Pioglitazone ameliorates renal ischemia reperfusion injury through NMDA receptor antagonism in rats

• Published in: Molecular and cellular biochemistry 2016-06, Vol.417 (1-2), p.111-118
• Main Authors: Singh, Amrit Pal, Singh, Nirmal, Bedi, Preet Mohinder Singh
• Format: Article
• Language: English
• Subjects: Animals; Aspartate; Biochemistry; Biomedical and Life Sciences; Cardiology; Glutamate; Ischemia; Kidney Diseases - metabolism; Kidney Diseases - prevention & control; Kidneys; Life Sciences; Male; Medical Biochemistry; Methyl aspartate; Oncology; Oxidative stress; Oxidizing agents; Rats; Rats, Wistar; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors; Receptors, N-Methyl-D-Aspartate - metabolism; Reperfusion injury; Reperfusion Injury - metabolism; Reperfusion Injury - prevention & control; Studies; Superoxide; Thiazolidinediones - pharmacology; Urea; Uric acid
• ISSN: 0300-8177; 1573-4919
• DOI: 10.1007/s11010-016-2718-x

The present study investigated the role of N -methyl- d -aspartate (NMDA) receptors in pioglitazone-mediated protection against renal ischemia reperfusion injury (IRI) in rats. Male wistar rats were subjected to 40 min of bilateral renal ischemia followed by reperfusion for 24 h to induce kidney injury. The renal damage was evaluated by measuring serum creatinine, creatinine clearance, blood urea nitrogen, uric acid, electrolytes, and microproteinuria in rats. Oxidative stress in renal tissues was quantified in terms of myeloperoxidase activity, thiobarbituric acid reactive substances, superoxide anion generation, and reduced glutathione level. Hematoxylin–eosin and periodic acid Schiff staining of renal tissues were performed to observe histological changes. Pioglitazone (20 and 40 mg/kg) was administered 1 h prior to ischemia in rats. In separate groups, NMDA agonists, glutamic acid (200 mg/kg), and spermidine (20 mg/kg) were administered 1 h prior to pioglitazone treatment, followed by renal IRI in rats. Ischemia reperfusion resulted in marked renal damage with significant changes in serum and urine parameters along with marked oxidative stress and histological changes in kidneys. Pioglitazone treatment afforded anti-oxidant effect and renoprotection in a dose-dependent manner in rats. Pioglitazone-mediated renoprotection was attenuated by glutamic acid and spermidine pretreatment in rats, which indicated the role of NMDA receptors in pioglitazone-mediated protection. It is concluded that NMDA antagonism serves as one of the mechanisms in pioglitazone-mediated protection against renal IRI in rats.