首页> 外文期刊>British Journal of Pharmacology >Altered responsiveness of the guinea-pig isolated ileum to smooth muscle stimulants and to electrical stimulation after in situ ischemia
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Altered responsiveness of the guinea-pig isolated ileum to smooth muscle stimulants and to electrical stimulation after in situ ischemia

机译:原位缺血后豚鼠离体回肠对平滑肌刺激物和电刺激的反应性改变

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1 We evaluated changes in contractility of the guinea-pig isolated ileum, using intact segments and myenteric plexus-longitudinal muscle (MPLM) preparations, after several times (5-160 min) of ischemia in situ. 2 Intestinal ischemia was produced by clamping the superior mesenteric artery. Ischemic and nonischemic segments, obtained from the same guinea-pig, were mounted in organ baths containing Krebs-bicarbonate (K-B) solution, maintained at 37℃ and gassed with 95% O_2/5% CO_2. The preparations were allowed to equilibrate for 60 min under continuous superfusion of warm K-B solution and then electrically stimulated at 40 V (0.3 Hz, 3.0 ms). Thereafter, complete noncumulative concentration-response curves were constructed for acetylcholine (ACh), histamine (HIS), potassium chloride (KCl), and barium chloride (BaCl_2). Mean E_(max) (maximal response) values were calculated for each drug. 3 Our study shows that alterations of chemically and electrically evoked contractions are dependent on ischemic periods. It also demonstrates that contractile responses of ischemic tissues to neurogenic stimulation decreases earlier and to a significantly greater extent than the non-nerve mediated responses of the intestinal smooth muscle. Contractile responses to smooth muscle stimulants were all similarly affected by ischemia. Electron microscopy images indicated necrotic neuronal death. The decrease in reactivity of ischemic tissues to electrical stimulation was ameliorated by dexrazoxane, an antioxidant agent. 4 We consider the guinea-pig isolated ileum as a useful model system to study the processes involved in neuronal ischemia, and we propose that the reduction in maximal responses to electrical stimulation is a useful parameter to study neuroprotection.
机译:1我们在原位缺血几次(5-160分钟)后,使用完整节段和肌丛神经-纵肌(MPLM)制剂评估了豚鼠离体回肠的收缩力变化。 2肠系膜上动脉夹闭产生肠缺血。将来自同一只豚鼠的缺血性和非缺血性节段安装在装有Krebs-碳酸氢盐(K-B)溶液的器官浴中,保持在37℃并用95%O_2 / 5%CO_2充气。在温暖的K-B溶液的连续重叠下使制剂平衡60分钟,然后在40 V(0.3 Hz,3.0 ms)下电刺激。此后,构建了乙酰胆碱(ACh),组胺(HIS),氯化钾(KCl)和氯化钡(BaCl_2)的完整的非累积浓度-响应曲线。计算每种药物的平均E_(max)(最大反应)值。 3我们的研究表明,化学和电诱发的收缩改变取决于缺血期。它也证明了缺血组织对神经源性刺激的收缩反应比肠道平滑肌的非神经介导的反应更早,并且下降的幅度更大。对平滑肌兴奋剂的收缩反应同样受到缺血的影响。电子显微镜图像显示坏死性神经元死亡。右雷佐生是一种抗氧化剂,可改善缺血组织对电刺激的反应性。 4我们认为豚鼠离体回肠是研究神经元缺血涉及的过程的有用模型系统,并且我们建议最大程度地减少对电刺激的反应是研究神经保护的有用参数。

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