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肠道在健康和代谢性疾病中的葡萄糖吸收机制及其在食欲调节中的作用。

Mechanisms of Glucose Absorption in the Small Intestine in Health and Metabolic Diseases and Their Role in Appetite Regulation.

机构信息

Pavlov Institute of Physiology, Russian Academy of Sciences, 199034 Saint-Petersburg, Russia.

Neuronal and Neuroendocrine Differentiation and Communication Laboratory, Inserm UMR1239, University of Rouen Normandy, 76130 Mont-Saint-Aignan, France.

出版信息

Nutrients. 2021 Jul 20;13(7):2474. doi: 10.3390/nu13072474.

Abstract

The worldwide prevalence of metabolic diseases such as obesity, metabolic syndrome and type 2 diabetes shows an upward trend in recent decades. A characteristic feature of these diseases is hyperglycemia which can be associated with hyperphagia. Absorption of glucose in the small intestine physiologically contributes to the regulation of blood glucose levels, and hence, appears as a putative target for treatment of hyperglycemia. In fact, recent progress in understanding the molecular and cellular mechanisms of glucose absorption in the gut and its reabsorption in the kidney helped to develop a new strategy of diabetes treatment. Changes in blood glucose levels are also involved in regulation of appetite, suggesting that glucose absorption may be relevant to hyperphagia in metabolic diseases. In this review we discuss the mechanisms of glucose absorption in the small intestine in physiological conditions and their alterations in metabolic diseases as well as their relevance to the regulation of appetite. The key role of SGLT1 transporter in intestinal glucose absorption in both physiological conditions and in diabetes was clearly established. We conclude that although inhibition of small intestinal glucose absorption represents a valuable target for the treatment of hyperglycemia, it is not always suitable for the treatment of hyperphagia. In fact, independent regulation of glucose absorption and appetite requires a more complex approach for the treatment of metabolic diseases.

摘要

近年来,全球范围内肥胖症、代谢综合征和 2 型糖尿病等代谢性疾病的患病率呈上升趋势。这些疾病的一个特征是高血糖,高血糖可能与多食有关。小肠对葡萄糖的吸收在生理上有助于调节血糖水平,因此,它似乎是治疗高血糖的潜在靶点。事实上,近年来对肠道葡萄糖吸收及其在肾脏中的重吸收的分子和细胞机制的理解进展,有助于开发治疗糖尿病的新策略。血糖水平的变化也参与了食欲的调节,这表明葡萄糖吸收可能与代谢性疾病中的多食有关。在这篇综述中,我们讨论了在生理条件下小肠葡萄糖吸收的机制及其在代谢性疾病中的变化,以及它们与食欲调节的相关性。SGLT1 转运体在小肠葡萄糖吸收中的关键作用在生理条件和糖尿病中都得到了明确的证实。我们的结论是,尽管抑制小肠葡萄糖吸收是治疗高血糖的一个有价值的靶点,但它并不总是适合治疗多食。事实上,要治疗代谢性疾病,需要更复杂的方法来独立调节葡萄糖吸收和食欲。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc7/8308647/30374cc3ae1c/nutrients-13-02474-g001.jpg

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