来自口服葡萄糖转运体的糖信号可引起小鼠头相胰岛素释放。

IF 2.6 4区 医学 Q2 PHYSIOLOGY
Mitsuhito Takamori, Yoshihiro Mitoh, Kengo Horie, Masahiko Egusa, Takuya Miyawaki, Ryusuke Yoshida
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引用次数: 0

摘要

头相胰岛素释放(CPIR)发生在餐后血糖升高之前。虽然葡萄糖是诱导 CPIR 的最合理线索,但所涉及的外周感觉系统尚未完全阐明。因此,我们研究了依赖 T1R3 的味觉受体对甜味的感知和口咽部葡萄糖转运体对糖的感知在诱导 CPIR 中的作用。野生型小鼠(C57BL/6)和 T1R3 基因敲除小鼠自发口服葡萄糖 5 分钟后血浆胰岛素明显升高,而胃内输注葡萄糖则没有升高。自发口服葡萄糖转运体抑制剂phlorizin和phloretin可显著降低CPIR。此外,WT 小鼠自发口服不可代谢的葡萄糖类似物后,血浆胰岛素的快速增加明显小于自发口服葡萄糖的 WT 小鼠。综上所述,CPIR 不需要 T1R3 依赖性受体,但口服葡萄糖转运体对糖类诱导 CPIR 有很大贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sugar signals from oral glucose transporters elicit cephalic-phase insulin release in mice.

Cephalic-phase insulin release (CPIR) occurs before blood glucose increases after a meal. Although glucose is the most plausible cue to induce CPIR, peripheral sensory systems involved are not fully elucidated. We therefore examined roles of sweet sensing by a T1R3-dependent taste receptor and sugar sensing by oral glucose transporters in the oropharyngeal region in inducing CPIR. Spontaneous oral ingestion of glucose significantly increased plasma insulin 5 min later in wild-type (C57BL/6) and T1R3-knockout mice, but intragastric infusion did not. Oral treatment of glucose transporter inhibitors phlorizin and phloretin significantly reduced CPIR after spontaneous oral ingestion. In addition, a rapid increase in plasma insulin was significantly smaller in WT mice with spontaneous oral ingestion of nonmetabolizable glucose analog than in WT mice with spontaneous oral ingestion of glucose. Taken together, the T1R3-dependent receptor is not required for CPIR, but oral glucose transporters greatly contribute to induction of CPIR by sugars.

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来源期刊
CiteScore
4.40
自引率
4.30%
发文量
27
审稿时长
6-12 weeks
期刊介绍: The Journal of Physiological Sciences publishes peer-reviewed original papers, reviews, short communications, technical notes, and letters to the editor, based on the principles and theories of modern physiology and addressed to the international scientific community. All fields of physiology are covered, encompassing molecular, cellular and systems physiology. The emphasis is on human and vertebrate physiology, but comparative papers are also considered. The process of obtaining results must be ethically sound. Fields covered: Adaptation and environment Autonomic nervous function Biophysics Cell sensors and signaling Central nervous system and brain sciences Endocrinology and metabolism Excitable membranes and neural cell physiology Exercise physiology Gastrointestinal and kidney physiology Heart and circulatory physiology Molecular and cellular physiology Muscle physiology Physiome/systems biology Respiration physiology Senses.
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