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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Dose rectification of an imbalance between DPP DPP 4 and GLP GLP ‐1 ameliorates chronic stress‐related vascular aging and atherosclerosis?
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Dose rectification of an imbalance between DPP DPP 4 and GLP GLP ‐1 ameliorates chronic stress‐related vascular aging and atherosclerosis?

机译:DPP DPP 4和GLP GLP -1之间不平衡的剂量矫正改善慢性应激相关的血管老化和动脉粥样硬化?

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摘要

Summary Exposure to psychosocial stress is a risk factor for cardiovascular disease, including vascular aging and regeneration. Dipeptidyl peptidase‐4 ( DPP ‐4) exerts many physiological and pharmacological functions by regulating its extremely abundant substrates [eg., glucagon‐like peptide‐1 ( GLP ‐1), stromal cell‐derived factor‐1α/C‐X‐C chemokine receptor type‐4, etc.]. Over the past decade, emerging data has revealed unexpected roles for DPP ‐4 and GLP ‐1 in intracellular signaling, oxidative stress production, lipid metabolism, cell apoptosis, immune activation, insulin resistance, and inflammation. This mini review focuses on recent findings in this field, highlighting an imbalance between DPP 4 and GLP ‐1 as a potential therapeutic target in the management of vascular aging and atherosclerosis in animals under experimental stress conditions.
机译:发明内容暴露于心理社会应激是心血管疾病的危险因素,包括血管衰老和再生。 二肽基肽酶-4(DPP -4)通过调节其极丰的底物[例如,胰高血糖素肽-1(GLP-1),基质细胞衍生因子-1α/ C-X-C来施加许多生理和药理功能 趋化因子受体类型-4等。 在过去十年中,新兴数据揭示了DPP -4和GLP -1在细胞内信号,氧化应激生产,脂质代谢,细胞凋亡,免疫激活,胰岛素抵抗和炎症中的意外角色。 此迷你评论重点介绍该领域的最近调查结果,突出了DPP 4和GLP -1之间的不平衡,作为在实验应激条件下管理血管老化和动脉粥样硬化的潜在治疗目标。

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