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孤啡肽通过抑制大鼠结肠中的嘌呤能通路引起收缩。

Orphanin FQ causes contractions via inhibiting purinergic pathway in the rat colon.

作者信息

Takahashi T, Bagnol D, Schneider D, Mizuta Y, Ishiguchi T, LePard K, Galligan J J, Watson S J, Owyang C

机构信息

Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Gastroenterology. 2000 Oct;119(4):1054-63. doi: 10.1053/gast.2000.18154.

Abstract

BACKGROUND & AIMS: We have previously shown that orphanin FQ (OFQ) preferentially stimulates muscle contraction in the rat colon. However, the mechanism of action of OFQ remains unclear.

METHODS

We studied the effects of OFQ on muscle contractions and inhibitory junction potentials (IJPs) in rat colon. The site of action of OFQ was also investigated by in situ hybridization of OFQ receptors.

RESULTS

OFQ (10(-10) to 10(-6) mol/L) caused circular muscle contractions that were blocked by tetrodotoxin (10(-7) mol/L), suggesting the contractions were nerve mediated. Suramin (a nonselective P(2)-purinoceptor antagonist; 10(-4) mol/L) and reactive blue 2 (a P(2Y)-purinoceptor antagonist; 3 x 10(-5) mol/L), but not pyridoxalphosphate-6-azophenyl-2',4' disulfonic acid (PPADS; a P(2X)-purinoceptor antagonist; 3 x 10(-5) mol/L), abolished OFQ-induced colonic contractions. Focal stimulation of interganglionic fiber tracts evoked biphasic IJPs in colonic circular muscle cells. Suramin and reactive blue 2 inhibited the peak amplitude of the IJP, whereas PPADS had no effect. Cumulative addition of OFQ (10(-10) to 10(-6 )mol/L) significantly inhibited the IJPs. In situ hybridization revealed that OFQ receptor messenger RNA was expressed in the colonic myenteric plexus but not in the smooth muscle cells, suggesting that the site of action of OFQ is neuronal.

CONCLUSIONS

These results suggest that OFQ causes muscle contractions by inhibiting purinergic inhibitory motorneurons in the rat colon.

摘要

背景与目的

我们之前已表明孤啡肽(OFQ)可优先刺激大鼠结肠的肌肉收缩。然而,OFQ的作用机制仍不清楚。

方法

我们研究了OFQ对大鼠结肠肌肉收缩和抑制性接头电位(IJPs)的影响。还通过OFQ受体的原位杂交研究了OFQ的作用位点。

结果

OFQ(10⁻¹⁰至10⁻⁶mol/L)引起环形肌收缩,该收缩被河豚毒素(10⁻⁷mol/L)阻断,提示该收缩是神经介导的。苏拉明(一种非选择性P₂-嘌呤受体拮抗剂;10⁻⁴mol/L)和反应性蓝2(一种P₂Y-嘌呤受体拮抗剂;3×10⁻⁵mol/L),但不是磷酸吡哆醛-6-偶氮苯-2',4'-二磺酸(PPADS;一种P₂X-嘌呤受体拮抗剂;3×10⁻⁵mol/L),可消除OFQ诱导的结肠收缩。对神经节间纤维束的局部刺激在结肠环形肌细胞中诱发双相IJPs。苏拉明和反应性蓝2抑制IJP的峰值幅度,而PPADS无作用。OFQ(10⁻¹⁰至10⁻⁶mol/L)的累积添加显著抑制IJPs。原位杂交显示OFQ受体信使核糖核酸在结肠肌间神经丛中表达,但不在平滑肌细胞中表达,提示OFQ的作用位点是神经元。

结论

这些结果表明OFQ通过抑制大鼠结肠中的嘌呤能抑制性运动神经元引起肌肉收缩。

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