International Journal of Critical Illness and Injury Science · 2019 · 27 citations · 22 references
MedicinePharmacologyPharmacotherapyClinical PharmacologyRenal PathophysiologyRenal PharmacotherapyAcute Kidney InjuryRenal DiseaseRenal PharmacologyAcute Kidney Injury PathophysiologyAcute Kidney Injury PharmacotherapyDiclofenac TherapyDrug-induced Acute Kidney InjuryNeutrophil Gelatinase-associated LipocalinRenoprotective EffectsRenoprotective TherapiesSerum Creatinine Assessment
OBJECTIVE: To evaluate the renoprotective effects of berberine and/or pentoxifylline in reduction of diclofenac-induced acute kidney injury (AKI) in rats. MATERIAL AND METHODS: Fifty male Sprague-Dawley rats were allocated into five groups, Group 1: Rats treated with distilled water plus normal saline for 12 days. Group 2: Rats treated with distilled water plus diclofenac for 12 days. Group 3: Rats treated with berberine plus diclofenac for 12 days. Group 4: Rats treated with pentoxifylline plus diclofenac for 12 days. Group 5: Rats treated with berberine + pentoxifylline plus diclofenac 15 mg/kg for 12 days. Blood urea, creatinine, neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecules (KIM-1), and cystatin-c were used to measure the severity of AKI. RESULTS: Diclofenac led to significant AKI by significant elevation of blood urea, serum creatinine, KIM-1, and NGAL. Treatment with berberine showed no significant effect on all biomarkers level compared to diclofenac group except on serum KIM-1 level which also seen in the pentoxifylline group whereas combination of berberine and pentoxifylline led to more significant effect in the reduction of all renal biomarkers. CONCLUSION: Combination of berberine with pentoxifylline illustrated a synergistic effect in attenuation of diclofenac-induced AKI.
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