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胰多肽对大鼠迷走神经背核复合体神经元的作用。

Effect of pancreatic polypeptide on rat dorsal vagal complex neurons.

作者信息

McTigue D M, Hermann G E, Rogers R C

机构信息

Department of Physiology, College of Medicine, Ohio State University, Columbus 43210, USA.

出版信息

J Physiol. 1997 Mar 1;499 ( Pt 2)(Pt 2):475-83. doi: 10.1113/jphysiol.1997.sp021942.

Abstract
  1. Pancreatic polypeptide (PP) microinjected into the dorsal vagal complex (DVC) elevates gastric activity through a vagal mechanism. Thus, it was hypothesized that PP alters the activity of nuclei comprising the DVC, i.e. the nucleus tractus solitarii (NTS) and the dorsal motor nucleus (DMN). 2. In vivo and in vitro approaches were used. For in vivo studies, micropipettes were used for recording and injecting vehicle or PP. Neurons were identified as NTS or DMN using orthodromic and antidromic activation, respectively, following vagal stimulation. Gastric-related DVC neurons were located using antral inflation. For in vitro studies, DMN neurons were recorded from medullary slices. 3. Of the twenty-eight NTS and DMN neurons identified, fifteen were activated, six inhibited and seven unaffected after PP microinjection. Forty-two gastric-related neurons were located in the DVC, of which twenty-five were stimulated by PP and seventeen exhibited no change. No gastric-related cells were inhibited. 4. For in vitro studies, 66% of DMN neurons were activated by PP (n = 27/47) while the remaining 33% were inhibited (n = 14/47). Similar results were obtained in normal or synaptic blockade media. 5. These results support the hypothesis that PP alters DVC neuronal activity, which may thereby lead to the previously observed alterations in gastric activity.
摘要
  1. 微量注射到迷走神经背侧复合体(DVC)的胰多肽(PP)通过迷走神经机制提高胃活动。因此,有人提出假说,PP会改变构成DVC的核团即孤束核(NTS)和迷走神经背核(DMN)的活动。2. 使用了体内和体外研究方法。对于体内研究,使用微量移液器记录并注射载体或PP。在迷走神经刺激后,分别使用顺行和逆行激活将神经元鉴定为NTS或DMN。通过胃窦扩张定位与胃相关的DVC神经元。对于体外研究,从延髓切片记录DMN神经元。3. 在鉴定出的28个NTS和DMN神经元中,微量注射PP后,15个被激活,6个被抑制,7个未受影响。在DVC中定位到42个与胃相关的神经元,其中25个受到PP刺激,17个无变化。没有与胃相关的细胞被抑制。4. 对于体外研究,66%的DMN神经元被PP激活(n = 27/47),而其余33%被抑制(n = 14/47)。在正常或突触阻断培养基中获得了类似结果。5. 这些结果支持了PP改变DVC神经元活动的假说,这可能进而导致先前观察到的胃活动改变。

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