Abstract | BACKGROUND: 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.
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Authors | Binghui Zhao, Qing Zhao, Junhui Li, Tao Xing, Feng Wang, Niansong Wang |
Journal | PloS one
(PLoS One)
Vol. 10
Issue 1
Pg. e0116583
( 2015)
ISSN: 1932-6203 [Electronic] United States |
PMID | 25635854
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Contrast Media
- Protective Agents
- Triiodobenzoic Acids
- Creatinine
- Monoamine Oxidase
- renalase
- ioversol
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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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