Manning Brian P, Sharkey Keith A, Mawe Gary M
Department of Anatomy and Neurobiology, University of Vermont College of Medicine, Burlington, Vermont 05405, USA.
Am J Physiol Gastrointest Liver Physiol. 2002 Dec;283(6):G1388-97. doi: 10.1152/ajpgi.00141.2002. Epub 2002 Aug 21.
PGE(2) is a proinflammatory mediator that can influence many cell types. This study was conducted to determine whether PGE(2) alters the electrical activity of distal colonic myenteric neurons, because colitis is typically associated with altered motility and changes in neural signaling may be involved. The electrical properties of intact myenteric neurons were evaluated with intracellular microelectrodes. Acute application of PGE(2) elicited a prolonged depolarization in both AH and S neurons with little effect on input resistance or electrical excitability. PGE(2) effects were suppressed by tetrodotoxin (TTX) or neurokinin (NK) receptor antagonists, indicating that PGE(2) acts directly and indirectly to depolarize colonic neurons. PGE(2)-evoked depolarization was concentration dependent (approximately 3 microM EC(50)) and was attenuated by the E prostanoid (EP)1/2 receptor antagonist, AH-6809. When preparations were maintained for 48 h in the presence of the stable PGE(2) analog PGE(2)-ethanolamide (10 microM), neurons exhibited a significant membrane depolarization and enhanced excitability. These results suggest that PGE(2) can play a role in altered motility in colitis by evoking changes in the electrical properties of myenteric neurons.
前列腺素E2(PGE(2))是一种促炎介质,可影响多种细胞类型。本研究旨在确定PGE(2)是否会改变远端结肠肌间神经元的电活动,因为结肠炎通常与运动改变有关,且可能涉及神经信号的变化。用细胞内微电极评估完整肌间神经元的电特性。急性应用PGE(2)可使AH神经元和S神经元出现长时间去极化,对输入电阻或电兴奋性影响较小。PGE(2)的作用被河豚毒素(TTX)或神经激肽(NK)受体拮抗剂抑制,表明PGE(2)直接和间接作用使结肠神经元去极化。PGE(2)诱发的去极化呈浓度依赖性(约3 microM EC(50)),并被前列环素(EP)1/2受体拮抗剂AH-6809减弱。当在稳定的PGE(2)类似物PGE(2)-乙醇酰胺(10 microM)存在下将标本维持48小时时,神经元表现出明显的膜去极化和兴奋性增强。这些结果表明,PGE(2)可通过引起肌间神经元电特性的变化在结肠炎的运动改变中发挥作用。