Center of Systems Biology, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece.
Institute for Molecular Cardiovascular Research, RWTH Aachen University Hospital, 52074 Aachen, Germany.
Int J Mol Sci. 2023 Aug 31;24(17):13540. doi: 10.3390/ijms241713540.
Type II diabetes mellitus (T2DM) accounts for approximately 90% of all diabetes mellitus cases in the world. Glucagon-like peptide-1 receptor (GLP-1R) agonists have established an increased capability to target directly or indirectly six core defects associated with T2DM, while the underlying molecular mechanisms of these pharmacological effects are not fully known. This exploratory study was conducted to analyze the effect of treatment with GLP-1R agonists on the urinary peptidome of T2DM patients. Urine samples of thirty-two T2DM patients from the PROVALID study ("A Prospective Cohort Study in Patients with T2DM for Validation of Biomarkers") collected pre- and post-treatment with GLP-1R agonist drugs were analyzed by CE-MS. In total, 70 urinary peptides were significantly affected by GLP-1R agonist treatment, generated from 26 different proteins. The downregulation of MMP proteases, based on the concordant downregulation of urinary collagen peptides, was highlighted. Treatment also resulted in the downregulation of peptides from , , , , , , , , , , and , many of which were previously found to be associated with increased insulin resistance and inflammation. The findings indicate potential molecular mechanisms of GLP-1R agonists in the context of the management of T2DM and the prevention or delaying of the progression of its associated diseases.
2 型糖尿病(T2DM)约占全球所有糖尿病病例的 90%。胰高血糖素样肽-1 受体(GLP-1R)激动剂已被证明具有增强的能力,可以直接或间接地针对与 T2DM 相关的六个核心缺陷,而这些药理作用的潜在分子机制尚不完全清楚。这项探索性研究旨在分析 GLP-1R 激动剂治疗对 T2DM 患者尿肽组的影响。对来自 PROVALID 研究(“用于验证生物标志物的 T2DM 患者的前瞻性队列研究”)的 32 名 T2DM 患者的尿液样本进行了分析,这些样本在接受 GLP-1R 激动剂药物治疗前后均进行了 CE-MS 分析。总共,70 种尿肽受 GLP-1R 激动剂治疗的影响,这些肽来源于 26 种不同的蛋白质。基于尿胶原肽的一致下调,MMP 蛋白酶的下调尤为明显。治疗还导致来自 、 、 、 、 、 、 、 、 和 的肽下调,其中许多肽先前与胰岛素抵抗和炎症增加有关。这些发现表明 GLP-1R 激动剂在 T2DM 管理以及预防或延缓其相关疾病进展方面的潜在分子机制。