首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of epithelium removal on relaxation of airway smooth muscle induced by vasoactive intestinal peptide and electrical field stimulation.
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Effects of epithelium removal on relaxation of airway smooth muscle induced by vasoactive intestinal peptide and electrical field stimulation.

机译:去除上皮对血管活性肠肽和电场刺激引起的气道平滑肌松弛的影响。

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摘要

1. We have studied the effect of epithelium removal on relaxation of guinea-pig isolated tracheal smooth muscle induced by vasoactive intestinal peptide (VIP) or stimulation of non-adrenergic, non-cholinergic (NANC) inhibitory nerves. Also examined were the effects of inhibitors of neutral endopeptidase (NEP) and angiotensin-converting enzyme (ACE). 2. Epithelium removal produced a 3.6 +/- 0.4 fold leftward shift in the VIP concentration-response curve. The supersensitivity to VIP, following epithelium removal was abolished by phosphoramidon or thiorphan (NEP inhibitors), but unaffected by captopril (an ACE inhibitor). In intact trachea, the NEP inhibitors produced leftward shifts in the VIP curves similar to those produced by epithelium removal. 3. In contrast to responses to exogenous VIP, neurogenic NANC inhibitory responses to electrical field stimulation were affected neither by epithelial denudation nor by the peptidase inhibitors. 4. As in previous studies, epithelium removal increased tracheal sensitivity to isoprenaline. This was not altered by pretreatment with a cocktail of peptidase inhibitors. Thus, the effect of the NEP inhibitors on responses to VIP appears to be relatively specific. 5. These data indicate that exogenous VIP is a substrate for airway NEP, since inhibition of the enzyme potentiates the peptide. This is further evidence that the airway epithelium provides a source for the metabolism of mediators. 6. In guinea-pig trachea the NEP responsible for cleaving VIP may be located largely in the epithelial layer, since NEP inhibition was without effect on sensitivity to VIP in epithelium-denuded preparations. If VIP is a NANC inhibitory neurotransmitter in this tissue its degradation endogenously does not appear to involve epithelial NEP.
机译:1.我们研究了上皮去除对血管活性肠肽(VIP)或非肾上腺素,非胆碱能(NANC)抑制神经刺激引起的豚鼠离体的气管平滑肌松弛的影响。还检查了中性内肽酶(NEP)和血管紧张素转换酶(ACE)抑制剂的作用。 2.去除上皮在VIP浓度-响应曲线中产生了3.6 +/- 0.4倍的向左移位。上皮去除后,对VIP的超敏性已被磷酰胺或噻菌灵(NEP抑制剂)消除,但不受卡托普利(ACE抑制剂)的影响。在完整的气管中,NEP抑制剂在VIP曲线中产生的左移类似于上皮去除所产生的。 3.与对外源VIP的反应相反,对电场刺激的神经源性NANC抑制反应既不受上皮剥脱也不受肽酶抑制剂的影响。 4.如以前的研究一样,上皮去除增加了气管对异丙肾上腺素的敏感性。用肽酶抑制剂混合物预处理并不能改变这一点。因此,NEP抑制剂对VIP应答的作用似乎是相对特异性的。 5.这些数据表明,外源VIP是气道NEP的底物,因为酶的抑制增强了该肽。这进一步证明气道上皮提供了介体代谢的来源。 6.在豚鼠气管中,负责裂解VIP的NEP可能主要位于上皮层,因为NEP抑制对上皮裸露制剂对VIP的敏感性没有影响。如果VIP是该组织中的NANC抑制神经递质,则其内源性降解似乎不涉及上皮NEP。

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