Dunaliella salina Alga Protects against Myocardial Ischemia/Reperfusion Injury by Attenuating TLR4 Signaling.
Chin-Feng TsaiHui-Wen LinJiuan-Miaw LiaoKe-Min ChenJen-Wei TsaiChia-Sung ChangChia-Yu ChouHsing-Hui SuPei-Hsun LiuYa-Chun ChuYi-Hsin WangMeilin WangShiang-Suo HuangPublished in: International journal of molecular sciences (2023)
Myocardial ischemia/reperfusion (I/R) injury is marked by rapid increase in inflammation and not only results in myocardial apoptosis but also compromises the myocardial function. Dunaliella salina ( D. salina ), a halophilic unicellular microalga, has been used as a provitamin A carotenoid supplement and color additive. Several studies have reported that D. salina extract could attenuate lipopolysaccharides-induced inflammatory effects and regulate the virus-induced inflammatory response in macrophages. However, the effects of D. salina on myocardial I/R injury remain unknown. Therefore, we aimed to investigate the cardioprotection of D. salina extract in rats subjected to myocardial I/R injury that was induced by occlusion of the left anterior descending coronary artery for 1 h followed by 3 h of reperfusion. Compared with the vehicle group, the myocardial infarct size significantly decreased in rats that were pre-treated with D. salina . D. salina significantly attenuated the expressions of TLR4, COX-2 and the activity of STAT1, JAK2, IκB, NF-κB. Furthermore, D. salina significantly inhibited the activation of caspase-3 and the levels of Beclin-1, p62, LC3-I/II. This study is the first to report that the cardioprotective effects of D. salina may mediate anti-inflammatory and anti-apoptotic activities and decrease autophagy through the TLR4-mediated signaling pathway to antagonize myocardial I/R injury.
Keyphrases
- left ventricular
- inflammatory response
- oxidative stress
- signaling pathway
- anti inflammatory
- coronary artery
- cell death
- toll like receptor
- acute myocardial infarction
- diabetic rats
- lipopolysaccharide induced
- high glucose
- pi k akt
- induced apoptosis
- drug induced
- pulmonary artery
- acute coronary syndrome
- epithelial mesenchymal transition
- cell proliferation
- percutaneous coronary intervention