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在离体豚鼠小肠中由肠抑制反射介导的适应性调节。

Accommodation mediated by enteric inhibitory reflexes in the isolated guinea-pig small intestine.

作者信息

Waterman S A, Costa M, Tonini M

机构信息

Department of Human Physiology, School of Medicine, Flinders University of South Australia, Adelaide.

出版信息

J Physiol. 1994 Feb 1;474(3):539-46. doi: 10.1113/jphysiol.1994.sp020043.

Abstract
  1. The aim of the present study was to investigate whether the guinea-pig small intestine shows accommodation to infused fluid, similarly to other regions of the gastrointestinal tract. Tetrodotoxin, papaverine and transmitter antagonists were used to establish the existence of reflex pathways and the nature of the neurotransmitters involved. 2. Compliance, measured as the change in volume of infused fluid divided by the intraluminal pressure change, was reduced by tetrodotoxin (0.6 microM), indicating that there is an overall neurally mediated relaxation of the circular muscle in response to low rates of distension. Papaverine (10 microM) did not have any significant effect on compliance at the low rates of distension, suggesting that the circular muscle is fully relaxed. 3. At each rate of distension, 400 microM N omega-nitro-L-arginine methyl ester (L-NAME, a nitric oxide synthase inhibitor) significantly decreased the compliance of the intestinal wall, indicating that the circular muscle was relaxed by a nitric oxide-mediated mechanism. Apamin (0.5 microM), which blocks a component of inhibitory transmission, did not have a significant effect. 4. In control preparations, the intestinal wall was less compliant when distended by fluid at a fast rate, compared with the lower rates of distension. This was not due to changes in passive components of the intestinal wall or a myogenic response to rapid stretch. 5. When the intestine was distended rapidly, 1 microM hyoscine and 100 microM hexamethonium increased intestinal compliance. However, they had no detectable effect on compliance with low rates of distension.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 本研究的目的是调查豚鼠小肠是否像胃肠道的其他区域一样,对输注液体表现出适应性。使用河豚毒素、罂粟碱和递质拮抗剂来确定反射途径的存在以及所涉及神经递质的性质。2. 顺应性通过输注液体体积变化除以腔内压力变化来衡量,河豚毒素(0.6微摩尔)可降低顺应性,这表明在低扩张速率下,环形肌存在整体神经介导的舒张。罂粟碱(10微摩尔)在低扩张速率下对顺应性没有显著影响,这表明环形肌已完全舒张。3. 在每个扩张速率下,400微摩尔N-ω-硝基-L-精氨酸甲酯(L-NAME,一种一氧化氮合酶抑制剂)显著降低肠壁顺应性,这表明环形肌通过一氧化氮介导的机制舒张。蜂毒明肽(0.5微摩尔)可阻断抑制性传递的一个成分,但其没有显著影响。4. 在对照制剂中,与较低扩张速率相比,快速输注液体时肠壁顺应性较低。这不是由于肠壁被动成分的变化或对快速拉伸的肌源性反应。5. 当小肠快速扩张时,1微摩尔东莨菪碱和100微摩尔六甲铵可增加肠顺应性。然而,它们对低扩张速率下的顺应性没有可检测到的影响。(摘要截短于250字)

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