O K Yulizal, Darmadi Darmadi, Ok Ikram Alchair, Encik Nazifa Zanzabilla Putri, Wa Amalia Zahiah, Tesalonika Apmarda Simarmata
{"title":"Nephroprotective and antioxidant properties of a novel herbal extract combination in a high-fat diet and alloxan-induced kidney injury in rats.","authors":"O K Yulizal, Darmadi Darmadi, Ok Ikram Alchair, Encik Nazifa Zanzabilla Putri, Wa Amalia Zahiah, Tesalonika Apmarda Simarmata","doi":"10.5455/javar.2026.m1020","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objectives:</b> The present study investigated the therapeutic effects of a standardized capsule combination consisting of <i>Channa striata, Phyllanthus niruri</i> L., and <i>Curcuma xanthorrhiza</i> extracts (CCE) on biomarkers of kidney function, antioxidant status, and kidney histopathology in a high-fat diet (HFD) and alloxan-induced diabetic/nephrotoxic rat model. <b>Materials and Methods:</b> Male Wistar rats (<i>n</i> = 24) were divided into 4 groups: Control; HFD + alloxan treatment (diabetics/nephrotoxic); diabetics/nephrotoxic + CCE (49.5 mg/kg BW); diabetic/nephrotoxic + CCE + pioglitazone treatment group (1.35 mg/kg BW). Serum Cystatin C, superoxide dismutase (SOD) activity, and kidney histopathology were assessed at Day 60. <b>Results:</b> Model induction markedly increased blood glucose, HbA1c, and serum Cystatin C levels and decreased SOD activity (<i>p</i> < 0.001 vs controls). CCE significantly attenuated cystatin C by decreasing Cystatin C by 18.2% (<i>p</i> < 0.001) and restored SOD activity to 94.0% of control (<i>p</i> < 0.001). Histopathology showed marked improvements in glomerular hypertrophy, tubular injury, vascular congestion, and inflammatory infiltration (<i>p</i> < 0.001 vs model). CCE + pioglitazone showed comparable biochemical trends and enhanced histological preservation. <b>Conclusions:</b> CCE combination significantly attenuated diabetic/nephrotoxic-induced kidney injury by improving antioxidant defense and preserving kidney structure. This suggests therapeutic potential for managing metabolic kidney complications.</p>","PeriodicalId":14892,"journal":{"name":"Journal of Advanced Veterinary and Animal Research","volume":"13 1","pages":"159-169"},"PeriodicalIF":1.9000,"publicationDate":"2026-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13197731/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Veterinary and Animal Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5455/javar.2026.m1020","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: The present study investigated the therapeutic effects of a standardized capsule combination consisting of Channa striata, Phyllanthus niruri L., and Curcuma xanthorrhiza extracts (CCE) on biomarkers of kidney function, antioxidant status, and kidney histopathology in a high-fat diet (HFD) and alloxan-induced diabetic/nephrotoxic rat model. Materials and Methods: Male Wistar rats (n = 24) were divided into 4 groups: Control; HFD + alloxan treatment (diabetics/nephrotoxic); diabetics/nephrotoxic + CCE (49.5 mg/kg BW); diabetic/nephrotoxic + CCE + pioglitazone treatment group (1.35 mg/kg BW). Serum Cystatin C, superoxide dismutase (SOD) activity, and kidney histopathology were assessed at Day 60. Results: Model induction markedly increased blood glucose, HbA1c, and serum Cystatin C levels and decreased SOD activity (p < 0.001 vs controls). CCE significantly attenuated cystatin C by decreasing Cystatin C by 18.2% (p < 0.001) and restored SOD activity to 94.0% of control (p < 0.001). Histopathology showed marked improvements in glomerular hypertrophy, tubular injury, vascular congestion, and inflammatory infiltration (p < 0.001 vs model). CCE + pioglitazone showed comparable biochemical trends and enhanced histological preservation. Conclusions: CCE combination significantly attenuated diabetic/nephrotoxic-induced kidney injury by improving antioxidant defense and preserving kidney structure. This suggests therapeutic potential for managing metabolic kidney complications.