CLC number: R58
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2014-05-26
Cited: 4
Clicked: 8297
Sheng-hong Zhu, Li-jia Zhou, Hong Jiang, Rong-jun Chen, Chuan Lin, Shi Feng, Juan Jin, Jiang-hua Chen, Jian-yong Wu. Protective effect of indomethacin in renal ischemia-reperfusion injury in mice[J]. Journal of Zhejiang University Science B, 2014, 15(8): 735-742.
@article{title="Protective effect of indomethacin in renal ischemia-reperfusion injury in mice",
author="Sheng-hong Zhu, Li-jia Zhou, Hong Jiang, Rong-jun Chen, Chuan Lin, Shi Feng, Juan Jin, Jiang-hua Chen, Jian-yong Wu",
journal="Journal of Zhejiang University Science B",
volume="15",
number="8",
pages="735-742",
year="2014",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1300196"
}
%0 Journal Article
%T Protective effect of indomethacin in renal ischemia-reperfusion injury in mice
%A Sheng-hong Zhu
%A Li-jia Zhou
%A Hong Jiang
%A Rong-jun Chen
%A Chuan Lin
%A Shi Feng
%A Juan Jin
%A Jiang-hua Chen
%A Jian-yong Wu
%J Journal of Zhejiang University SCIENCE B
%V 15
%N 8
%P 735-742
%@ 1673-1581
%D 2014
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1300196
TY - JOUR
T1 - Protective effect of indomethacin in renal ischemia-reperfusion injury in mice
A1 - Sheng-hong Zhu
A1 - Li-jia Zhou
A1 - Hong Jiang
A1 - Rong-jun Chen
A1 - Chuan Lin
A1 - Shi Feng
A1 - Juan Jin
A1 - Jiang-hua Chen
A1 - Jian-yong Wu
J0 - Journal of Zhejiang University Science B
VL - 15
IS - 8
SP - 735
EP - 742
%@ 1673-1581
Y1 - 2014
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1300196
Abstract: Objective: To evaluate the renoprotection effects of non-steroidal anti-inflammatory drugs (NSAIDs) in renal ischemia-reperfusion injury (IRI) and the cyclooxygenase (COX)-1/2 blockade association by indomethacin (IMT) in the mice model. Methods: After the left renal pedicle of mice was clamped, IMT was administrated by intraperitoneal injection with four doses: 1, 3, 5, and 7 mg/kg. Blood and kidney samples were collected 24 h after IRI. The renal functions were assayed by the cytokines and serum creatinine (SCr) using enzyme-linked immunosorbent assay (ELISA) kits. Kidney samples were analyzed by hematoxylin and eosin (H&E) and immunohistochemistry stainings. Results: The mice administered with 5 mg/kg IMT had a marked reduction in SCr and significantly less tubular damage. The tumor necrosis factor α (TNF-α) activity in renal homogenates and interleukin 6 (IL-6) activity in serum had a marked reduction at doses of 5 and 7 mg/kg IMT. The administration of 3 and 5 mg/kg IMT had a marked reduction in the ratio of thromboxane B2 to 6-keto-prostaglandin F1α. COX-1 and COX-2 stainings were weaker in 5 mg/kg IMT groups than that in the other groups. Conclusions: There was a dose response in the IMT function of renal IRI in mice, and IMT had a protective effect in a certain dose range. The effect of IMT on mice IRI was related to COX-1/2 blockades.
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