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口腔葡萄糖转运蛋白的糖信号会引发小鼠的头相胰岛素释放。

Sugar signals from oral glucose transporters elicit cephalic-phase insulin release in mice.

机构信息

Department of Oral Physiology, Graduate School of Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, 700-8525, Japan.

Department of Dental Anesthesiology and Special Care Dentistry, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

出版信息

J Physiol Sci. 2023 Jul 31;73(1):16. doi: 10.1186/s12576-023-00875-3.

Abstract

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.

摘要

头相胰岛素释放(CPIR)发生在餐后血糖升高之前。尽管葡萄糖是最有可能引发 CPIR 的线索,但涉及的外周感觉系统尚未完全阐明。因此,我们研究了 T1R3 依赖性味觉受体的甜味感知和口腔葡萄糖转运蛋白的糖感知在诱导 CPIR 中的作用。在野生型(C57BL/6)和 T1R3 敲除小鼠中,自发口服葡萄糖可显著增加 5 分钟后的血浆胰岛素,而胃内输注则不能。口服葡萄糖转运蛋白抑制剂根皮苷和根皮素可显著减少自发口服后 CPIR。此外,与 WT 小鼠自发口服葡萄糖相比,WT 小鼠自发口服非代谢性葡萄糖类似物后血浆胰岛素的快速增加明显较小。综上所述,T1R3 依赖性受体不是 CPIR 所必需的,但口腔葡萄糖转运蛋白对糖诱导 CPIR 有很大贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b02/10717186/52b13e8cc751/12576_2023_875_Fig1_HTML.jpg

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