Cell signaling and biological pathway in cardiovascular diseases.
Cheong-Whan ChaeYoo-Wook KwonPublished in: Archives of pharmacal research (2019)
Currently, coronary artery disease accounts for a large proportion of deaths occurring worldwide. Damage to the heart muscle over a short period of time leads to myocardial infarction (MI). The biological mechanisms of atherosclerosis, one of the causes of MI, have been well studied. Resistin, a type of adipokine, is closely associated with intravascular level of low-density lipoprotein cholesterol and augmentation of the expression of adhesion molecules in endothelial cells. Therefore, resistin, which is highly associated with inflammation, can progress into coronary artery disease. Adenylyl cyclase associated protein 1, a binding partner of resistin, also plays an important role in inducing pro-inflammatory cytokines. The induction of these cytokines can aggravate atherosclerosis by promoting severe plaque rupture of the lesion site. Recently, drugs, such as statins that can inhibit inflammation have been extensively studied. The development of effective new drugs that can directly or indirectly block pro-inflammatory cytokines may have a great potential in the treatment of coronary artery disease in the future.
Keyphrases
- coronary artery disease
- cardiovascular disease
- oxidative stress
- percutaneous coronary intervention
- cardiovascular events
- endothelial cells
- coronary artery bypass grafting
- heart failure
- poor prognosis
- anti inflammatory
- single cell
- cell therapy
- skeletal muscle
- multidrug resistant
- cardiovascular risk factors
- drug induced
- coronary artery
- stem cells
- escherichia coli
- biofilm formation
- human immunodeficiency virus
- current status
- climate change
- soft tissue
- pseudomonas aeruginosa
- mesenchymal stem cells
- hepatitis c virus
- acute coronary syndrome
- replacement therapy
- high glucose