Trimetazidine prevents renal injury in the isolated perfused pig kidney exposed to prolonged cold ischemia

• Published in: Transplantation Vol. 64; no. 7; pp. 1082 - 1086
• Main Authors: HAUET, T, MOTHES, D, GOUJON, J.-M, CARITEZ, J. C, CARRETIER, M, LE MOYEC, L, EUGENE, M, TILLEMENT, J.-P
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott 15-10-1997; Lippincott, Williams & Wilkins
• Subjects: Adenosine; Allopurinol; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Animals; Biological and medical sciences; Clinical death. Palliative care. Organ gift and preservation; Glutathione; Hypertonic Solutions; In Vitro Techniques; Insulin; Ischemia; Kidney - cytology; Kidney - drug effects; Kidney - ultrastructure; Life Sciences; Lipid Peroxidation - drug effects; Magnetic Resonance Spectroscopy; Medical sciences; Organ Preservation - methods; Organ Preservation Solutions; Perfusion; Raffinose; Renal Circulation - drug effects; Reperfusion Injury - prevention & control; Swine; Trimetazidine - pharmacology; Graft(material); Experimental study; Trimetazidine; Kidney; Graft failure; Pig; Prevention; Vertebrata; Mammalia; Organ preservation; Reperfusion; Ischemia; Animal; Artiodactyla; Antiïschemic; Piperazine derivatives; Ungulata; Solution
• ISSN: 0041-1337; 1534-6080
• DOI: 10.1097/00007890-199710150-00025

Ischemia caused by cold storage (CS) and reperfusion of the kidney is often responsible for delayed graft function after transplantation. Significant attention has been focused on the cascade of events involved in ischemia-reperfusion injury, with the objective of identifying drugs to ameliorate the functional damage that occurs.
The purpose of this study was to evaluate the renal function of isolated perfused pig kidneys after 48 hr of CS with Euro-Collins (EC) solution plus trimetazidine (EC+TMZ), standard EC solution, or University of Wisconsin (UW) solution. Normothermic isolated perfused pig kidneys were randomized into five experimental groups: (A) control group (cold flush with cold heparinized saline and immediately reperfused; n=6); (B) cold flush with cold heparinized saline with TMZ (10(-6) M), n=6; (C) 48 hr of CS with EC and reperfusion (n=8); (D) 48 hr of CS with EC+TMZ alone and reperfusion (n=8); (E) 48 hr of CS with UW and reperfusion (n=8). Proton nuclear magnetic resonance spectroscopy and biochemical studies were performed for the functional evaluation during reperfusion. Lipid peroxidation was also determined. Histological examination (optical and electron microscopy) was performed after CS and reperfusion.
Using TMZ, the renal perfusate flow rate as well as the glomerular filtration rate and proximal tubular function were significantly improved. This improvement of renal function during reperfusion was correlated with a less significant cellular and interstitial edema. In addition, tubular injury markers were significantly lower in the group preserved with EC+TMZ, and TMZ reduced lipid peroxidation dramatically during reperfusion.
The addition of TMZ to the EC solution increased the preservation quality and renal tubular function, and gave protection from reperfusion injury better than EC alone or UW. These results strongly suggest that TMZ has a cytoprotective effect and may therefore be useful for kidney preservation.