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利拉鲁肽预防性治疗可预防沃尔弗拉姆综合征大鼠模型葡萄糖不耐受的发展。

Preventive treatment with liraglutide protects against development of glucose intolerance in a rat model of Wolfram syndrome.

机构信息

Institute of Biomedicine and Translational Medicine, Laboratory Animal Centre, University of Tartu, 14B Ravila Street, Tartu, 50411, Estonia.

Institute of Biomedicine and Translational Medicine, Department of Physiology, University of Tartu, 19 Ravila Street, Tartu, 50411, Estonia.

出版信息

Sci Rep. 2018 Jul 5;8(1):10183. doi: 10.1038/s41598-018-28314-z.

Abstract

Wolfram syndrome (WS) is a rare autosomal recessive disorder caused by mutations in the WFS1 (Wolframin1) gene. The syndrome first manifests as diabetes mellitus, followed by optic nerve atrophy, deafness, and neurodegeneration. The underlying mechanism is believed to be a dysregulation of endoplasmic reticulum (ER) stress response, which ultimately leads to cellular death. Treatment with glucagon-like peptide-1 (GLP-1) receptor agonists has been shown to normalize ER stress response in several in vitro and in vivo models. Early chronic intervention with the GLP-1 receptor agonist liraglutide starting before the onset of metabolic symptoms prevented the development of glucose intolerance, improved insulin and glucagon secretion control, reduced ER stress and inflammation in Langerhans islets in Wfs1 mutant rats. Thus, treatment with GLP-1 receptor agonists might be a promising strategy as a preventive treatment for human WS patients.

摘要

沃尔弗拉姆综合征(WS)是一种罕见的常染色体隐性遗传病,由 WFS1(沃尔弗拉明 1 基因)基因突变引起。该综合征首先表现为糖尿病,随后出现视神经萎缩、耳聋和神经退行性变。其潜在机制被认为是内质网(ER)应激反应失调,最终导致细胞死亡。胰高血糖素样肽-1(GLP-1)受体激动剂的治疗已被证明可在几种体外和体内模型中使 ER 应激反应正常化。在代谢症状出现之前,即开始用 GLP-1 受体激动剂利拉鲁肽进行早期慢性干预,可以预防葡萄糖不耐受的发生,改善胰岛素和胰高血糖素分泌控制,减少 Wfs1 突变大鼠胰岛中的 ER 应激和炎症。因此,GLP-1 受体激动剂的治疗可能是一种有前途的策略,作为人类 WS 患者的预防治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6dc/6033861/78a5ff3c9849/41598_2018_28314_Fig1_HTML.jpg

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