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Leptin Alleviates Inflammatory Response in Myocardial Ischemia Reperfusion Injury.
- Source :
-
Disease markers [Dis Markers] 2022 Mar 09; Vol. 2022, pp. 8707061. Date of Electronic Publication: 2022 Mar 09 (Print Publication: 2022). - Publication Year :
- 2022
-
Abstract
- Objective: To investigate the role of leptin in regulating cell inflammation and protecting myocardium after myocardial ischemia-reperfusion injury in rats through signaling pathway at tissue and molecular protein levels.<br />Methods: Healthy female SD rats were randomly divided into 4 groups, which were sham, I/R group, leptin low-dose intervention group, and high-dose intervention group (40 μ g/kg and 80 μ g/kg, respectively). Cardiac hemodynamics, myocardial enzymology, inflammatory indices, and pathological changes were observed. Western blot was used to observe the expression of PI3K, AKT, and NF κ B protein by leptin.<br />Results: Leptin can improve the hemodynamics of cardiac ischemia-reperfusion rats, improve the expression of myocardial enzymology, reduce the release of cardiac and serum inflammatory factors, increased PI3k, AKT, and NF κ B expression, and reduce the occurrence of inflammation from the perspective of gross pathology, thus protecting the body.<br />Conclusion: Leptin pretreatment can reduce MIRI injury, and the protective mechanism may be that leptin upregulates PI3K-AKT-NF κ B expression in myocardial tissue to reduce inflammation and promote repair of I/R injury.<br />Competing Interests: The authors declare that they have no conflicts of interest.<br /> (Copyright © 2022 Shu Xu and Dengshun Tao.)
- Subjects :
- Animals
Class Ib Phosphatidylinositol 3-Kinase
Female
Myocardium enzymology
Phosphatidylinositol 3-Kinases metabolism
Proto-Oncogene Proteins c-akt metabolism
Rats
Rats, Sprague-Dawley
Signal Transduction
Inflammation metabolism
Leptin immunology
Leptin metabolism
Myocardial Reperfusion Injury drug therapy
Myocardial Reperfusion Injury metabolism
Protective Agents
Subjects
Details
- Language :
- English
- ISSN :
- 1875-8630
- Volume :
- 2022
- Database :
- MEDLINE
- Journal :
- Disease markers
- Publication Type :
- Academic Journal
- Accession number :
- 35308138
- Full Text :
- https://doi.org/10.1155/2022/8707061