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胃肠肽——在病理生理学和疾病中的作用

Gastrointestinal peptides--rôle in pathophysiology and disease.

作者信息

Creutzfeldt W

出版信息

Scand J Gastroenterol Suppl. 1982;77:7-20.

PMID:6750831
Abstract

Progress in gut hormone research has considerably increased our knowledge in gastrointestinal physiology. However, this knowledge has not yet helped the understanding of common gastrointestinal diseases. A pathophysiological role of gut hormones has been established only for rare conditions This is because the clinical significance of the gut hormones is difficult to evaluate. Morphological and biochemical methods used in classical endocrinology can rarely be applied to gastrointestinal endocrinology because of the special design of the gut hormone system. Also gut hormones and autonomous nervous system overlap in their function. A defect of one system can be compensated by the other. Since the hormone-producing cells of the gut are stimulated by food ingestion, any functional or organic change of the digestive tract will alter gut hormone response. Accordingly, most changes of gut hormone levels are secondary. In some--apparently rare--instances such secondary changes contribute to the symptomatology of a pathological condition. In other instances gut hormone abnormalities mimic common diseases, thus demonstrating the heterogenecity of these conditions. More specific and reliable methods are needed to prove or to exclude the participation of gastrointestinal peptides in the pathogenesis of gastrointestinal disease. Gut peptides are an important link between nutrient entry and metabolism. This is realized by a hormonal gut factor (incretin) which augments glucose-induced insulin release. GIP is the most thoroughly investigated but not the only incretin. In addition, GIP seems to have direct effects on lipid metabolism. This would explain why fat releases more GIP than glucose. Except in the case of the metabolic hormones insulin and glucagon the therapeutic usefulness of gastrointestinal peptides has not yet been established.

摘要

肠道激素研究的进展极大地增加了我们对胃肠生理学的认识。然而,这些知识尚未有助于理解常见的胃肠疾病。肠道激素的病理生理作用仅在罕见疾病中得到证实。这是因为肠道激素的临床意义难以评估。由于肠道激素系统的特殊设计,经典内分泌学中使用的形态学和生化方法很少能应用于胃肠内分泌学。此外,肠道激素和自主神经系统在功能上相互重叠。一个系统的缺陷可以由另一个系统来补偿。由于肠道中产生激素的细胞受到食物摄入的刺激,消化道的任何功能或器质性变化都会改变肠道激素的反应。因此,大多数肠道激素水平的变化都是继发性的。在一些——显然罕见的——情况下,这种继发性变化会导致病理状况的症状。在其他情况下,肠道激素异常会模仿常见疾病,从而证明这些疾病的异质性。需要更具体、更可靠的方法来证明或排除胃肠肽在胃肠疾病发病机制中的参与。胃肠肽是营养物质摄入与代谢之间的重要联系。这是通过一种激素性肠道因子(肠促胰岛素)来实现的,它能增强葡萄糖诱导的胰岛素释放。GIP是研究最深入但并非唯一的肠促胰岛素。此外,GIP似乎对脂质代谢有直接影响。这可以解释为什么脂肪比葡萄糖释放更多的GIP。除了代谢激素胰岛素和胰高血糖素外,胃肠肽的治疗作用尚未得到证实。

相似文献

1
Gastrointestinal peptides--rôle in pathophysiology and disease.胃肠肽——在病理生理学和疾病中的作用
Scand J Gastroenterol Suppl. 1982;77:7-20.
2
GIP, incretin and gastrointestinal disease.胃抑肽、肠促胰岛素与胃肠疾病
Dan Med Bull. 1983 Jun;30(4):205-14.
3
Disturbances of the entero-insular axis.肠-胰岛轴的紊乱。
Scand J Gastroenterol Suppl. 1983;82:111-9.
4
GIP and GLP-1 as incretin hormones: lessons from single and double incretin receptor knockout mice.作为肠促胰岛素激素的葡萄糖依赖性促胰岛素多肽(GIP)和胰高血糖素样肽-1(GLP-1):来自单和双肠促胰岛素受体敲除小鼠的经验教训。
Regul Pept. 2005 Jun 15;128(2):125-34. doi: 10.1016/j.regpep.2004.07.019.
5
Gastric inhibitory polypeptide.胃抑制性多肽
Monogr Endocrinol. 1982;24:III-XI, 1-88.
6
Is glucagon-like peptide 1 an incretin hormone?胰高血糖素样肽-1是一种肠促胰岛素激素吗?
Diabetologia. 1999 Mar;42(3):373-9. doi: 10.1007/s001250051165.
7
Preservation of incretin activity after removal of gastric inhibitory polypeptide (GIP) from rat gut extracts by immunoadsorption.通过免疫吸附从大鼠肠道提取物中去除胃抑制多肽(GIP)后肠促胰岛素活性的保留。
Diabetologia. 1983 Jun;24(6):449-54. doi: 10.1007/BF00257346.
8
Enteroinsular signaling: perspectives on the role of the gastrointestinal hormones glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide in normal and abnormal glucose metabolism.肠胰岛信号传导:关于胃肠激素胰高血糖素样肽1和葡萄糖依赖性促胰岛素多肽在正常和异常葡萄糖代谢中作用的观点
Curr Opin Clin Nutr Metab Care. 2003 Jul;6(4):461-8. doi: 10.1097/01.mco.0000078991.96795.84.
9
New developments in the incretin concept.肠促胰岛素概念的新进展。
Diabetologia. 1985 Aug;28(8):565-73. doi: 10.1007/BF00281990.
10
Clinical endocrinology and metabolism. Glucose-dependent insulinotropic polypeptide/gastric inhibitory polypeptide.临床内分泌学与代谢。葡萄糖依赖性促胰岛素多肽/抑胃多肽。
Best Pract Res Clin Endocrinol Metab. 2004 Dec;18(4):587-606. doi: 10.1016/j.beem.2004.08.007.

引用本文的文献

1
Sample taking problems in measuring actual histamine levels of human gastroduodenal mucosa: specific and general relevance in clinical trials on peptic ulcer pathogenesis and selective proximal vagotomy.测量人胃十二指肠黏膜实际组胺水平时的取样问题:在消化性溃疡发病机制及选择性近端迷走神经切断术临床试验中的特异性和普遍相关性
Gut. 1985 Nov;26(11):1165-78. doi: 10.1136/gut.26.11.1165.
2
Differentiation of gut endoderm in dependence of the notochord.肠道内胚层的分化依赖于脊索。
Anat Embryol (Berl). 1987;176(3):337-43. doi: 10.1007/BF00310188.
3
Increases in intestinal glucose absorption and hepatic glucose uptake elicited by luminal but not vascular glutamine in the jointly perfused small intestine and liver of the rat.
在大鼠联合灌注的小肠和肝脏中,肠腔谷氨酰胺而非血管谷氨酰胺引起肠道葡萄糖吸收增加和肝脏葡萄糖摄取增加。
Biochem J. 1992 May 1;283 ( Pt 3)(Pt 3):759-65. doi: 10.1042/bj2830759.