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Acetylcholine regulates glucagon secretion from human glucagonoma cells.

作者信息

Funakoshi A, Yasunami Y, Ryu S, Shinozaki H, Jimi A, Ikeda S

机构信息

Department of Gastroenterology, National Kyushu Cancer Center, Fukuoka, Japan.

出版信息

J Gastroenterol. 1994 Dec;29(6):797-9. doi: 10.1007/BF02349291.

DOI:10.1007/BF02349291
PMID:7874280
Abstract

Human glucagonoma cells were isolated and maintained in vitro. Incubation experiments showed that carbachol (Cch) induced the simultaneous release of glucagon, VIP (vasoactive intestinal polypeptide), and pancreatic polypeptide (PP) at levels significantly higher than basal levels. Atropine abolished the stimulatory effect of Cch on glucagon, VIP, and PP release. An immunohistological study of the tumor tissues revealed that the cells contained glucagon, VIP, and PP. These findings demonstrate, for the first time, the in vitro release of glucagon from glucagonoma cells by Cch stimulation.

摘要

相似文献

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本文引用的文献

1
In vitro release of vasoactive intestinal polypeptide and pancreatic polypeptide from human VIPoma cells and its inhibition by somatostatin analogue (SMS 201-995).血管活性肠肽和胰多肽从人血管活性肠肽瘤细胞的体外释放及其受生长抑素类似物(SMS 201-995)的抑制作用
Surgery. 1994 Jun;115(6):713-7.
2
Pancreatic polypeptide: a hormone under vagal control.胰多肽:一种受迷走神经控制的激素。
Gastroenterology. 1983 Dec;85(6):1411-25.
3
In vitro study of cultured human insulinoma cells: evidence of abnormal sensitivity to glucose.
J Clin Endocrinol Metab. 1987 Jul;65(1):110-5. doi: 10.1210/jcem-65-1-110.
4
Plasma cholecystokinin and pancreatic polypeptide responses after ingestion of a liquid test meal rich in medium-chain fatty acids in patients with chronic pancreatitis.慢性胰腺炎患者摄入富含中链脂肪酸的液体试验餐后血浆胆囊收缩素和胰多肽的反应
Am J Clin Nutr. 1989 Feb;49(2):247-51. doi: 10.1093/ajcn/49.2.247.
5
A case of multiple endocrine neoplasia (MEN) type 1; the immunohistochemical and ultrastructural studies of its tumors and the analysis of hormones in tumor extracts.1例1型多发性内分泌肿瘤(MEN);对其肿瘤的免疫组织化学和超微结构研究以及肿瘤提取物中的激素分析。
Endocrinol Jpn. 1989 Feb;36(1):37-45. doi: 10.1507/endocrj1954.36.37.