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Cisplatin, a potent and prominent chemotherapeutic drug, has considerable side effects, including nephrotoxicity, which limits its therapeutic application and efficacy. Therefore, the development of agents that protect normal cells while preserving cisplatin's chemotherapeutic properties is of utmost importance. This study aimed to explore the protective effects of protein-rich extract (BBPE) against cisplatin-induced nephrotoxicity in a cisplatin-treated mouse model and human embryonic kidney (HEK293) cells. Apoptosis was assessed in HEK293 cells to determine the cytoprotective effects of BBPE and its effects on the generation of cisplatin-induced reactive oxygen species (ROS) and mitochondrial transmembrane potential (MTP) collapse. Although cisplatin induced nephrotoxicity in HEK293 cells, pretreatment with BBPE showed significant protective effects against cisplatin-induced nephrotoxicity by regulating the expression levels of pro- and antiapoptotic proteins. The cytoprotective effects of BBPE were mediated by decreased ROS production and MTP loss in cisplatin-treated HEK293 cells. The results were confirmed in the cisplatin-treated mouse model. Pretreatment with BBPE protected against cisplatin-induced nephrotoxicity by restoring malondialdehyde, superoxide dismutase, and catalase levels in kidney tissue and blood urea nitrogen and creatinine serum levels. Furthermore, histopathological assessment and terminal dUTP nick end-labeling staining showed that BBPE mitigated cisplatin-induced nephrotoxicity in kidney tissues. Overall, BBPE may act as a potent agent for alleviating cisplatin-induced nephrotoxicity, thereby increasing the safety of cisplatin-based chemotherapy.
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http://dx.doi.org/10.1089/jmf.2023.K.0182 | DOI Listing |
Biomed Pharmacother
September 2025
Toxicology Unit, Universidad de Salamanca, Edificio Departamental, Campus Miguel de Unamuno, Salamanca 37007, Spain; Institute of Biomedical Research of Salamanca (IBSAL), Paseo de San Vicente 182, Salamanca 37007, Spain; Group of Translational Research on Renal and Cardiovascular Diseases (TRECARD)
Immune checkpoint inhibitors (ICIs) represent a major advance in cancer treatment due to their efficacy and safety profile. However, they are not free of side effects, including nephrotoxicity, which worsens prognosis. Diagnosis of renal injury based on clinical findings has limitations in predicting and identifying the type of damage.
View Article and Find Full Text PDFAAPS Open
March 2025
Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Objective: Acute kidney injury (AKI) occurs in approximately one-third of patients treated with cisplatin and there is an outstanding need for mitigation strategies to decrease the frequency and severity of cisplatin-induced AKI. This study evaluated bardoxolone methyl (BARD) as a nephroprotectant in a multidose, tumor-bearing mouse model of cisplatin-induced AKI. BARD is an attractive therapeutic intervention due to its ability to protect against cisplatin-induced nephrotoxicity by activating Nrf2 and previous reports suggesting anti-tumorigenic effects.
View Article and Find Full Text PDFBasic Clin Pharmacol Toxicol
September 2025
Department of Pharmacology, Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, China.
Acute kidney injury (AKI) is a serious complication of cisplatin chemotherapy, with limited treatment options. In this study, we investigated the protective effects of wine-processed Polygonatum sibiricum (WP. P.
View Article and Find Full Text PDFToxicol Mech Methods
August 2025
Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
This study aimed to evaluate the nephroprotective effect of Cilostazol on Cisplatin-induced nephrotoxicity. Female Wistar albino rats were divided into four groups: normal, Cis (8 mg/kg), and two Cilostazol treatment groups (30 and 60 mg/kg) with cisplatin. Cisplatin application significantly deteriorated renal function- manifested by increased serum creatinine (261%) and BUN (134%)-and enhanced oxidative stress-characterized by increased MDA (234%) and decreased GSH (64%).
View Article and Find Full Text PDFFood Sci Nutr
August 2025
Division of Livestock Products Technology SKUAST-Jammu, J&K Jammu India.
The study aimed at gaining mechanistic insights into the modulation of cisplatin-induced (cDDP, 12 mg/kg-IP) renal toxicity by quercetin, catechin, and genistein in Wistar rats. Blood was analyzed for alterations in acute renal biomarkers (KIM-1, Cystatin-C, GGT, BUN, CR, UA) together with the changes in the activities of antioxidant biomarkers (TAS, TTH, GSH) and cellular damage indicators (MDA, AOPP and 8-OHdG). Additionally, alterations in the activities, variations in genetic expression of antioxidant enzymes (CAT, SOD, GPx, GST, AE, GR) and histomorphological lesions in the kidneys were studied.
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