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胃肠道中的氨基酸感知

Amino acid sensing in the gastrointestinal tract.

作者信息

San Gabriel Ana, Uneyama Hisayuki

机构信息

Scientific Affairs, Communications Department, Ajinomoto Co., Inc., Tokyo, 104-8315, Japan.

出版信息

Amino Acids. 2013 Sep;45(3):451-61. doi: 10.1007/s00726-012-1371-2. Epub 2012 Aug 3.

Abstract

Rapid progress in gastroenterology during the first part of the last century has shown that gastrointestinal (GI) function is regulated by neuroendocrine, paracrine and endocrine signals. However, recent advances in chemical sensing, especially in the last decade, have revealed that free L-amino acids (AA), among other nutrients, play a critical role in modifying exocrine and endocrine secretion, modulating protein digestion, metabolism and nutrient utilization, and supporting the integrity and defense of the GI mucosa. Many of the mechanisms by which AAs elicit these functions in the GI has been linked to the traditional concept of hormone release and nervous system activation. But most these effects are not direct. AAs appear to function by binding to a chemical communication system such as G protein-coupled receptors (GPCRs) that activate signaling pathways. These intracellular signals, although their molecular bases are not completely elucidated yet, are the ones responsible for the neuronal activity and release of hormones that in turn regulate GI functions. This review aims to describe the distribution of the known GPCRs from the class 3 superfamily that bind to different kinds of AA, especially from the oropharyngeal cavity to the stomach, what kind of taste qualities they elicit, such as umami, bitter or sweet, and their activity in the GI tract.

摘要

上世纪上半叶胃肠病学的快速发展表明,胃肠(GI)功能受神经内分泌、旁分泌和内分泌信号调节。然而,化学传感领域的最新进展,尤其是过去十年的进展,揭示了游离L-氨基酸(AA)以及其他营养素在调节外分泌和内分泌分泌、调节蛋白质消化、代谢和营养利用,以及维持GI黏膜的完整性和防御功能方面发挥着关键作用。AA在胃肠道发挥这些功能的许多机制与激素释放和神经系统激活的传统概念有关。但这些作用大多不是直接的。AA似乎通过与化学通讯系统(如激活信号通路的G蛋白偶联受体(GPCRs))结合来发挥作用。这些细胞内信号,尽管其分子基础尚未完全阐明,但却是负责神经元活动和激素释放的信号,进而调节GI功能。本综述旨在描述3类超家族中已知的与不同种类AA结合的GPCRs的分布,特别是从口咽腔到胃的分布,它们引发的味觉特性,如鲜味、苦味或甜味,以及它们在胃肠道中的活性。

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