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离体灌注人胰腺中内脏神经对生长抑素分泌的调节

Splanchnic neural regulation of somatostatin secretion in the isolated perfused human pancreas.

作者信息

Brunicardi F C, Elahi D, Andersen D K

机构信息

Department of Surgery and Medicine, State University of New York, Health Science Center at Brooklyn.

出版信息

Ann Surg. 1994 Mar;219(3):258-66. doi: 10.1097/00000658-199403000-00005.

Abstract

OBJECTIVE

The somatostatin-secreting delta cells in the islets of Langerhans appear to be regulated by neural mechanisms that have not been defined clearly. In this study, the celiac neural bundle of the human pancreas was electrically stimulated in the presence and absence of selective neural antagonists.

SUMMARY BACKGROUND DATA

The authors previously reported on studies of the splanchnic neural regulation of insulin, glucagon, and pancreatic polypeptide secretion. In these studies, alpha-adrenergic fibers appeared to have a predominant effect, strongly inhibiting the secretion of insulin, glucagon, and pancreatic polypeptide secretion. Cholinergic fibers appeared to stimulate strongly, although beta-adrenergic fibers weakly stimulated, the secretion of these hormones. Investigations of neural regulatory mechanisms governing human somatostatin release in vitro have not been previously reported.

METHODS

Pancreata were obtained from eight cadaveric organ donors. The isolated perfused human pancreas technique was used to assess the regulation of somatostatin secretion by the various neural fibers contained within the celiac plexus. The secretory response of somatostatin was examined in the presence of 16.7 mmol/L glucose, with and without neural stimulation, and specific neural antagonists.

RESULTS

The basal somatostatin secretion was 88 +/- 26 fmol/g/min and increased 131 +/- 23% (n = 8, p < 0.01) in response to 16.7 mmol/L glucose. The augmentation seen with glucose was inhibited 66 +/- 22% (n = 8, p < 0.05) during celiac neural bundle stimulation. Alpha-adrenergic blockade resulted in a 90 +/- 30% (n = 6, p < 0.01) augmentation of somatostatin release. Beta-adrenergic blockade caused a 13 +/- 2% (n = 6, p < 0.05) suppression of somatostatin release. Complete adrenergic blockade resulted in a 25 +/- 23% (n = 5, p = not significant) inhibition of somatostatin release. Cholinergic blockade resulted in a 40 +/- 10% (n = 6, p < 0.02) suppression of somatostatin release.

CONCLUSIONS

The predominant effect of celiac neural bundle stimulation was inhibition of somatostatin secretion through an alpha-adrenergic effect. Beta-adrenergic fibers stimulate somatostatin secretion; cholinergic fibers have a negligible effect on somatostatin secretion. These data suggest that the splanchnic innervation of the pancreas has a potent regulatory role in somatostatin release in this in vitro human model.

摘要

目的

胰岛中分泌生长抑素的δ细胞似乎受尚未明确界定的神经机制调控。在本研究中,在存在和不存在选择性神经拮抗剂的情况下,对人胰腺的腹腔神经束进行电刺激。

总结背景数据

作者之前报道过有关内脏神经对胰岛素、胰高血糖素和胰多肽分泌调节的研究。在这些研究中,α-肾上腺素能纤维似乎具有主要作用,强烈抑制胰岛素、胰高血糖素和胰多肽的分泌。胆碱能纤维似乎有强烈刺激作用,而β-肾上腺素能纤维对这些激素的分泌有微弱刺激作用。此前尚未有关于体外调控人生长抑素释放的神经调节机制的研究报道。

方法

从8名尸体器官捐赠者获取胰腺。采用离体灌注人胰腺技术,评估腹腔丛内各种神经纤维对生长抑素分泌的调节作用。在存在16.7 mmol/L葡萄糖的情况下,分别在有和无神经刺激以及有特异性神经拮抗剂的条件下,检测生长抑素的分泌反应。

结果

基础生长抑素分泌量为88±26 fmol/g/分钟,在16.7 mmol/L葡萄糖刺激下增加131±23%(n = 8,p < 0.01)。腹腔神经束刺激期间,葡萄糖引起的生长抑素分泌增加被抑制66±22%(n = 8,p < 0.05)。α-肾上腺素能阻断导致生长抑素释放增加90±30%(n = 6,p < 0.01)。β-肾上腺素能阻断导致生长抑素释放减少13±2%(n = 6,p < 0.05)。完全肾上腺素能阻断导致生长抑素释放减少25±23%(n = 5,p = 无显著性差异)。胆碱能阻断导致生长抑素释放减少40±10%(n = 6,p < 0.02)。

结论

腹腔神经束刺激的主要作用是通过α-肾上腺素能效应抑制生长抑素分泌。β-肾上腺素能纤维刺激生长抑素分泌;胆碱能纤维对生长抑素分泌的影响可忽略不计。这些数据表明,在这个体外人模型中,胰腺的内脏神经支配在生长抑素释放中具有重要的调节作用。

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