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Yang, B., Fu, J., Zheng, H., Xue, P., Yarborough, K., Woods, C.G., Hou, Y., Zhang, Q., Andersen, M.E. and Pi, J. (2012) Deficiency in the Nuclear Factor E2-Related Factor 2 Renders Pancreatic Beta-Cells Vulnerable to Arsenic-Induced Cell Damage. Toxicology and Applied Pharmacology, 264, 315-323.
https://doi.org/10.1016/j.taap.2012.09.012

has been cited by the following article:

• TITLE: Roles of Aqueous Extract of Marigold on Arsenic-Induced Oxidative Damage in Pancreatic Islet β-Cells

  AUTHORS: Zongqin Mei, Jiao Dai, Guofen Liu, Zuoshun He, Shiyan Gu

  KEYWORDS: Arsenic Trioxide, Marigold Extracts, Nuclear Factor E2-Related Factor 2, Oxidative Damage

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.12 No.5, May 8, 2024

  ABSTRACT: Roles of Marigold extracts (ME) on arsenic trioxide (ATO)-induced oxidative damage to pancreatic β-cells need to be further elucidated. In this study, NIT-1 cells were treated with different concentrations of and/or ATO, following by the cell viability was detected by CCK8 assay. Then, intracellular reactive oxygen species (ROS) levels, lipid peroxide (MDA) contents and superoxide dismutase (SOD) activity were measured with a fluorescence probe method and colorimetric assay, respectively. The apoptosis rate and morphology was detected and observed with hoechst 33,258 staining assay. The mRNA levels and protein expressions of nuclear factor E2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) were measured by real-time fluorescence quantitative polymerase chain reaction and protein immunoblotting assay, respectively. Our results indicated that Co-treatment with ME and ATO exacerbated the cell viability decreasing reduced by ATO, while the addition of ME after ATO treatment effectively promote the recovery of ATO reduced survival rates. The ATO group increased apoptosis (P P β-cells by modulating the activation of the Nrf2 signaling pathway.