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肠抑制性运动神经元在离体豚鼠小肠蠕动中的作用

The role of enteric inhibitory motoneurons in peristalsis in the isolated guinea-pig small intestine.

作者信息

Waterman S A, Costa 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 Jun 15;477 ( Pt 3)(Pt 3):459-68. doi: 10.1113/jphysiol.1994.sp020207.

Abstract
  1. Peristalsis is a co-ordinated motor behaviour in which an anally propagated contraction of the circular muscle propels intraluminal contents. The role of excitatory motoneurons in peristalsis is well established; however the role of enteric inhibitory motoneurons is unknown. 2. A combination of a nitric oxide synthase inhibitor and apamin, which blocks relaxation of the circular muscle of guinea-pig small intestine mediated by enteric inhibitory motoneurons, was used to investigate the role of inhibitory motoneurons in peristalsis in isolated segments of guinea-pig small intestine. 3. N omega-nitro-L-arginine methyl ester (L-NAME, 400 microM) and N omega-nitro-L-arginine (L-NOArg, 100 microM) significantly reduced the threshold volume required to trigger emptying of the intestine. This effect was reversed by L-arginine (4 mM) and L-arginine alone increased the threshold volume for initiation of peristalsis. Sodium nitroprusside (0.1-10 microM), which generates nitric oxide, also increased the threshold volume. L-NAME, L-NOArg, L-arginine and sodium nitroprusside did not alter the maximal intraluminal pressure generated during emptying. Contraction of the longitudinal muscle during the initial phase of fluid infusion was significantly increased by L-NAME and L-NOArg and reduced by sodium nitroprusside (1 nM to 10 microM). 4. Apamin (0.5 microM) did not significantly alter the threshold volume necessary to initiate peristalsis or contraction of the longitudinal muscle. However, the maximal pressure generated when the intestine was emptying was significantly increased. Furthermore, short segments of circular muscle contracted apparently randomly, before peristaltic emptying was triggered. 5. A combination of L-NAME and apamin completely disrupted peristalsis. Contractions of the circular muscle did not always start at the oral end. Stationary contractions as well as contractions propagating orally and anally were observed. 6. It is concluded that enteric inhibitory motoneurons are crucial for peristalsis to occur. They are important in setting the threshold at which peristaltic emptying is triggered, via nitric oxide. They are essential for the propagation of the circular muscle contraction, via an apamin-sensitive mechanism of transmission. Contraction of the longitudinal muscle during peristalsis is partly inhibited by a nitric oxide-mediated mechanism.
摘要
  1. 蠕动是一种协调的运动行为,其中环形肌的肛门传播性收缩推动管腔内的内容物。兴奋性运动神经元在蠕动中的作用已得到充分证实;然而,肠内抑制性运动神经元的作用尚不清楚。2. 一氧化氮合酶抑制剂和蜂毒明肽(可阻断由肠内抑制性运动神经元介导的豚鼠小肠环形肌松弛)的组合被用于研究抑制性运动神经元在豚鼠小肠离体节段蠕动中的作用。3. Nω-硝基-L-精氨酸甲酯(L-NAME,400微摩尔)和Nω-硝基-L-精氨酸(L-NOArg,100微摩尔)显著降低了触发肠道排空所需的阈值体积。L-精氨酸(4毫摩尔)可逆转这种作用,且单独使用L-精氨酸会增加蠕动起始的阈值体积。产生一氧化氮的硝普钠(0.1 - 10微摩尔)也会增加阈值体积。L-NAME、L-NOArg、L-精氨酸和硝普钠不会改变排空过程中产生的最大管腔内压力。L-NAME和L-NOArg显著增加了液体注入初始阶段纵向肌的收缩,而硝普钠(1纳摩尔至10微摩尔)则使其降低。4. 蜂毒明肽(0.5微摩尔)不会显著改变启动蠕动或纵向肌收缩所需的阈值体积。然而,肠道排空时产生的最大压力显著增加。此外,在触发蠕动性排空之前,短段环形肌明显随机收缩。5. L-NAME和蜂毒明肽的组合完全破坏了蠕动。环形肌的收缩并不总是从口腔端开始。观察到了静止收缩以及向口腔和肛门传播的收缩。6. 得出的结论是,肠内抑制性运动神经元对于蠕动的发生至关重要。它们通过一氧化氮在设定触发蠕动性排空的阈值方面很重要。它们通过一种对蜂毒明肽敏感的传递机制对于环形肌收缩的传播至关重要。蠕动过程中纵向肌的收缩部分受到一氧化氮介导机制的抑制。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16ba/1155610/5d6ec0b4c746/jphysiol00350-0095-a.jpg

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