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首页> 外文期刊>Journal of Molecular Neuroscience: MN >Prolonged Acetylsalicylic-Acid-Supplementation-Induced Gastritis Affects the Chemical Coding of the Stomach Innervating Vagal Efferent Neurons in the Porcine Dorsal Motor Vagal Nucleus (DMX)
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Prolonged Acetylsalicylic-Acid-Supplementation-Induced Gastritis Affects the Chemical Coding of the Stomach Innervating Vagal Efferent Neurons in the Porcine Dorsal Motor Vagal Nucleus (DMX)

机译:长时间的乙酰水杨酸补充诱导的胃炎影响猪背运动迷走神经核(DMX)的神经支配迷走神经传入神经元的化学编码。

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The main goal of our research was to study the possible alterations of the chemical coding of the dorsal motor vagal nucleus (DMX) neurons projecting to the porcine stomach prepyloric region following prolonged acetylsalicylic acid supplementation. Fast Blue (FB) was injected into the studied area of the stomach. Since the seventh day following the FB injection, acetylsalicylic acid (ASA) was given orally to the experimental gilts. All animals were euthanized on the 28th day after FB injection. Medulla oblongata sections were then processed for double-labeling immunofluorescence for choline acetyltransferase (ChAT), pituitary adenylate cyclase-activating peptide (PACAP), vasoactive intestinal polypeptide (VIP), nitric oxide synthase (NOS), galanin (GAL), substance P (SP), leu enkephalin (LENK), and cocaine- and amphetamine-regulated transcript (CART). In the control DMX, only PACAP was observed in 30.08 +/- 1.97 % of the FB-positive neurons, while VIP, NOS, GAL, SP, LENK, and CART were found exclusively in neuronal processes running between FB-labeled perikarya. In the ASA DMX, PACAP was revealed in 49.53 +/- 5.73 % of traced vagal perikarya. Moreover, we found de novo expression of VIP in 40.32 +/- 7.84 %, NOS in 25.02 +/- 6.08 %, and GAL in 3.37 +/- 0.85 % of the FB-labeled neurons. Our results suggest that neuronal PACAP, VIP, NOS, and GAL are mediators of neural response to aspirin-induced stomach inflammatory state.
机译:我们研究的主要目的是研究长时间补充乙酰水杨酸后,投射到猪胃前幽门区域的背运动迷走神经核(DMX)神经元化学编码的可能变化。将鲜蓝色(FB)注入胃的研究区域。自从FB注射后的第七天开始,对实验小母猪口服乙酰水杨酸(ASA)。 FB注射后第28天将所有动物安乐死。然后处理延髓切片,对胆碱乙酰转移酶(ChAT),垂体腺苷酸环化酶激活肽(PACAP),血管活性肠多肽(VIP),一氧化氮合酶(NOS),甘丙肽(GAL),物质P( SP),亮脑啡肽(LENK)以及可卡因和苯丙胺调节的转录本(CART)。在对照DMX中,在30.08 +/- 1.97%的FB阳性神经元中仅观察到PACAP,而VIP,NOS,GAL,SP,LENK和CART仅在FB标记的近核之间的神经元过程中发现。在ASA DMX中,有49.53 +/- 5.73%的迷走性眼周核被暴露出PACAP。此外,我们发现在FB标记的神经元中,VIP的从头表达为40.32 +/- 7.84%,NOS为25.02 +/- 6.08%,GAL为3.37 +/- 0.85%。我们的结果表明,神经元PACAP,VIP,NOS和GAL是对阿司匹林诱发的胃部炎症状态的神经反应的介体。

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