Department of Agricultural Biotechnology, Faculty of Agriculture, Ataturk University, Erzurum, Turkey.
Department of Biology, Faculty of Science, Atatürk University, Erzurum, Turkey.
J Food Biochem. 2021 Feb;45(2):e13628. doi: 10.1111/jfbc.13628. Epub 2021 Jan 27.
We evaluated the ameliorative role of umbelliferone in kidney, heart, and lung damage induced by renal ischemia/reperfusion (I/R) injury in rats. Umbelliferone was given orally to rats 60 min before ischemia. Ischemia was induced for 50 min and then reperfusion for 3 hr. The antioxidant enzymes, myeloperoxidase (MPO) activity, malondialdehyde (MDA) content, and cytokine levels in the kidney, heart, and lung were measured by ELISA. Moreover, histopathological changes were monitored. Renal I/R-induced oxidative stress in the organs by decreasing antioxidant enzymes. However, umbelliferone pretreatment enhanced superoxide dismutase (SOD) and glutathione (GSH), levels, reduced MDA and MPO levels. Renal I/R increased in tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6) levels, and histopathological changes but these effects were inhibited with umbelliferone pretreatment. Furthermore, umbelliferone increased in nitric oxide synthase (eNOS) level under ischemia conditions. Our results indicated that pretreatment of umbelliferone-ameliorated damages in remote organ induced by renal I/R through suppressing oxidative stress and modulating inflammatory responses. PRACTICAL APPLICATIONS: kidney, heart, and lung damages induced by renal I/R in rats was alleviated by umbelliferone. The oral treatment of umbelliferone markedly reversed the oxidative stress, inflammation, and histopathological changes by increasing in the levels of SOD, GSH, and eNOS, decreasing in the levels of MDA, MPO, TNF-α, and IL-6 in distant organ injury induced by renal I/R. This study firstly revealed that umbelliferone has potent antioxidant and anti-inflammatory activity in the remote organ damages caused by renal I/R. Consequently, umbelliferone may be an alternative therapeutic agent for treating renal I/R-induced damages.
我们评估了伞形酮对肾缺血/再灌注(I/R)损伤诱导的大鼠肾、心、肺损伤的改善作用。伞形酮在缺血前 60 分钟经口给予大鼠。缺血 50 分钟,然后再灌注 3 小时。通过 ELISA 测定肾、心、肺组织中的抗氧化酶、髓过氧化物酶(MPO)活性、丙二醛(MDA)含量和细胞因子水平。此外,还监测了组织病理学变化。肾 I/R 通过降低抗氧化酶在器官中引起氧化应激。然而,伞形酮预处理增强了超氧化物歧化酶(SOD)和谷胱甘肽(GSH)水平,降低了 MDA 和 MPO 水平。肾 I/R 增加肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)水平和组织病理学变化,但这些作用被伞形酮预处理抑制。此外,伞形酮在缺血条件下增加了一氧化氮合酶(eNOS)水平。我们的结果表明,伞形酮预处理通过抑制氧化应激和调节炎症反应,改善肾 I/R 引起的远隔器官损伤。实际应用:伞形酮减轻了肾 I/R 诱导的大鼠肾、心、肺损伤。伞形酮的口服治疗通过增加 SOD、GSH 和 eNOS 的水平,降低 MDA、MPO、TNF-α和 IL-6 的水平,显著逆转了氧化应激、炎症和组织病理学变化,从而显著逆转了由肾 I/R 引起的远隔器官损伤。这项研究首次表明,伞形酮在肾 I/R 引起的远隔器官损伤中具有强大的抗氧化和抗炎活性。因此,伞形酮可能是治疗肾 I/R 诱导损伤的一种替代治疗药物。