New insights into oxidative stress and inflammation during diabetes mellitus-accelerated atherosclerosis

被引:511
作者
Yuan, Ting [1 ]
Yang, Ting [1 ]
Chen, Huan [1 ]
Fu, Danli [1 ]
Hu, Yangyang [1 ]
Wang, Jing [1 ]
Yuan, Qing [1 ]
Yu, Hong [1 ]
Xu, Wenfeng [1 ]
Xie, Xiang [1 ]
机构
[1] Southwest Med Univ, Sch Basic Med Sci, Luzhou 646000, Sichuan, Peoples R China
关键词
Atherosclerosis; Diabetes mellitus; Reactive oxygen species; Gut microbiota; MicroRNA; ACTIVATED PROTEIN-KINASE; ENDOPLASMIC-RETICULUM STRESS; SMOOTH-MUSCLE-CELLS; UBIQUITIN-PROTEASOME SYSTEM; ALDOSE REDUCTASE EXPRESSION; C/EBP HOMOLOGOUS PROTEIN; GLYCATION END-PRODUCTS; KAPPA-B-ALPHA; NITRIC-OXIDE; INSULIN-RESISTANCE;
D O I
10.1016/j.redox.2018.09.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxidative stress and inflammation interact in the development of diabetic atherosclerosis. Intracellular hyperglycemia promotes production of mitochondrial reactive oxygen species (ROS), increased formation of intracellular advanced glycation end-products, activation of protein kinase C, and increased polyol pathway flux. ROS directly increase the expression of inflammatory and adhesion factors, formation of oxidized-low density lipoprotein, and insulin resistance. They activate the ubiquitin pathway, inhibit the activation of AMP-protein kinase and adiponectin, decrease endothelial nitric oxide synthase activity, all of which accelerate atherosclerosis. Changes in the composition of the gut microbiota and changes in microRNA expression that influence the regulation of target genes that occur in diabetes interact with increased ROS and inflammation to promote atherosclerosis. This review highlights the consequences of the sustained increase of ROS production and inflammation that influence the acceleration of atherosclerosis by diabetes. The potential contributions of changes in the gut microbiota and microRNA expression are discussed.
引用
收藏
页码:247 / 260
页数:14
相关论文
共 220 条
[11]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[12]   (Dis)Trust your gut: the gut microbiome in age-related inflammation, health, and disease [J].
Buford, Thomas W. .
MICROBIOME, 2017, 5 :1-11
[13]   Obesity, diabetes mellitus, atherosclerosis and chronic periodontitis: a shared pathology via oxidative stress and mitochondrial dysfunction? [J].
Bullon, Pedro ;
Newman, Hubert N. ;
Battino, Maurizio .
PERIODONTOLOGY 2000, 2014, 64 (01) :139-153
[14]   Advanced glycation end-products produced systemically and by macrophages: A common contributor to inflammation and degenerative diseases [J].
Byun, Kyunghee ;
Yoo, YongCheol ;
Son, Myeongjoo ;
Lee, Jaesuk ;
Jeong, Goo-Bo ;
Park, Young Mok ;
Salekdeh, Ghasem Hosseini ;
Lee, Bonghee .
PHARMACOLOGY & THERAPEUTICS, 2017, 177 :44-55
[15]   Myeloid Deletion of α1AMPK Exacerbates Atherosclerosis in LDL Receptor Knockout (LDLRKO) Mice [J].
Cao, Qiang ;
Cui, Xin ;
Wu, Rui ;
Zha, Lin ;
Wang, Xianfeng ;
Parks, John S. ;
Yu, Liqing ;
Shi, Hang ;
Xue, Bingzhong .
DIABETES, 2016, 65 (06) :1565-1576
[16]   Decreased production of neuronal NOS-derived hydrogen peroxide contributes to endothelial dysfunction in atherosclerosis [J].
Capettini, L. S. A. ;
Cortes, S. F. ;
Silva, J. F. ;
Alvarez-Leite, J. I. ;
Lemos, V. S. .
BRITISH JOURNAL OF PHARMACOLOGY, 2011, 164 (06) :1738-1748
[17]   Adiponectin Blocks Interleukin-18-mediated Endothelial Cell Death via APPL1-dependent AMP-activated Protein Kinase (AMPK) Activation and IKK/NF-κB/PTEN Suppression [J].
Chandrasekar, Bysani ;
Boylston, William H. ;
Venkatachalam, Kaliyamurthi ;
Webster, Nicholas J. G. ;
Prabhu, Sumanth D. ;
Valente, Anthony J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (36) :24889-24898
[18]   Kinase-SUMO networks in diabetes-mediated cardiovascular disease [J].
Chang, Eugene ;
Abe, Jun-ichi .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2016, 65 (05) :623-633
[19]   Identification of Signaling Pathways Involved in Aberrant Production of Adipokines in Adipocytes Undergoing Oxidative Stress [J].
Chen, Baoying ;
Wei, Jingguo ;
Wang, Wei ;
Cui, Guangbin ;
Zhao, Yufeng ;
Zhu, Xiaoxing ;
Zhu, Miaozhang ;
Guo, Wei ;
Yu, Jun .
ARCHIVES OF MEDICAL RESEARCH, 2009, 40 (04) :241-248
[20]   AMP-activated protein kinase attenuates oxLDL uptake in macrophages through PP2A/NF-κB/LOX-1 pathway [J].
Chen, Bo ;
Li, Jin ;
Zhu, Haibo .
VASCULAR PHARMACOLOGY, 2016, 85 :1-10