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藿香叶提取物通过蛋白激酶G依赖性诱导血红素加氧酶-1保护RAW264.7细胞免受过氧化氢诱导的损伤。

Protein kinase G-dependent heme oxygenase-1 induction by Agastache rugosa leaf extract protects RAW264.7 cells from hydrogen peroxide-induced injury.

作者信息

Oh Hwa Min, Kang Young Jin, Lee Young Soo, Park Min Kyu, Kim Sun Hee, Kim Hye Jung, Seo Han Geuk, Lee Jae Heun, Chang Ki Churl

机构信息

Department of Pharmacology, School of Medicine, Institute of Health Sciences, Gyeongsang National University, 92 Chilam-dong, Jinju 660-751, South Korea.

出版信息

J Ethnopharmacol. 2006 Jan 16;103(2):229-35. doi: 10.1016/j.jep.2005.08.030. Epub 2005 Sep 26.

Abstract

It has been proposed that the inducible isoform of heme oxygenase (HO) protects cells against oxidant-mediated injury. Although components of Agastache rugosa showed antioxidant effect, it is unclear this effect is related with HO-1 activity. Thus, we investigated the effects of Agastache rugosa leaf extract (ALE) on HO-1 protein expression and enzyme activity, and its protective effect against H(2)O(2)-induced oxidative damage was also investigated using RAW264.7 macrophage cells. Results showed that ALE concentration dependently increased HO-1 protein and enzyme activity, and protected cells from H(2)O(2)-induced cytotoxicity, with an IC(50) of 0.526 mg/ml. Hemin, a HO-1 inducer, also showed similar effect to ALE. Furthermore, the protective effect of both ALE and hemin was inhibited by a HO inhibitor, zinc protoporphyrin IX. The expression of HO-1 protein by ALE was reduced by pretreatment with LY83583 and ODQ, specific inhibitors of guanylate cyclase, but not by PKA inhibitors, H89 and KT5720, indicating that PKG signaling pathway regulates HO-1 induction by ALE. Taken together, it is concluded that PKG-dependent HO-1 induction is one of the important antioxidant mechanisms by which ALE protects RAW264.7 cells from H(2)O(2). Thus, ALE along with other actions may be beneficial for the treatment of oxidant-induced cellular injuries.

摘要

有人提出,血红素加氧酶(HO)的诱导型同工型可保护细胞免受氧化介导的损伤。虽然藿香的成分显示出抗氧化作用,但尚不清楚这种作用是否与HO-1活性有关。因此,我们研究了藿香叶提取物(ALE)对HO-1蛋白表达和酶活性的影响,并使用RAW264.7巨噬细胞研究了其对H₂O₂诱导的氧化损伤的保护作用。结果表明,ALE浓度依赖性地增加了HO-1蛋白和酶活性,并保护细胞免受H₂O₂诱导的细胞毒性,IC₅₀为0.526 mg/ml。HO-1诱导剂血红素对ALE也有类似作用。此外,HO抑制剂原卟啉锌IX抑制了ALE和血红素的保护作用。用鸟苷酸环化酶的特异性抑制剂LY83583和ODQ预处理可降低ALE诱导的HO-1蛋白表达,但蛋白激酶A抑制剂H89和KT5720则无此作用,这表明蛋白激酶G信号通路调节ALE诱导的HO-1。综上所述,得出结论:PKG依赖性HO-1诱导是ALE保护RAW264.7细胞免受H₂O₂损伤的重要抗氧化机制之一。因此,ALE与其他作用一起可能对治疗氧化诱导的细胞损伤有益。

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