» Articles » PMID: 9202547

Ischaemia-reperfusion Injury in the Rat Kidney: the Effect of Preconditioning

Overview
Journal Br J Urol
Specialty Urology
Date 1997 Jun 1
PMID 9202547
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: To design and establish a model to examine whether brief periods of renal artery occlusion (ischaemic preconditioning, IP) confers protection from the effects of a subsequent period of ischaemia and reperfusion of the rat kidney.

Materials And Methods: Ninety rats were randomized into six groups, i.e. sham-operated controls; IP alone; a 20 or 40 min period of left renal ischaemia (RI) alone; and IP followed by a 20 or 40 min period of RI. Preconditioning involved the sequential clamping of the left renal artery for 4 min and its release for 11 min, a total of four times, a 'critical interval' of 30 min before the ischaemic insult. Left renal tissue integrity was determined by dimercapto-succinic acid (DMSA) radionuclide imaging on a gamma-camera both immediately (day 0) and 2 and 9 days later. Acute tubular necrosis was also assessed histologically.

Results: RI for 20 min resulted in a significant decrease in left renal tissue integrity on day 2 only (P < 0.001), whereas RI for 40 min caused significant left renal dysfunction on day 0, day 2 and day 9 (P < or = 0.01). For a given duration of ischaemia, there was no significant difference between results from (IP + RI) rats compared with RI-only rats at any of the three times. There was no significant alteration in renal tissue integrity in the IP-only rats compared with sham-operated controls. Histological findings paralleled the data obtained from DMSA uptake.

Conclusions: The IP regimen and 30 min 'critical interval' confers no protection to the kidney from a 20 or 40 min ischaemic episode. The IP regimen itself appears to have no effect, confirming the validity of our experimental model.

Citing Articles

Sulfotransferase 1C2 Increases Mitochondrial Respiration by Converting Mitochondrial Membrane Cholesterol to Cholesterol Sulfate.

Kolb A, Corridon P, Ullah M, Pfaffenberger Z, Xu W, Winfree S Biochemistry. 2024; 63(18):2310-2322.

PMID: 39194960 PMC: 11411706. DOI: 10.1021/acs.biochem.3c00344.


LncR-GAS5 decrease in adenine phosphoribosyltransferase expresssion via binding TAF1 to increase kidney damage created by CIH.

Liu W, Liang W, Zhang C, Liu H, Li H, Zhou L Heliyon. 2024; 10(12):e33084.

PMID: 38994083 PMC: 11238052. DOI: 10.1016/j.heliyon.2024.e33084.


Nitric Oxide in Cardiac Surgery: A Review Article.

Kamenshchikov N, Duong N, Berra L Biomedicines. 2023; 11(4).

PMID: 37189703 PMC: 10135597. DOI: 10.3390/biomedicines11041085.


Ouabain-Induced Cell Death and Survival. Role of α1-Na,K-ATPase-Mediated Signaling and [Na]/[K]-Dependent Gene Expression.

Lopina O, Tverskoi A, Klimanova E, Sidorenko S, Orlov S Front Physiol. 2020; 11:1060.

PMID: 33013454 PMC: 7498651. DOI: 10.3389/fphys.2020.01060.


Targeting HIF-1 to Prevent Renal Ischemia-Reperfusion Injury: Does It Work?.

Sethi K, Rao K, Bolton D, Patel O, Ischia J Int J Cell Biol. 2019; 2018:9852791.

PMID: 30595695 PMC: 6286753. DOI: 10.1155/2018/9852791.