首页> 外文期刊>American Journal of Physiology >Secretin inhibits gastric acid secretion via a vagal afferent pathway in rats.
【24h】

Secretin inhibits gastric acid secretion via a vagal afferent pathway in rats.

机译:促胰液素通过大鼠的迷走神经传入途径抑制胃酸分泌。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Secretin is an enterogastrone that inhibits gastric acid secretion and motility. Recently, it was reported that secretin inhibited gastric emptying via a capsaicin (Cap)-sensitive vagal afferent pathway. However, a possible role of the sensory afferent pathway in secretin-inhibited acid secretion has not been clarified. We investigated whether or not the acid secretion suppressed by secretin is modulated by a vagal and/or splanchnic afferent pathway in rats. Subdiaphragmatic perivagal (PV) or periceliac ganglionic (PCG) application of Cap (10 mg/ml) or vehicle was performed in both conscious and anesthetized rats 2 wk before experiments. Bilateral vagotomy was performed in some conscious rats 5 days before studies. Pentagastrin was administered intravenously at 0.6 microg . kg-1 . h-1. Secretin (20 pmol . kg-1 . h-1 iv) or 0.03 N HCl (4.32 ml/h id) was infused in conscious rats with gastric cannulas or anesthetized rats with ligation of the pylorus, respectively. A rabbit antisecretin serum was injected in some anesthetized rats before duodenal acidification. Secretin significantly inhibited pentagastrin-stimulated acid secretion by 63% (P < 0.01), which was abolished by both vagotomy and PV treatment of Cap in conscious rats. In anesthetized rats, duodenal infusion of 0.03 N HCl suppressed pentagastrin-induced acid secretion by 59.4% (P < 0.01), which was reversed not only by antisecretin serum but also by PV application of Cap. However, PCG treatment with Cap did not influence the inhibition by secretin or duodenal acidification in either awake or anesthetized rats. These results indicate that the inhibition by secretin of pentagastrin-stimulated acid secretion is mediated by a Cap-sensitive vagal afferent pathway but not via a splanchnic afferent pathway in rats.
机译:促胰液素是抑制胃酸分泌和运动的肠胃泌素。最近,据报道,促胰液素通过辣椒素(Cap)敏感的迷走神经传入途径抑制胃排空。然而,尚未阐明感觉传入途径在促胰液素抑制的酸分泌中的可能作用。我们研究了分泌素抑制的酸分泌是否受到大鼠迷走神经和/或内脏传入通路的调节。实验前2周,在清醒和麻醉的大鼠中进行Cap(10 mg / ml)的dia下腹膜(PV)或腹膜神经节(PCG)施用。研究前5天,在一些清醒的大鼠中进行了双侧迷走神经切断术。五肽胃泌素静脉注射0.6微克。千克-1。 h-1。分别在清醒的胃插管大鼠或幽门结扎的麻醉大鼠中注入促胰液素(20 pmol。kg-1。h-1 iv)或0.03 N HCl(4.32 ml / h id)。在十二指肠酸化之前,在一些麻醉的大鼠中注射兔抗分泌素血清。促胰液素显着抑制五肽胃泌素刺激的酸分泌63%(P <0.01),这在意识清醒的大鼠中通过迷走神经切断术和Cap的PV治疗均被取消。在麻醉的大鼠中,十二指肠输注0.03 N HCl可抑制五肽胃泌素诱导的酸分泌59.4%(P <0.01),不仅抗分泌蛋白血清逆转,而且PV应用Cap逆转。然而,在清醒或麻醉的大鼠中,用Cap进行PCG治疗并不会影响促胰液素或十二指肠酸化的抑制作用。这些结果表明在大鼠中,分泌素对五肽胃泌素刺激的酸分泌的抑制是通过Cap敏感迷走神经传入途径介导的,而不是通过内脏传入途径介导的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号