Abstract | BACKGROUND: METHODS: Renal ischemia-reperfusion injury was induced in male C57BL/6 mice by bilateral renal pedicle occlusion for 30 minutes, followed by reperfusion for 48 hours. PDRN (8 mg/kg body weight intraperitoneally) was administered 30 minutes before IRI. RESULTS: CONCLUSIONS: Our findings suggest that PDRN is a potential therapeutic agent for acute ischemia-induced renal damage.
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Authors | E K Jeong, H J Jang, S S Kim, S Y Lee, M Y Oh, H J Kim, D W Eom, J Y Ham, D J Han |
Journal | Transplantation proceedings
(Transplant Proc)
Vol. 48
Issue 4
Pg. 1251-7
(May 2016)
ISSN: 1873-2623 [Electronic] United States |
PMID | 27320598
(Publication Type: Journal Article)
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Copyright | Copyright © 2016 Elsevier Inc. All rights reserved. |
Chemical References |
- Biomarkers
- Polydeoxyribonucleotides
- Protective Agents
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Topics |
- Acute Kidney Injury
(diagnosis, etiology, metabolism, prevention & control)
- Animals
- Biomarkers
(metabolism)
- Kidney Transplantation
- Male
- Mice
- Mice, Inbred C57BL
- Polydeoxyribonucleotides
(therapeutic use)
- Protective Agents
(therapeutic use)
- Random Allocation
- Reperfusion Injury
(diagnosis, metabolism, prevention & control)
- Treatment Outcome
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