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Neuroregulation by vasoactive intestinal peptide (VIP) of mucus secretion in ferret trachea: activation of BKCa channels and inhibition of neurotransmitter release

机译:雪貂气管粘液分泌的血管活性肠肽(VIP)对神经的调节:BKCa通道的激活和神经递质释放的抑制

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摘要

The aims of this study were to determine: (1) whether vasoactive intestinal peptide (VIP) regulates cholinergic and ‘sensory-efferent' (tachykininergic) 35SO4 labelled mucus output in ferret trachea in vitro, using a VIP antibody, (2) the class of potassium (K+) channel involved in VIP-regulation of cholinergic neural secretion using glibenclamide (an ATP-sensitive K+ (KATP) channel inhibitor), iberiotoxin (a large conductance calcium activated K+ (BKca) channel blocker), and apamin (a small conductance Kca (SKca) channel blocker), and (3) the effect of VIP on cholinergic neurotransmission using [3H]-choline overflow as a marker for acetylcholine (ACh) release.Exogenous VIP (1 and 10 μM) alone increased 35SO4 output by up to 53% above baseline, but suppressed (by up to 80% at 1 μM) cholinergic and tachykininergic neural secretion without altering secretion induced by ACh or substance P (1 μM each). Endogenous VIP accounted for the minor increase in non-adrenergic, non-cholinergic (NANC), non-tachykininergic neural secretion, which was compatible with the secretory response of exogenous VIP.Iberiotoxin (3 μM), but not apamin (1 μM) or glibenclamide (0.1 μM), reversed the inhibition by VIP (10 nM) of cholinergic neural secretion.Both endogenous VIP (by use of the VIP antibody; 1 : 500 dilution) and exogenous VIP (0.1 μM), the latter by 34%, inhibited ACh release from cholinergic nerve terminals and this suppression was completely reversed by iberiotoxin (0.1 μM).We conclude that, in ferret trachea in vitro, endogenous VIP has dual activity whereby its small direct stimulatory action on mucus secretion is secondary to its marked regulation of cholinergic and tachykininergic neurogenic mucus secretion. Regulation is via inhibition of neurotransmitter release, consequent upon opening of BKCa channels. In the context of neurogenic mucus secretion, we propose that VIP joins NO as a neurotransmitter of i-NANC nerves in ferret trachea.
机译:这项研究的目的是确定:(1)是否在体外使用VIP抗体调节血管活性肠肽(VIP)在雪貂气管中调节胆碱能和“感觉有效”(速激肽能)35SO4标记的粘液输出,(2) glibenclamide(一种ATP敏感的K +(KATP)通道抑制剂),iberiotoxin(一种大的电导钙激活的K +(BKca)通道阻滞剂)和apamin(一种小剂量)参与胆碱能神经分泌的VIP调节的钾(K +)通道(3)用[3H]-胆碱溢流作为乙酰胆碱(ACh)释放的标志物,VIP对胆碱能神经传递的影响。单独使用外源VIP(1和10μm)可增加35SO4的输出比基线高53%,但抑制胆碱能和速激肽神经分泌(在1μM时高达80%),而不会改变ACh或P物质(各1μM)诱导的分泌。内源性VIP占非肾上腺素,非胆碱能(NANC),非速激肽能神经分泌的小幅增加,与外源VIP的分泌反应相容:伊贝毒素(3μM),而不是apamin(1μM)或格列本脲(0.1μM)逆转VIP(10 nM)对胆碱能神经分泌的抑制作用,内源性VIP(1 use:; 500稀释度)和外源VIP(0.1μM)均被后者抑制34%,抑制胆碱能神经末梢释放乙酰胆碱,这种抑制作用被埃博毒素(0.1μμM)完全逆转。我们的结论是,在雪貂气管中,内源性VIP具有双重活性,其对粘液分泌的小的直接刺激作用是其显着调节的第二作用。胆碱能和速激肽能的神经源性粘液分泌。调节是通过抑制神经递质释放来实现的,因此是在BKCa通道打开后进行的。在神经源性粘液分泌的背景下,我们建议VIP加入NO作为雪貂气管中i-NANC神经的神经递质。

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