Toxic Effects of Bisphenol A, Propyl Paraben, and Triclosan on Caenorhabditis elegans.
María Cecilia García-EspiñeiraLesly Patricia Tejeda-BenítezJesús Olivero-VerbelPublished in: International journal of environmental research and public health (2018)
Bisphenol A (BPA) is a ubiquitous plasticizer which is absorbed by ingestion and dermal contact; propyl paraben (PPB) inhibits the microbiome and extends the shelf life of many personal care products, whereas triclosan (TCS) is commonly found in antiseptics, disinfectants, or additives. In this work, Caenorhabditis elegans was used as a biological model to assess the toxic effects of BPA, PPB, and TCS. The wild type strain, Bristol N2, was used in bioassays with the endpoints of lethality, growth, and reproduction; green fluorescent protein (GFP) transgenic strains with the hsp-3, hsp-4, hsp-16.2, hsp-70, sod-1, sod-4, cyp-35A4, cyp-29A2, and skn-1 genes were evaluated for their mRNA expression through fluorescence measurement; and quick Oil Red O (q ORO) was utilized to stain lipid deposits. Lethality was concentration-dependent, while TCS and PPB showed more toxicity than BPA. BPA augmented worm length, while PPB reduced it. All toxicants moderately increased the width and the width-length ratio. BPA and PPB promoted reproduction, in contrast to TCS, which diminished it. All toxicants affected the mRNA expression of genes related to cellular stress, control of reactive oxygen species, and nuclear receptor activation. Lipid accumulation occurred in exposed worms. In conclusion, BPA, PPB, and TCS alter the physiology of growth, lipid accumulation, and reproduction in C. elegans, most likely through oxidative stress mechanisms.
Keyphrases
- heat shock protein
- heat shock
- heat stress
- oxidative stress
- reactive oxygen species
- wild type
- healthcare
- escherichia coli
- genome wide
- magnetic resonance
- magnetic resonance imaging
- fatty acid
- quantum dots
- gene expression
- binding protein
- single molecule
- quality improvement
- small molecule
- living cells
- pain management
- diabetic rats
- computed tomography
- ischemia reperfusion injury
- chronic pain
- transcription factor
- amino acid
- health insurance
- fluorescent probe
- ionic liquid