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Renalase protects against contrast-induced nephropathy in Sprague-Dawley rats.

AbstractBACKGROUND:
Contrast-induced nephropathy (CIN) is the third leading cause of hospital-acquired acute renal failure. Oxidative stress, apoptosis and inflammation play crucial roles in CIN. Renalase is a newly discovered monoamine oxidase from the kidney. We hypothesize that renalase could protect against CIN through anti-oxidation, anti-inflammation and anti-apoptosis pathways.
METHODS:
We tested our hypothesis in vivo with a rat model of Ioversol-induced CIN and in vitro. Sprague-Dawley rats were divided into 4 groups (n = 6 per group): control group, Ioversol group (rats subjected to Ioversol-induced CIN), Ioversol plus vehicle group (CIN rats pretreated with vehicle) and Ioversol plus renalase group (CIN rats pretreated with 2 mg/kg recombinant renalase). HK2 cells were treated with Ioversol or H2O2.
RESULTS:
The results showed that pretreatment with renalase attenuated the deterioration of renal function, tubular necrosis, oxidative stress, apoptosis and inflammation (P<0.05). Furthermore, renalase protected HK2 cells against the cytotoxicity of Ioversol and suppressed Caspase-3 activity, oxidative stress and apoptosis induced by H2O2.
CONCLUSION:
Recombinant renalase protected CIN in rats through anti-oxidation, anti-apoptosis and anti-inflammation mechanisms.
AuthorsBinghui Zhao, Qing Zhao, Junhui Li, Tao Xing, Feng Wang, Niansong Wang
JournalPloS one (PLoS One) Vol. 10 Issue 1 Pg. e0116583 ( 2015) ISSN: 1932-6203 [Electronic] United States
PMID25635854 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Contrast Media
  • Protective Agents
  • Triiodobenzoic Acids
  • Creatinine
  • Monoamine Oxidase
  • renalase
  • ioversol
Topics
  • Animals
  • Apoptosis (drug effects)
  • Blood Urea Nitrogen
  • Contrast Media (adverse effects)
  • Creatinine (blood)
  • Inflammation (pathology)
  • Kidney (drug effects, pathology)
  • Kidney Diseases (blood, chemically induced, drug therapy, pathology)
  • Male
  • Monoamine Oxidase (pharmacology, therapeutic use)
  • Oxidative Stress (drug effects)
  • Protective Agents (pharmacology, therapeutic use)
  • Rats, Sprague-Dawley
  • Triiodobenzoic Acids (toxicity)

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