肠道胰高血糖素样肽-1 在 1 型糖尿病管理中的降糖反调节作用。

IF 4.2 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Ke-Xin Zhang, Cheng-Xia Kan, Yu-Qun Wang, Ning-Ning Hou, Xiao-Dong Sun
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引用次数: 0

摘要

1型糖尿病(T1D)的特点是自身免疫破坏胰腺β细胞,导致绝对胰岛素缺乏和需要外源性胰岛素。T1D治疗的一个重要问题是低血糖,它会因反调节机制受损而恶化。有效的反调节包括胰高血糖素和肾上腺素等激素,它们的作用是恢复正常的血糖水平。然而,在T1D中,这些机制经常失效,特别是在反复低血糖后,导致低血糖相关的自主神经衰竭。最近的研究表明,肠道胰高血糖素样肽-1 (GLP-1)水平升高通过减少胰高血糖素和肾上腺素的分泌而损害反调节反应。这篇社论强调了GLP-1在促肠促胰岛素作用之外的作用,有助于降低血糖的反调节。这种理解需要对基于glp -1的T1D治疗采取细致入微的方法,平衡血糖控制的益处与潜在风险。未来的研究应该深入研究GLP-1作用的机制,并探索潜在的干预措施来改善低血糖对抗调节。目标是提高T1D患者的安全性和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intestinal glucagon-like peptide-1 in hypoglycemic counterregulation for type 1 diabetes management.

Type 1 diabetes (T1D) is characterized by the autoimmune destruction of pancreatic beta cells, leading to absolute insulin deficiency and the need for exogenous insulin. A significant concern in T1D management is hypoglycemia, which is worsened by impaired counterregulatory mechanisms. Effective counterregulation involves hormones such as glucagon and adrenaline, which work to restore normal blood glucose levels. However, in T1D, these mechanisms often fail, particularly after recurrent hypoglycemia, resulting in hypoglycemia-associated autonomic failure. Recent research indicates that elevated levels of intestinal glucagon-like peptide-1 (GLP-1) impair counterregulatory responses by reducing the secretion of glucagon and adrenaline. This editorial underscores GLP-1's role beyond its incretin effects, contributing to impaired hypoglycemic counterregulation. This understanding necessitates a nuanced approach to GLP-1-based therapies in T1D, balancing the benefits of glycemic control with potential risks. Future research should delve into the mechanisms behind GLP-1's effects and explore potential interventions to improve hypoglycemic counterregulation. The goal is to enhance the safety and quality of life for T1D patients.

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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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