柠檬草精油和柠檬醛对双氯芬酸所致小鼠毒性的肾脏保护和肝脏保护作用

Mohaddeseh Abouhosseini Tabari, Masoumeh Houshyar, Atefeh Araghi, Navideh Mirzakhani, Giuseppe Crescenzo, Roberta Cardone, Claudia Zizzadoro
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摘要

本研究旨在评估和比较两种著名的草本抗氧化剂在小鼠急性 DIC 引起的肾脏和肝脏毒性模型中的保护潜力。测试的抗氧化剂包括柠檬草精油(LO)及其主要生物活性成分柠檬醛(CIT)。第三种草药产品水飞蓟素(SILY)被用作参考肝肾保护剂。服用 DIC 会导致血清尿素和肌酐水平升高,并引发氧化应激和肾组织病理变化。与此同时,服用 DIC 会增加血清肝酶活性,降低总蛋白、白蛋白和球蛋白水平,并引起氧化应激和相关的肝组织病理变化。预处理 LO 或 CIT 可减轻 DIC 引起的所有肝肾健康血清生化指标的变化(白蛋白除外)。在肾脏和肝脏组织中,大剂量 LO 与 SILY 一样,可抵消 DIC 引起的氧化应激和组织形态学改变。相比之下,CIT 未能减轻 DIC 在肾脏中诱导的氧化应激,只能部分控制 DIC 在肝脏中诱导的氧化应激,因此与 LO 相比,CIT 对肾功能和肝脏结构完整性的保护效果较差。除了证实 SILY 在不同于迄今为止测试过的啮齿类物种(大鼠)中具有保护肾脏和肝脏免受 DIC 毒性影响的功效外,这项研究还证明了 LO 以及(在较小程度上)CIT 对小鼠体内 DIC 引起的肝肾毒性具有预防特性,从而支持了它们作为治疗药物的发展潜力。
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Nephroprotective and hepatoprotective effects of lemongrass essential oil and citral on diclofenac-induced toxicity in mice.

The present study was carried out to evaluate and compare the protective potential of two well-known antioxidants of herbal origin in a mouse model of acute DIC-induced nephro- and hepatotoxicity. The tested antioxidants included lemongrass essential oil (LO) and its predominant bioactive constituent citral (CIT). A third herbal product, silymarin (SILY), was used as a reference hepato-renal protective agent. DIC administration led to elevated serum urea and creatinine levels, and prompted oxidative stress along with histopathological changes in the kidney tissue. In parallel, DIC administration increased serum liver enzyme activity, decreased total protein, albumin, and globulin levels, and caused oxidative stress with associated histopathological changes in the liver tissue. Pre-treatment with LO or CIT mitigated DIC-induced alterations in all serum biochemical markers of kidney and liver health (except albumin). High-dose LO, like SILY, within kidney and liver tissues, counteracted DIC-induced oxidative stress and histomorphological alterations. By contrast, CIT failed to mitigate DIC-induced oxidative stress in the kidneys and provided only partial control of DIC-induced oxidative stress in the liver, resulting in less efficient preservation of kidney function and liver structural integrity than LO. Besides confirming the efficacy of SILY at protecting kidneys and liver against the toxicity of DIC in a rodent species different from the one tested so far (rat), this study demonstrated the preventive properties of LO and, to a lesser extent, of CIT against DIC-induced hepato-renal toxicity in mice, supporting their developmental potential as therapeutics.

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