Targeting the programmed cell death (PCD) signaling mechanism with natural substances for the treatment of diabetic cardiomyopathy (DCM)

被引:5
作者
Xuan, Xiaoyu [1 ]
Zhang, Shiliang [2 ]
机构
[1] Shandong Univ Tradit Chinese Med, Sch Clin Med 1, Jinan, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Dept Cardiol, Affiliated Hosp, Jinan, Peoples R China
关键词
diabetic cardiomyopathy; natural substances; programmed cell death; signaling pathways; therapy; MITOCHONDRIAL DYNAMICS; INDUCED APOPTOSIS; OXIDATIVE STRESS; AUTOPHAGY; PYROPTOSIS; ADIPONECTIN; METFORMIN; PROTECTS; MELLITUS; COMPLEX;
D O I
10.1002/ptr.7992
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diabetic cardiomyopathy (DCM) is one of the severe complications of diabetes, characterized by structural and functional abnormalities in the hearts of diabetic patients without hypertension, coronary heart disease, or valvular heart disease. DCM can progress to heart failure, which is a significant cause of death in diabetic patients, but currently, there is no effective treatment available. Programmed cell death (PCD) is a genetically regulated form of cell death that includes apoptosis, autophagy, necroptosis, ferroptosis, and pyroptosis. PCD is essential for tissue homeostasis and normal development of the body. DCM is a complex condition, and abnormalities in the cascade of PCD signaling have been observed in its pathological process, suggesting that targeting PCD could be a potential therapeutic strategy. Studies have shown that natural substances can effectively modulate PCD to intervene in the treatment of DCM, and their use is safe. This review explores the role of different forms of PCD in the pathogenesis of DCM and summarizes the research progress in targeting PCD with natural substances to treat DCM. It can serve as a basis for further research and drug development to provide new treatment strategies for DCM patients.
引用
收藏
页码:5495 / 5508
页数:14
相关论文
共 95 条
[51]   Ginsenoside-Rb1 Improved Diabetic Cardiomyopathy through Regulating Calcium Signaling by Alleviating Protein O-GlcNAcylation [J].
Qin, Linhui ;
Wang, Jianping ;
Zhao, RongRong ;
Zhang, Xiao ;
Mei, Yingwu .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2019, 67 (51) :14074-14085
[52]   Ginsenoside Rg1 ameliorates cardiac oxidative stress and inflammation in streptozotocin-induced diabetic rats [J].
Qin, Qiaoji ;
Lin, Nan ;
Huang, Huan ;
Zhang, Xuezhi ;
Cao, Xuelei ;
Wang, Yongbin ;
Li, Peng .
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY, 2019, 12 :1091-1103
[53]  
Rao S., 2022, J NANOBIOTECHNOL, V20, P1
[54]   Curcumin alleviates oxidative stress and inhibits apoptosis in diabetic cardiomyopathy via Sirt1-Foxo1 and PI3K-Akt signalling pathways [J].
Ren, Bin-cheng ;
Zhang, Yu-fei ;
Liu, Shan-shan ;
Cheng, Xiao-jing ;
Yang, Xin ;
Cui, Xiao-guang ;
Zhao, Xin-rui ;
Zhao, Hui ;
Hao, Min-feng ;
Li, Meng-dan ;
Tie, Yuan-yuan ;
Qu, Li ;
Li, Xue-yi .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2020, 24 (21) :12355-12367
[55]   Basic Mechanisms of Diabetic Heart Disease [J].
Ritchie, Rebecca H. ;
Abel, E. Dale .
CIRCULATION RESEARCH, 2020, 126 (11) :1501-1525
[56]  
SAEEDI P, 2019, DIABETES RES CLIN PR, V157, DOI [DOI 10.1016/J.DIABRES.2019.107843, 10.1016/j.diabres.2019, DOI 10.1016/J.DIABRES.2019]
[57]   Mechanism of Ferroptosis and Its Role in Type 2 Diabetes Mellitus [J].
Sha, Wenxin ;
Hu, Fei ;
Xi, Yang ;
Chu, Yudong ;
Bu, Shizhong .
JOURNAL OF DIABETES RESEARCH, 2021, 2021
[58]  
Sharma A., 2013, Journal of Pharmacognosy and Phytochemistry, V1, P108
[59]  
Sharma AK., 2013, INT J TOXICOLOGICAL, V5, P15
[60]   Gemfibrozil and its combination with metformin on pleiotropic effect on IL-10 and adiponectin and anti-atherogenic treatment in insulin resistant type 2 diabetes mellitus rats [J].
Sharma, Ashish Kumar ;
Raikwar, Sachin Kumar ;
Kurmi, Muneem Kumar ;
Srinivasan, Bharthu Parthsarthi .
INFLAMMOPHARMACOLOGY, 2013, 21 (02) :137-145