4.7 Review

Insights into the mechanisms of arsenic-selenium interactions and the associated toxicity in plants, animals, and humans: A critical review

Journal

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/10643389.2020.1740042

Keywords

Arsenic-selenium; complex-interactions; toxicity

Funding

  1. National Key Research and Development Program of China [2019 YFC1803600, 2017YFD0800302]
  2. National Science Foundation of China-Project of Karst Science Research Center [U1612442]
  3. Science and Technology program of Guizhou Province [(2019)5618/2019(2963)/(2019)4428]
  4. UK NERC [NE/R013349/2]
  5. Royal Academy of Engineering seed grant [FoDSF\1819\1\8]
  6. EPSRC [EP/P017460/1] Funding Source: UKRI
  7. NERC [NE/R013349/2, NE/R013349/1] Funding Source: UKRI

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This review discusses the sources, uptake, and toxicity of arsenic and selenium in the environment, focusing on their interactions in plants, animals, and humans. The interaction between arsenic and selenium is crucial for understanding the transport and toxicological effects of these metals in biological systems.
This review highlights arsenic (As) and selenium (Se) sources in the environment, their uptake in the soil-plant system, interactions between these metals and the associated toxicity in major biological compartments, which may assist in addressing the hazardous impacts associated with As and Se contamination. The interaction between As and Se is a critical factor for a detailed systematic understanding of the transportation, environmental fate, and associated toxicological effects of these metalloids in plants, animals, and humans. Arsenic and Se induce cytotoxicity and genotoxicity through the generation of reactive oxygen species (ROS). Compared to arsenite (As-III), methylated arsenicals, including methylarsonous acid (MAsIII) and dimethylarsinous acids (DMAsIII), exhibit more cytotoxic and genotoxic potential to inhibit more potent enzymes and activate the protein AP & x2d7;1, which is a critical marker of genetic stability. Methylated As-III and its associated metabolites are well-known potential carcinogens that induce toxicity by blocking Se metabolism pathway. The imbalance of Se compounds can lead to the generation of ROS, which can inhibit or decrease genomic stability. The As and Se nexus also affect cellular signaling through activation of transcription factors such as NF kappa B and AP-1.

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