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Ethyl pyruvate is renoprotective against ischemia-reperfusion injury under hyperglycemia.
- Source :
-
The Journal of thoracic and cardiovascular surgery [J Thorac Cardiovasc Surg] 2018 Apr; Vol. 155 (4), pp. 1650-1658. Date of Electronic Publication: 2017 Nov 01. - Publication Year :
- 2018
-
Abstract
- Background: Hyperglycemia (HG) is common in cardiovascular surgeries due to diabetes, inflammation, and the neuroendocrine stress response. HG aggravates renal ischemia-reperfusion (I/R) injury through an increased inflammatory response, and blunts the protective effect of various measures. Ethyl pyruvate (EP) provides anti-inflammatory effects against I/R injury via inhibition of high-mobility group box 1 protein (HMGB1) release. This study aimed to determine the renoprotective effect of EP against I/R injury under HG.<br />Methods: Sprague-Dawley rats were randomly assigned at random to 8 groups: normoglycemia (NG)-sham, NG-I/R-control, NG-EP-I/R (pretreatment), NG-I/R-EP (posttreatment), HG-sham, HG-I/R-control, HG-EP-I/R, and HG-I/R-EP. Renal I/R was induced by 45 minutes of ischemia (clamping of renal arteries), followed by 24 hours of reperfusion. EP (50 mg/kg) was administered intraperitoneally at 1 h before ischemia (pretreatment) or on reperfusion (posttreatment).<br />Results: I/R injury under HG significantly aggravated the degree of renal tubular apoptosis and damage compared with the NG groups, which could be attenuated by both pretreatment and posttreatment of EP. I/R-induced increases in HMGB1 and Toll-like receptors (TLRs), activation of NF-kB, and resultant alterations in interleukin-1β, tumor necrosis factor-α, proapoptotic Bax, and antiapoptotic Bcl-2 were all favorably modulated by EP treatment in both the NG and HG groups compared with their corresponding control groups.<br />Conclusions: Despite aggravation of renal I/R injury by HG through amplified inflammation, EP administration showed similar suppression of the HMGB1-TLR-NF-kB pathway in the HG and NG groups. EP retained anti-inflammatory, antiapoptotic, and renoprotective effects in the HG groups, whether administered before ischemia or on reperfusion.<br /> (Copyright © 2017 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Apoptosis drug effects
Cytoprotection
Disease Models, Animal
HMGB1 Protein metabolism
Hyperglycemia blood
Hyperglycemia complications
Interleukin-1beta metabolism
Kidney metabolism
Kidney pathology
Kidney Diseases etiology
Kidney Diseases metabolism
Kidney Diseases pathology
Male
NF-kappa B metabolism
Proto-Oncogene Proteins c-bcl-2 metabolism
Rats, Sprague-Dawley
Reperfusion Injury etiology
Reperfusion Injury metabolism
Reperfusion Injury pathology
Signal Transduction drug effects
Toll-Like Receptors metabolism
Tumor Necrosis Factor-alpha metabolism
bcl-2-Associated X Protein metabolism
Anti-Inflammatory Agents pharmacology
Blood Glucose metabolism
Hyperglycemia drug therapy
Kidney drug effects
Kidney Diseases prevention & control
Pyruvates pharmacology
Reperfusion Injury prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1097-685X
- Volume :
- 155
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The Journal of thoracic and cardiovascular surgery
- Publication Type :
- Academic Journal
- Accession number :
- 29195627
- Full Text :
- https://doi.org/10.1016/j.jtcvs.2017.10.069