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NF NF ‐κB as the mediator of metformin's effect on ageing and ageing‐related diseases

机译:NF NF-κB作为二甲双胍对衰老和衰老相关疾病的影响的介质

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Summary Ageing can be defined as the progressive failure of repair and maintenance systems with a consequent accumulation of cellular damage in nucleic acids, proteins, and lipids. These various types of damage promote ageing by driving cellular senescence and apoptosis. The nuclear factor‐kappa B ( NF ‐ kB ) pathway is one of the key mediators of ageing and this pathway is activated by genotoxic, oxidative and inflammatory stress, and regulates expression of cytokines, growth factors, and genes that regulate apoptosis, cell‐cycle progression, and inflammation. Therefore, NF ‐ kB is increased in a variety of tissues with ageing, thus the inhibition of NF ‐ kB leads to delayed onset of ageing‐related symptoms and pathologies such as diabetes, atherosclerosis, and cancer. Metformin is often used as an anti‐diabetic medication in type 2 diabetes throughout the world and appears to be a potential anti‐ageing agent. Owing to its antioxidant, anticancer, cardio‐protective and anti‐inflammatory properties, metformin has become a potential candidate drug, improving in the context of ageing and ageing‐related diseases. An inappropriate NF ‐ kB activation is associated with diseases and pathologic conditions which can impair the activity of genes involved in cell senescence, apoptosis, immunity, and inflammation. Metformin, inhibiting the expression of NF ‐ kB gene, eliminates the susceptibility to common diseases. This review underlines the pleiotropic effects of metformin in ageing and different ageing‐related diseases and attributes its effects to the modulation of NF‐ kB .
机译:总结老化可以定义为维修和维护系统的逐步失败,随后核酸,蛋白质和脂质的细胞损伤积累。这些各种类型的损害通过驱动细胞衰老和细胞凋亡来促进老化。核因子-Kappa B(NF - KB)途径是老化的关键介质之一,并且通过遗传毒性,氧化和炎症应激激活该途径,并调节细胞因子,生长因子和调节细胞凋亡的基因的表达,循环进展和炎症。因此,NF - KB在具有老化的各种组织中增加,因此NF - Kb的抑制导致延迟衰老相关症状和病理,例如糖尿病,动脉粥样硬化和癌症。二甲双胍通常用作全世界2型糖尿病中的抗糖尿病药物,似乎是潜在的抗衰老剂。由于其抗氧化剂,抗癌,心脏保护和抗炎特性,二甲双胍已成为潜在的候选药物,在衰老和衰老相关疾病的背景下改善。不合适的NF - KB活化与疾病和病理条件有关,可以损害涉及细胞衰老,细胞凋亡,免疫和炎症的基因的活动。抑制NF - KB基因表达的二甲双胍消除了对常见疾病的敏感性。本综述强调了二甲双胍在老化和不同衰老相关疾病中的脂肪效应,并将其作用归因于NF-KB的调节。

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