Asmaa F Hassan, Amal F Gharib, Howaida M Hagag, Khadiga A Ismail, Ola M Omran, Enshrah Modathir Elamin, Hebatallah Husseini Atteia
{"title":"Restoration of renal hemodynamics and functions by <i>Nigella sativa</i> administration in dinitrophenol-induced hypoxia in rat's animal model.","authors":"Asmaa F Hassan, Amal F Gharib, Howaida M Hagag, Khadiga A Ismail, Ola M Omran, Enshrah Modathir Elamin, Hebatallah Husseini Atteia","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Hypoxia is one of the principal causes of renal diseases. This study aimed to evaluate the effects of <i>Nigella sativa</i> on dinitrophenol (DNP)-induced hypoxia renal damage in rats.</p><p><strong>Methods: </strong>Forty adult male rats were incorporated in this study. The rats were divided into four groups: control group, <i>N. sativa</i> group, DNP hypoxic group, and DNP + <i>N. sativa</i> group receiving <i>N. sativa</i> (400 mg/kg body weight). Serum and renal tissue erythropoietin (EPO) hormone and hypoxia-inducible factor-2α (HIF-2α) levels were measured. Renal oxidative stress biomarkers, inflammatory biomarkers, renal hemodynamics, and histopathological examination were evaluated.</p><p><strong>Results: </strong>Administration of <i>N. sativa</i> highly significantly normalized serum EPO level, HIF-2α (<i>P</i> < 0.001 for each) in DNP + <i>N. sativa</i> treated rats as compared to DNP hypoxic rats. Furthermore, it highly significantly improved renal oxidative stress evident by decreased renal tissues malondialdehyde and increased superoxide dismutase, total thiol, and catalase activity (<i>P</i> < 0.001 for each). Furthermore, a highly significant decline of renal intercellular adhesion molecule-1, myeloperoxidase, and interleukin-6 was observed in DNP + <i>N. sativa</i> rats (<i>P</i> < 0.001 for each). Improvements in renal hemodynamics and kidney functions were also found after <i>N. sativa</i> administration (with <i>P</i> < 0.001 for all parameters). In addition, <i>N. sativa</i> treatment reduced renal histopathological changes of the DNP + <i>N. sativa</i> group. Our results were statistically analyzed using the Prism software package (GraphPad version 8.0).</p><p><strong>Conclusion: </strong><i>N. sativa</i> has an alleviating effect on DNP-induced hypoxia renal damage and can restore kidney functions in rats' animal models. These effects were through antioxidant, anti-inflammatory, and hemodynamic mechanisms.</p>","PeriodicalId":47093,"journal":{"name":"International Journal of Health Sciences-IJHS","volume":"18 4","pages":"22-31"},"PeriodicalIF":2.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11226942/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Health Sciences-IJHS","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Hypoxia is one of the principal causes of renal diseases. This study aimed to evaluate the effects of Nigella sativa on dinitrophenol (DNP)-induced hypoxia renal damage in rats.
Methods: Forty adult male rats were incorporated in this study. The rats were divided into four groups: control group, N. sativa group, DNP hypoxic group, and DNP + N. sativa group receiving N. sativa (400 mg/kg body weight). Serum and renal tissue erythropoietin (EPO) hormone and hypoxia-inducible factor-2α (HIF-2α) levels were measured. Renal oxidative stress biomarkers, inflammatory biomarkers, renal hemodynamics, and histopathological examination were evaluated.
Results: Administration of N. sativa highly significantly normalized serum EPO level, HIF-2α (P < 0.001 for each) in DNP + N. sativa treated rats as compared to DNP hypoxic rats. Furthermore, it highly significantly improved renal oxidative stress evident by decreased renal tissues malondialdehyde and increased superoxide dismutase, total thiol, and catalase activity (P < 0.001 for each). Furthermore, a highly significant decline of renal intercellular adhesion molecule-1, myeloperoxidase, and interleukin-6 was observed in DNP + N. sativa rats (P < 0.001 for each). Improvements in renal hemodynamics and kidney functions were also found after N. sativa administration (with P < 0.001 for all parameters). In addition, N. sativa treatment reduced renal histopathological changes of the DNP + N. sativa group. Our results were statistically analyzed using the Prism software package (GraphPad version 8.0).
Conclusion: N. sativa has an alleviating effect on DNP-induced hypoxia renal damage and can restore kidney functions in rats' animal models. These effects were through antioxidant, anti-inflammatory, and hemodynamic mechanisms.