Yixin-Shu Capsules Ameliorated Ischemia-Induced Heart Failure by Restoring Trx2 and Inhibiting JNK/p38 Activation.
Changpei XiangFangbo ZhangJinhuan GaoFeifei GuoMao ZhangRui ZhouJunying WeiPing WangYi ZhangJingjing ZhangHongjun YangPublished in: Oxidative medicine and cellular longevity (2021)
Traditional Chinese medicine has shown great safety and efficacy in the treatment of heart failure (HF), whereas the mechanism remains unclear. In this study, the protective effect of Yixin-shu (YXS) capsules, a conventional medicine for various cardiovascular diseases, against myocardial ischemia-induced HF in rats was systematically investigated by RNA-seq technology. HF rats treated with YXS (0.8 or 1.6 g/kg/d, ig) for 6 weeks had significantly decreased brain natriuretic peptide (BNP) and atrial natriuretic peptide (ANP) and collagen III and attenuated cardiac structure rupture and collagen deposition. Additionally, YXS treatment decreased the levels of interleukin-1β (IL-1β), interleukin 6 (IL-6), tumor necrosis factor-α (TNF-α), and lactate dehydrogenase (LDH) and TUNEL-positive rate and the nitrotyrosine staining, but increased levels of glutathione (GSH), total antioxidant capacity (T-AOC) activity, and mitochondrial membrane potential. Further experiments demonstrated that YXS restored Trx2 and inhibited the phosphorylation of JNK and p38, thereby improving cardiac function in the rats with HF. Silencing Trx2 decreased the protection of YXS in the response to H2O2 as evidenced by the increase of caspase-3 activity and decrease of GSH level. Thus, YXS enhanced heart function and decreased myocardial damage through restoring Trx2 and inhibiting JNK and p38 activation in ischemia-induced HF.
Keyphrases
- heart failure
- acute heart failure
- signaling pathway
- left ventricular
- rna seq
- cell death
- high glucose
- diabetic rats
- oxidative stress
- rheumatoid arthritis
- induced apoptosis
- cardiovascular disease
- atrial fibrillation
- single cell
- drug induced
- cardiac resynchronization therapy
- endothelial cells
- mass spectrometry
- risk assessment
- coronary artery disease
- protein kinase