Sukru Ulusoy1, Gulsum Ozkan2, Sevdegül Mungan3, Asım Orem4, Esin Yulug5, Mehmet Alkanat6, Fulya Balaban Yucesan4. 1. Department of Nephrology, Karadeniz Technical University, School of Medicine, Trabzon, Turkey. Electronic address: sulusoy2002@yahoo.com. 2. Department of Nephrology, Karadeniz Technical University, School of Medicine, Trabzon, Turkey. 3. Department of Pathology, Karadeniz Technical University, School of Medicine, Trabzon, Turkey. 4. Department of Biochemistry, Karadeniz Technical University, School of Medicine, Trabzon, Turkey. 5. Department of Histology and Embryology, Karadeniz Technical University, School of Medicine, Trabzon, Turkey. 6. Department of Physiology, Karadeniz Technical University, School of Medicine, Trabzon, Turkey.
Abstract
AIMS: Our study was intended to evaluate the role of inducible nitric oxide synthase (iNOS), endothelial nitric oxide synthase (eNOS), caspases 1 and 3 and calpain 1 in the pathogenesis of contrast-induced nephropathy (CIN) and to compare the protective effects of N acetyl cysteine (NAC) and grape seed proanthocyanidin extract (GSPE) against the development of CIN. MAIN METHODS: 32 rats were divided into four groups; control, contrast media (CM), CM+NAC and CM+GSPE. CIN was induced by administration of 7 ml/kg diatrizoate. The experiment was discontinued on the ninth day. Blood was collected for blood urea nitrogen (BUN) and creatinine measurement. Rat kidney tissues were removed for histopathological evaluation and the investigation of caspases 1 and 3, iNOS, eNOS, TUNEL and calpain 1. KEY FINDINGS: A significant increase in BUN, creatinine, renal histopathological injury, TUNEL, caspases 1, 3, calpain 1, iNOS and eNOS was observed in the CM group compared to the control group. There was amelioration in all these parameters in the CM+GSPE group, while there was no significant amelioration in BUN, creatinine and renal histopathological injury in the CM+NAC group. In addition, calpain 1 staining and creatinine were significantly lower in the CM+GSPE group compared to the CM+NAC group. SIGNIFICANCE: Our study showed, for the first time in the literature, that GSPE has a greater renoprotective effect compared with NAC and that this effective protection may be related to decrease in calpain 1 levels.
AIMS: Our study was intended to evaluate the role of inducible nitric oxide synthase (iNOS), endothelial nitric oxide synthase (eNOS), caspases 1 and 3 and calpain 1 in the pathogenesis of contrast-induced nephropathy (CIN) and to compare the protective effects of N acetyl cysteine (NAC) and grape seed proanthocyanidin extract (GSPE) against the development of CIN. MAIN METHODS: 32 rats were divided into four groups; control, contrast media (CM), CM+NAC and CM+GSPE. CIN was induced by administration of 7 ml/kg diatrizoate. The experiment was discontinued on the ninth day. Blood was collected for blood ureanitrogen (BUN) and creatinine measurement. Rat kidney tissues were removed for histopathological evaluation and the investigation of caspases 1 and 3, iNOS, eNOS, TUNEL and calpain 1. KEY FINDINGS: A significant increase in BUN, creatinine, renal histopathological injury, TUNEL, caspases 1, 3, calpain 1, iNOS and eNOS was observed in the CM group compared to the control group. There was amelioration in all these parameters in the CM+GSPE group, while there was no significant amelioration in BUN, creatinine and renal histopathological injury in the CM+NAC group. In addition, calpain 1 staining and creatinine were significantly lower in the CM+GSPE group compared to the CM+NAC group. SIGNIFICANCE: Our study showed, for the first time in the literature, that GSPE has a greater renoprotective effect compared with NAC and that this effective protection may be related to decrease in calpain 1 levels.
Authors: Laura Vicente-Vicente; David González-Calle; Alfredo Ginés Casanova; María Teresa Hernández-Sánchez; Marta Prieto; Juan Carlos Rama-Merchán; Javier Martín-Moreiras; Francisco Martín-Herrero; Pedro Luis Sánchez; Francisco J López-Hernández; Ignacio Cruz-González; Ana Isabel Morales Journal: Int J Mol Sci Date: 2019-10-08 Impact factor: 5.923