Asmaa F Hassan, Amal F Gharib, Howaida M Hagag, Khadiga A Ismail, Ola M Omran, Enshrah Modathir Elamin, Hebatallah Husseini Atteia
{"title":"在二硝基苯酚诱导缺氧的大鼠动物模型中服用黑升麻可恢复肾脏血液动力学和功能。","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":"{\"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. 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引用次数: 0
摘要
目的:缺氧是导致肾脏疾病的主要原因之一。本研究旨在评估黑升麻对二硝基苯酚(DNP)诱导的大鼠缺氧性肾损伤的影响:方法:本研究纳入了 40 只成年雄性大鼠。大鼠分为四组:对照组、茜草组、DNP 缺氧组和接受茜草(400 毫克/千克体重)的 DNP + 茜草组。测量血清和肾组织中促红细胞生成素(EPO)激素和缺氧诱导因子-2α(HIF-2α)水平。对肾氧化应激生物标志物、炎症生物标志物、肾血流动力学和组织病理学检查进行了评估:结果:与 DNP 缺氧大鼠相比,服用 N. sativa 能明显降低 DNP + N. sativa 治疗大鼠的血清 EPO 水平、HIF-2α(P < 0.001)。此外,通过降低肾组织丙二醛含量和提高超氧化物歧化酶、总硫醇和过氧化氢酶活性(各P < 0.001),它还极大地改善了肾氧化应激。此外,还观察到 DNP + N. sativa 大鼠的肾脏细胞间粘附分子-1、髓过氧化物酶和白细胞介素-6 有非常明显的下降(P < 0.001)。服用 N. sativa 后,肾血流动力学和肾功能也有所改善(所有参数的 P < 0.001)。此外,藜芦治疗减少了 DNP + 藜芦组的肾组织病理学变化。我们使用 Prism 软件包(GraphPad 8.0 版)对结果进行了统计分析:结论:藜芦对 DNP 引起的缺氧性肾损伤有缓解作用,并能恢复大鼠动物模型的肾功能。这些作用是通过抗氧化、抗炎和血液动力学机制实现的。
Restoration of renal hemodynamics and functions by Nigella sativa administration in dinitrophenol-induced hypoxia in rat's animal model.
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.