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Peristalsis is impaired in the small intestine of mice lacking the P2X3 subunit

机译:缺少P2X3亚基的小鼠小肠蠕动受损

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摘要

P2X receptors are ATP-gated cation channels composed of one or more of seven different subunits. P2X receptors participate in intestinal neurotransmission but the subunit composition of enteric P2X receptors is unknown. In this study, we used tissues from P2X3 wild-type (P2X3+/+) mice and mice in which the P2X3 subunit gene had been deleted (P2X3−/−) to investigate the role of this subunit in neurotransmission in the intestine. RT-PCR analysis of mRNA from intestinal tissues verified P2X3 gene deletion. Intracellular electrophysiological methods were used to record synaptic and drug-induced responses from myenteric neurons in vitro. Drug-induced longitudinal muscle contractions were studied in vitro. Intraluminal pressure-induced reflex contractions (peristalsis) of ileal segments were studied in vitro using a modified Trendelenburg preparation. Gastrointestinal transit was measured as the progression in 30 min of a liquid radioactive marker administered by gavage to fasted mice. Fast excitatory postsynaptic potentials recorded from S neurons (motoneurons and interneurons) were similar in tissues from P2X3+/+ and P2X3−/− mice. S neurons from P2X3+/+ and P2X3−/− mice were depolarized by application of ATP but not α,β-methylene ATP, an agonist of P2X3 subunit-containing receptors. ATP and α,β-methylene ATP induced depolarization of AH (sensory) neurons from P2X3+/+ mice. ATP, but not α,β-methylene ATP, caused depolarization of AH neurons from P2X3−/− mice. Peristalsis was inhibited in ileal segments from P2X3−/− mice but longitudinal muscle contractions caused by nicotine and bethanechol were similar in segments from P2X3+/+ and P2X3−/− mice. Gastrointestinal transit was similar in P2X3+/+ and P2X3−/− mice. It is concluded that P2X3 subunit-containing receptors participate in neural pathways underlying peristalsis in the mouse intestine in vitro. P2X3 subunits are localized to AH (sensory) but not S neurons. P2X3 receptors may contribute to detection of distention or intraluminal pressure increases and initiation of reflex contractions.
机译:P2X受体是由七个不同亚基中的一个或多个组成的ATP门控阳离子通道。 P2X受体参与肠道神经传递,但肠P2X受体的亚基组成尚不清楚。在这项研究中,我们使用了来自P2X3野生型(P2X3 + / + )小鼠和已删除P2X3亚基基因的小鼠的组织(P2X3 -/-)研究该亚基在肠道神经传递中的作用。肠道组织中mRNA的RT-PCR分析证实了P2X3基因的缺失。细胞内电生理学方法被用于记录肌膜神经元在体外的突触和药物诱导的反应。在体外研究了药物诱导的纵向肌肉收缩。使用改良的特伦德伦伯卧位制剂体外研究回肠段的腔内压力诱导的反射收缩(蠕动)。胃肠运输是通过强饲禁食小鼠在30分钟内液态放射性标记物的进展来衡量的。在P2X3 + / + 和P2X3 -/-小鼠的组织中,从S神经元(运动神经元和中间神经元)记录的快速兴奋性突触后电位相似。 P2X3 + / + 和P2X3 -/-小鼠的S神经元通过ATP消极化,但不使用α,β-亚甲基ATP(含P2X3亚基受体的激动剂)去极化。 ATP和α,β-亚甲基ATP诱导P2X3 + / + 小鼠AH(感觉)神经元去极化。 ATP引起P2X3 -/-小鼠AH神经元的去极化,但不是α,β-亚甲基ATP。在P2X3 -/-小鼠的回肠段中,蠕动受到抑制,但是在P2X3 + / + 和P2X3 -中,尼古丁和苯乙二酚引起的纵向肌肉收缩相似/ − 小鼠。 P2X3 + / + 和P2X 3 -/-小鼠的胃肠道转运相似。结论:P2X 3 亚基受体参与体外小鼠肠蠕动的神经通路。 P2X 3 亚基定位于AH(感觉)而不是S神经元。 P2X 3 受体可能有助于发现扩张或管腔内压力升高以及反射性收缩的开始。

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