首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Protein kinase G-dependent heme oxygenase-1 induction by Agastache rugosa leaf extract protects RAW264.7 cells from hydrogen peroxide-induced injury.
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Protein kinase G-dependent heme oxygenase-1 induction by Agastache rugosa leaf extract protects RAW264.7 cells from hydrogen peroxide-induced injury.

机译:Ag香叶提取物诱导的蛋白激酶G依赖的血红素加氧酶-1可以保护RAW264.7细胞免受过氧化氢诱导的伤害。

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摘要

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.
机译:已经提出,可诱导的血红素加氧酶(HO)同工型可保护细胞免受氧化剂介导的损伤。尽管Ag香(Agastache rugosa)的成分表现出抗氧化作用,但尚不清楚该作用与HO-1活性有关。因此,我们调查了Ag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H(2)O(2)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HO-1蛋白和酶活性,并保护细胞免受H(2)O(2)诱导的细胞毒性,IC(50)为0.526 mg / ml。 HO-1诱导剂Hemin也显示出与ALE类似的作用。此外,HO抑制剂锌原卟啉IX抑制了ALE和血红素的保护作用。通过用鸟苷酸环化酶的特异性抑制剂LY83583和ODQ预处理,ALE可以降低HO-1蛋白的表达,但通过PKA抑制剂H89和KT5720可以降低HO-1蛋白的表达,表明PKG信号通路调节ALE诱导HO-1的表达。两者合计,得出结论,即依赖PKG的HO-1诱导是ALE保护RAW264.7细胞免受H(2)O(2)侵害的重要抗氧化剂机制之一。因此,ALE与其他作用一起可能对于治疗氧化剂引起的细胞损伤是有益的。

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