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Aspirin Administration Affects Neurochemical Characterization of Substance P-Like Immunoreactive (SP-LI) Nodose Ganglia Neurons Supplying the Porcine Stomach

机译:阿司匹林给药影响物质的p样子的神经化学表征(SP-Li)乳晕胃的核糖神经节神经元

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摘要

Background. Acetylsalicylic acid (ASA) is a commonly used anti-inflammatory, antipyretic, and analgesic drug, which has many side effects on the gastric mucosal layer. Despite this, knowledge concerning the influence of ASA on neuronal cells supplying the stomach is very scanty. Methods. This investigation was performed on ten immature gilts of the Large White Polish race divided into two groups (five animals in each): a control group and animals which were treated with ASA. The retrograde neuronal tracer Fast Blue (FB) was injected into the prepyloric region of the stomach in all animals. ASA was then given orally to the experimental (ASA) group of gilts from the seventh day after FB injection to the 27th day of the experiment. After this period, all animals were euthanized. Immediately after euthanasia, nodose ganglia (NG) were collected and subjected to a standard double-labelling immunofluorescence technique using antibodies directed toward substance P (SP) and other selected neuronal factors, such as galanin (GAL), neuronal isoform of nitric oxide synthase (nNOS), vasoactive intestinal polypeptide (VIP), and calcitonin gene-related peptide (CGRP). Key Results. The obtained results show that SP-LI neurons located in NG supplying the porcine stomach were also immunoreactive to all the above-mentioned neuronal factors. Moreover, ASA administration caused an increase in the degree of colocalization of SP with other neuronal active substances, and the most visible changes concerned the number of neurons simultaneously immunoreactive to SP and CGRP. Conclusions and Inferences. These observations indicate that the population of SP-LI neurons supplying the stomach is not homogeneous and may undergo changes after ASA administration. These changes are probably connected with inflammatory processes and/or neuroprotective reactions although their exact mechanisms remain unknown.
机译:背景。乙酰胱氨酸(ASA)是常用的抗炎,解热和镇痛药,其对胃粘膜层具有许多副作用。尽管如此,关于供给胃的神经元细胞对asa的影响的知识非常稀少。方法。这项调查是对大型白波兰种族的十个未成熟肠道进行的调查,分为两组(每组五只动物):用ASA处理的对照组和动物。将逆行神经元示踪剂快蓝(FB)注入胃中的所有动物的胃部区域。然后在FB注射术后第七天对实验(ASA)Gilts进行口服给予实验(ASA)吉尔特。在此之后,所有动物都被安乐死。在安乐死之后,使用朝向物质P(SP)和其他所选神经元因子的抗体收集Nodose Ganglia(NG)并进行标准的双标记免疫荧光技术,例如环肽(GAL),一氧化氮合酶的神经元同种型( NNOS),血管活性肠多肽(VIP)和Calcitonin基因相关肽(CGRP)。关键结果。所得结果表明,位于NG的SP-Li神经元供应猪胃也对所有上述神经元因子进行免疫反应。此外,ASA施用导致SP与其他神经元活性物质的分层程度的增加,并且最明显的变化涉及与SP和CGRP同时免疫激素的神经元数。结论和推论。这些观察结果表明,供应胃的SP-Li神经元的群体不是均匀的,可能在ASA给药后进行变化。这些变化可能与炎症过程和/或神经保护反应相关,尽管它们的确切机制仍然未知。

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