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通过向狗体内输注去甲肾上腺素对胰腺激素分泌进行体内刺激。

In vivo stimulation of pancreatic hormone secretion by norepinephrine infusion in the dog.

作者信息

Ribes G, Trimble E R, Blayac J P, Wollheim C B, Loubatières-Mariani M M

出版信息

Am J Physiol. 1984 Apr;246(4 Pt 1):E339-43. doi: 10.1152/ajpendo.1984.246.4.E339.

Abstract

Norepinephrine is generally regarded as an inhibitor of insulin release. It has been shown, however, that under hyperglycemic circumstances, norepinephrine infused at a high dose may also stimulate insulin secretion. The goals of this study were, under normoglycemic conditions, to confirm this stimulatory effect and to determine whether a beta-adrenergic mechanism or central neural pathways were involved. Secretion of pancreatic somatostatin and glucagon were also studied. Fasted, anesthetized dogs had norepinephrine (2 micrograms X kg-1 X min-1) infused into a peripheral vein for 60 min; blood was sampled from the pancreaticoduodenal vein. Norepinephrine stimulated insulin, somatostatin, and glucagon secretion without significant changes in either blood glucose concentration or pancreaticoduodenal venous blood flow. The stimulatory effect of norepinephrine on the three hormones was abolished by propranolol pretreatment, thus implicating a beta-adrenergic mechanism. Because bilateral cervical vagotomy prevented stimulation of insulin secretion by norepinephrine, central neural pathways must have been involved in the stimulatory process. However, norepinephrine-induced glucagon secretion was not decreased by vagotomy, showing that the stimulation was due to either a direct action on the pancreatic A cell or of a central pathway not mediated via the vagus nerve. Norepinephrine-induced somatostatin secretion was partly reduced by vagotomy, indicating that several mechanisms could be implicated.

摘要

去甲肾上腺素通常被认为是胰岛素释放的抑制剂。然而,已有研究表明,在高血糖情况下,高剂量注入的去甲肾上腺素也可能刺激胰岛素分泌。本研究的目的是在血糖正常的条件下,证实这种刺激作用,并确定是否涉及β-肾上腺素能机制或中枢神经通路。同时还研究了胰腺生长抑素和胰高血糖素的分泌。将禁食、麻醉的狗的外周静脉注入去甲肾上腺素(2微克·千克⁻¹·分钟⁻¹),持续60分钟;从胰十二指肠静脉取血样。去甲肾上腺素刺激了胰岛素、生长抑素和胰高血糖素的分泌,而血糖浓度和胰十二指肠静脉血流量均无显著变化。普萘洛尔预处理消除了去甲肾上腺素对这三种激素的刺激作用,因此提示存在β-肾上腺素能机制。由于双侧颈迷走神经切断术可阻止去甲肾上腺素对胰岛素分泌的刺激,因此中枢神经通路必定参与了这一刺激过程。然而,迷走神经切断术并未降低去甲肾上腺素诱导的胰高血糖素分泌,表明这种刺激是由于对胰腺A细胞的直接作用或不通过迷走神经介导的中枢通路所致。迷走神经切断术使去甲肾上腺素诱导的生长抑素分泌部分减少,表明可能涉及多种机制。

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