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2,3,5,6-Tetramethylpyrazine (TMP) down-regulated arsenic-induced heme oxygenase-1 and ARS2 expression by inhibiting Nrf2, NF-kappa B, AP-1 and MAPK pathways in human proximal tubular cells  期刊论文  

  • 编号:
    1d01bd08-638f-4ea3-9916-25176760d1d2
  • 作者:
    Gong, Xuezhong(龚学忠)#*[1,2]Ivanov, Vladimir N.[2];Hei, Tom K.[2,3];
  • 语种:
    英文
  • 期刊:
    ARCHIVES OF TOXICOLOGY ISSN:0340-5761 2016 年 90 卷 9 期 (2187 - 2200) ; SEP
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  • 摘要:

    Our recent study demonstrated that sodium arsenite at a clinically relevant dose induced nephrotoxicity in human renal proximal tubular epithelial cell line HK-2, which could be inhibited by natural product 2,3,5,6-tetramethylpyrazine (TMP) with antioxidant activity. The present study demonstrated that arsenic exposure resulted in protein and enzymatic induction of heme oxygenase-1 (HO-1) in dose-and time-dependent manners in HK-2 cells. Blocking HO-1 enzymatic activity by zinc protoporphyrin (ZnPP) augmented arsenic-induced apoptosis, ROS production and mitochondrial dysfunction, suggesting a critical role for HO-1 as a renal protectant in this procession. On the other hand, TMP, upstream of HO-1, inhibited arsenic-induced ROS production and ROS-dependent HO-1 expression. TMP also prevented mitochondria dysfunction and suppressed activation of the intrinsic apoptotic pathway in HK-2 cells. Our results revealed that the regulation of arsenic-induced HO-1 expression was performed through multiple ROS-dependent signal pathways and the corresponding transcription factors, including p38 MAPK and JNK (but not ERK), AP-1, Nrf2 and NF-kappa B. TMP inhibited arsenic-induced activations of JNK, p38 MAPK, ERK, AP-1 and Nrf2 and block HO-1 protein expression. The present study, furthermore, demonstrated arsenic-induced expression of arsenic response protein 2 (ARS2) that was regulated by p38 MAPK, ERK and NF-kappa B. To our knowledge, this is the first report showing that ARS2 involved in arsenic-induced nephrotoxicity, while TMP pretreatment prevented such an up-regulation of ARS2 in HK-2 cells. Given ARS2 and HO-1 sharing the similar regulation mechanism, we speculated that ARS2 might also mediate cell survival in this procession. In summary, our study highlighted a role of HO-1 in the protection against arsenic-induced cytotoxicity downstream from the primary targets of TMP and further indicated that TMP may be used as a potential therapeutic agent in the treatment of arsenic-induced nephrotoxicity.

  • 推荐引用方式
    GB/T 7714:
    Gong Xuezhong,Ivanov Vladimir N.,Hei Tom K., et al. 2,3,5,6-Tetramethylpyrazine (TMP) down-regulated arsenic-induced heme oxygenase-1 and ARS2 expression by inhibiting Nrf2, NF-kappa B, AP-1 and MAPK pathways in human proximal tubular cells [J].ARCHIVES OF TOXICOLOGY,2016,90(9):2187-2200.
  • APA:
    Gong Xuezhong,Ivanov Vladimir N.,Hei Tom K..(2016).2,3,5,6-Tetramethylpyrazine (TMP) down-regulated arsenic-induced heme oxygenase-1 and ARS2 expression by inhibiting Nrf2, NF-kappa B, AP-1 and MAPK pathways in human proximal tubular cells .ARCHIVES OF TOXICOLOGY,90(9):2187-2200.
  • MLA:
    Gong Xuezhong, et al. "2,3,5,6-Tetramethylpyrazine (TMP) down-regulated arsenic-induced heme oxygenase-1 and ARS2 expression by inhibiting Nrf2, NF-kappa B, AP-1 and MAPK pathways in human proximal tubular cells" .ARCHIVES OF TOXICOLOGY 90,9(2016):2187-2200.
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