Neuroprotective Effect of Sitagliptin beyond the Incretin Effect: A Narrative Review.

Ali Mohammad Pourbagher-Shahri, Fatemeh Forouzanfar
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Abstract

Sitagliptin is a dipeptidyl peptidase-IV inhibitor approved for treating type 2 diabetes mellitus. It increases the active form of incretin Glucagon-like Peptide-1 (GLP-1). The GLP-1 peptide prevents damage to neurons due to its anti-inflammatory and anti-apoptotic activities. This article summarizes the studies assessing the neuroprotective properties of sitagliptin, especially through the GLP-1 pathway. The outcomes of experimental research indicate that sitagliptin has a decreasing effect on inflammation response. Sitagliptin decreases proinflammatory factors, such as Glial Fibrillary Acidic Protein (GFAP), Nuclear factor kappa B (NF-κB), Tumor Necrosis Factor-α (TNF- α), and Interleukin-6 (IL-6). It also decreases glutamate levels, the primary excitatory neurotransmitter. Furthermore, sitagliptin shows antioxidative and antiapoptotic effects. Lastly, sitagliptin may provide a novel agent for the management of neurological disease.

西格列汀在肠促胰岛素作用之外的神经保护作用:叙述性综述。
西格列汀是一种被批准用于治疗2型糖尿病的二肽基肽酶- iv抑制剂。它增加了胰高血糖素样肽-1 (GLP-1)的活性形式。GLP-1肽通过其抗炎和抗凋亡活性防止神经元损伤。本文综述了西格列汀神经保护作用的研究进展,特别是通过GLP-1通路。实验研究结果表明西格列汀对炎症反应有降低作用。西格列汀降低促炎因子,如胶质纤维酸性蛋白(GFAP)、核因子κB (NF-κB)、肿瘤坏死因子-α (TNF- α)、白细胞介素-6 (IL-6)。它还会降低主要兴奋性神经递质谷氨酸水平。此外,西格列汀显示抗氧化和抗凋亡作用。最后,西格列汀可能为神经系统疾病的治疗提供一种新的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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