Literature DB >> 28627591

Chinese herbal medicine Xinji pill protects the heart from ischemia/reperfusion injury through the Akt/Nrf2 pathway.

Qiuzhen Yuan1, Ruiming Chen2, Xu Zheng3, Maixia Meng2, Yuping Kao1, Junfeng Liu1, Xuefeng Gan1, Minjuan Shi1, Junming Fu1, Shanshan Jiang4, Huiyao Yu1.   

Abstract

The cardioprotective drugs used for treatment against ischemia/reperfusion (MI/R) injury have been well evaluated and are considered inadequate. The Chinese herbal medicine formula, Xinji pill (XJP) has been used traditionally for the prevention and treatment of ischemic heart diseases for decades. In the present study, the cardioprotective effects of XJP against MI/R injury were assessed in vivo and its possible mechanism was examined. Male Sprague‑Dawley rats were selected for establishing an MI/R model, which was induced by ischemia for 30 min followed by 24 h reperfusion. Drugs and saline were administered intragastrically from day 14 prior to MI/R. Blood samples were collected for biochemical detection. The rats were then sacrificed and cardiac muscle tissues were harvested. The mRNA expression levels of antioxidant genes were measured by reverse transcription‑quantitative polymerase chain reaction and the protein levels were measured by western blotting. Pretreatment with XJP for 14 days protected the heart against I/R‑induced myocardial function disorder, protected against heart injury, as demonstrated by normalized serum levels of lactate dehydrogenase and creatine kinase, and suppressed oxidative stress. XJP markedly upregulated the expression of antioxidant genes, including superoxide dismutase, catalase, glutathione reductase and glutathione peroxidase, and promoted the protein expression of heme oxygenase‑1 and NFE2‑related factor 2 (Nrf2) in the heart tissues. Furthermore, Akt kinase was confirmed to be upstream of Nrf2 in the XJP treatment. LY294002, a specific inhibitor of Akt, significantly eliminated the cardioprotective effects of XJP. In conclusion, these results demonstrated that XJP exhibited notable cardioprotective properties, in which the Akt/Nrf2 signaling pathway may be involved.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28627591     DOI: 10.3892/mmr.2017.6732

Source DB:  PubMed          Journal:  Mol Med Rep        ISSN: 1791-2997            Impact factor:   2.952


  4 in total

1.  Vincamine prevents lipopolysaccharide induced inflammation and oxidative stress via thioredoxin reductase activation in human corneal epithelial cells.

Authors:  Li Wu; Meihong Ye; Jie Zhang
Journal:  Am J Transl Res       Date:  2018-07-15       Impact factor: 4.060

Review 2.  HyperCKemia associated with acupuncture: a case report and review of the literature.

Authors:  Xiaochan Tan; Wei Liu; Yuzheng Du; Xianggang Meng; Xuemin Shi
Journal:  BMC Complement Med Ther       Date:  2022-01-28

3.  Vincamine Modulates the Effect of Pantoprazole in Renal Ischemia/Reperfusion Injury by Attenuating MAPK and Apoptosis Signaling Pathways.

Authors:  Michael A Fawzy; Sherif A Maher; Mahmoud A El-Rehany; Nermeen N Welson; Nisreen K A Albezrah; Gaber El-Saber Batiha; Moustafa Fathy
Journal:  Molecules       Date:  2022-02-18       Impact factor: 4.411

4.  Cardioprotective effect of isorhamnetin against myocardial ischemia reperfusion (I/R) injury in isolated rat heart through attenuation of apoptosis.

Authors:  Yan Xu; Chun Tang; Shengyu Tan; Juan Duan; Hongmei Tian; Yu Yang
Journal:  J Cell Mol Med       Date:  2020-04-19       Impact factor: 5.310

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.