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神经降压素在大鼠胰腺中的作用部位。

The site of action of neurotensin in the rat pancreas.

作者信息

Feurle G E, Niestroj S

机构信息

Medizinische Poliklinik, University of Heidelberg, West Germany.

出版信息

Pancreas. 1991 Mar;6(2):202-7. doi: 10.1097/00006676-199103000-00012.

Abstract

The tridecapeptide neurotensin, present in endocrine cells of the ileal mucosa and in nerve bodies of cerebral nuclei, may play a role in the physiology of exocrine pancreatic regulation. This assumption is based on two observations: Neurotensin appears in the blood stream after a fatty meal and neurotensin stimulates exocrine pancreatic secretion. There has, however, been controversy on the site of action of this peptide since some investigators did not observe an effect on the pancreas in vitro and suggested, therefore, an indirect, perhaps neural or even central site of action. In the present investigation, we compared the action of neurotensin on the exocrine pancreas in vivo in the anesthetized rat after intracerebroventricular (i.c.v.) injection and after i.v. infusion and in vitro after incubation of the pancreas in three different preparations: isolated dispersed acini, isolated lobuli, and isolated total pancreas. We found that i.c.v. application of neurotensin stimulated exocrine pancreatic secretion only when doses were applied that led to elevated peripheral plasma neurotensin levels. In vitro, the action of neurotensin was very weak and the optimal dose was integrity dependent; e.g., a concentration of 10(-4) and 10(-5) M neurotensin was necessary to stimulate amylase release from isolated acini, 10(-8) M neurotensin induced amylase release from isolates lobuli, and 10(-9) M neurotensin released amylase from the intact pancreas. Intravenously, neurotensin resulted in a greater amylase release over basal than in any of the in vitro experiments. We conclude that neurotensin acts directly on the pancreatic acini but that the sensitivity of the pancreas is greatly enhanced when the organ is intact and has normal neural and vascular communications.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

十三肽神经降压素存在于回肠黏膜的内分泌细胞和脑核的神经体中,可能在外分泌胰腺调节生理过程中发挥作用。这一假设基于两项观察结果:进食脂肪餐后神经降压素会出现在血流中,且神经降压素会刺激外分泌胰腺分泌。然而,关于该肽的作用位点一直存在争议,因为一些研究人员在体外未观察到对胰腺的影响,因此认为其作用位点是间接的,可能是神经甚至中枢性的。在本研究中,我们比较了神经降压素在脑室内(i.c.v.)注射和静脉输注后对麻醉大鼠体内外分泌胰腺的作用,以及在三种不同制剂中胰腺孵育后体外的作用:分离的分散腺泡、分离的小叶和分离的整个胰腺。我们发现,只有当应用导致外周血浆神经降压素水平升高的剂量时,脑室内注射神经降压素才会刺激外分泌胰腺分泌。在体外,神经降压素的作用非常微弱,最佳剂量依赖于完整性;例如,10(-4)和10(-5)M的神经降压素浓度是刺激分离腺泡释放淀粉酶所必需的,10(-8)M的神经降压素可诱导分离小叶释放淀粉酶,而10(-9)M的神经降压素可使完整胰腺释放淀粉酶。静脉注射时,神经降压素导致的淀粉酶释放量比基础水平高,且高于任何体外实验。我们得出结论,神经降压素直接作用于胰腺腺泡,但当器官完整且具有正常的神经和血管联系时,胰腺的敏感性会大大增强。(摘要截短至250字)

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