalin (0.1 microm)-pretreated preparations. 8 NANC reflex ascending contraction and descending relaxation were synchronously induced by a local nerve stimulation indicating a functional coactivation of NANC orally projected excitatory and anally directed inhibitory pathways. Acting prejunctionally, Met-enkephalin provided a negative controlling mechanism inhibiting both ascending and descending, mainly nitric oxide mediated, reflex responses. A higher sensitivity of the descending relaxation to Met-enkephalin was observed suggesting an essential role of opioid(s) in reducing the efficacy of descending motor activity.

摘要
  1. 为了研究升支和降支反射运动反应,开发了一种三联器官浴方法,该方法可同步记录豚鼠小肠口腔和肛门段环形肌层的运动活动,该段相邻于电刺激的中间段。2. 施加于肠段中部的电场刺激(0.8毫秒,40伏,5赫兹,10秒)分别引起未刺激部分(口腔和肛门)对河豚毒素(1微摩尔)敏感的升支和降支收缩反应。与降支收缩相比,升支收缩更明显。3. 在酚妥拉明(5微摩尔)、普萘洛尔(5微摩尔)和阿托品(3微摩尔)存在的情况下,升支收缩幅度显著降低,并且观察到降支松弛而非收缩。4. 单次浓度(0.1微摩尔)或累积(0.001 - 1微摩尔)应用的甲硫氨酸脑啡肽以相似的效力但不同的效价抑制非肾上腺素能非胆碱能(NANC)降支松弛和升支收缩,IC50分别为5.9±0.3和39.0±4纳米。纳洛酮(0.5微摩尔)可阻止甲硫氨酸脑啡肽的作用。5. L - NNA(0.5毫摩尔),一种一氧化氮合成抑制剂,增加了升支收缩并强烈降低但未消除降支松弛。L - 精氨酸(0.5毫摩尔)使L - NNA预处理制剂中的运动反应恢复到初始水平,D - 精氨酸(0.5纳米)无作用。6. 甲硫氨酸脑啡肽(0.1微摩尔)抑制了L - NNA依赖性的升支收缩增加,并且未能改变降支松弛中对L - NNA耐药的部分。7. 甲硫氨酸脑啡肽未改变自发的NANC机械活动。SNP(1或10微摩尔),一种外源性一氧化氮供体,引起浓度依赖性松弛。SNP的作用在甲硫氨酸脑啡肽(0.1微摩尔)预处理的制剂中持续存在。8. 局部神经刺激同步诱导NANC反射性升支收缩和降支松弛,表明NANC向口腔投射的兴奋性和向肛门定向的抑制性通路存在功能性共同激活。甲硫氨酸脑啡肽在突触前起作用,提供了一种负性控制机制,抑制升支和降支反射反应,主要是一氧化氮介导的反应。观察到降支松弛对甲硫氨酸脑啡肽的敏感性更高,表明阿片类物质在降低降支运动活动效力中起重要作用。

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