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向大鼠蓝斑/蓝斑下核微量注射促肾上腺皮质激素释放因子可通过脊髓途径抑制胃酸分泌。

Microinfusion of corticotropin-releasing factor into the locus coeruleus/subcoeruleus nuclei inhibits gastric acid secretion via spinal pathways in the rat.

作者信息

Mönnikes H, Tebbe J, Bauer C, Lauer G, Arnold R

机构信息

Department of Internal Medicine, Philipps-University of Marburg, Germany.

出版信息

Brain Res. 1996 Jul 29;728(2):157-65. doi: 10.1016/0006-8993(96)00393-9.

Abstract

Brain corticotropin-releasing factor (CRF) is involved in stress-related alterations of gastric acid secretion. CRF in the locus coeruleus has been shown to induce anxiogenic behavioral responses and to mimic stress-induced alterations of colonic motor function. Whether the locus coeruleus/subcoeruleus nucleus (LC/SC) is a site of action for CRF to alter gastric acid secretion was investigated in urethane-anesthetized gastric fistula rats. In sham-operated animals, CRF (126-420 pmol) microinfused bilaterally into the LC/SC induced a dose-dependent inhibition of pentagastrin (PG)-stimulated gastric acid secretion of 60-81% within the first hour after microinjection. At the 420 pmol dose, this inhibitory effect of CRF into the LC/SC lasted throughout the whole observation period of 120 min. After bilateral vagotomy, basal and PG-stimulated gastric acid secretion at microinjection of vehicle was reduced. Nevertheless, microinfusion of 420 pmol CRF into the LC/SC still inhibited significantly gastric acid secretion by 62.1%. In contrast, in spinal cord transected animals bilateral microinfusion of 420 pmol CRF into the LC/SC did not reduce PG-stimulated gastric acid secretion. These data indicate that CRF acts in the LC/SC to induce a long lasting inhibition of peripherally stimulated gastric acid secretion via spinal pathways. These findings suggest a possible role of the LC/SC in the regulation of gastric secretion and of endogenous CRF at these sites in the stress-related inhibition of gastric acid secretion by affecting autonomic nervous system activity.

摘要

脑促肾上腺皮质激素释放因子(CRF)参与胃酸分泌的应激相关改变。蓝斑中的CRF已被证明可诱导焦虑行为反应,并模拟应激诱导的结肠运动功能改变。在乌拉坦麻醉的胃瘘大鼠中,研究了蓝斑/蓝斑下核(LC/SC)是否是CRF改变胃酸分泌的作用部位。在假手术动物中,双侧微量注射到LC/SC中的CRF(126 - 420 pmol)在注射后的第一小时内对五肽胃泌素(PG)刺激的胃酸分泌产生60 - 81%的剂量依赖性抑制。在420 pmol剂量下,CRF对LC/SC的这种抑制作用在整个120分钟的观察期内持续存在。双侧迷走神经切断术后,注射溶媒时的基础胃酸分泌和PG刺激的胃酸分泌均减少。然而,向LC/SC中微量注射420 pmol CRF仍能显著抑制胃酸分泌62.1%。相反,在脊髓横断的动物中,双侧向LC/SC中微量注射420 pmol CRF并未降低PG刺激的胃酸分泌。这些数据表明,CRF通过脊髓途径在LC/SC中发挥作用,诱导对周围刺激的胃酸分泌产生持久抑制。这些发现提示LC/SC在胃酸分泌调节以及应激相关胃酸分泌抑制中通过影响自主神经系统活动,对这些部位内源性CRF可能具有一定作用。

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