PUBLICATION

Developmental toxicity and neurotoxicity assessment of R-, S-, and RS-propylene glycol enantiomers in zebrafish (Danio rerio) larvae

Authors
Shen, C., Zhao, X., He, C., Zuo, Z.
ID
ZDB-PUB-220111-4
Date
2022
Source
Environmental science and pollution research international   29(20): 30537-30547 (Journal)
Registered Authors
He, Chengyong
Keywords
Danio rerio, Developmental toxicity, Enantiomers, Neurotoxicity, Propylene glycol
MeSH Terms
  • Animals
  • Embryo, Nonmammalian
  • Humans
  • Larva
  • Neurotoxicity Syndromes*
  • Propylene Glycol
  • Water Pollutants, Chemical*/toxicity
  • Zebrafish
PubMed
35000155 Full text @ Environ. Sci. Pollut. Res. Int.
Abstract
Propylene glycol (PG) is widely used in the foods, pharmaceuticals, oil industry, animal feed, cosmetics and other industries. Because of the existence of a chiral carbon center, PG forms R (Rectus)- and S (Sinister)-enantiomers. Currently, the toxicity study of its R-, S-enantiomers is still very scarce. In this study, we have assessed the developmental toxicity and neurotoxicity of the R-, S-, and RS-PG enantiomers in zebrafish larvae. We found that exposure to R-, S-, and RS-PG enantiomers did not significantly affect the basic developmental endpoints of embryos or larvae (i.e., embryonic movement, hatching, mortality, malformation, heartbeat, body length), indicating that R-, S-, and RS-PG exposures did not exhibit the basic developmental toxicity in zebrafish larvae. The toxicity of three enantiomers was lower than that of ethanol, and there was no significant difference between them. However, R-, S-, and RS-PG exposures with high doses could significantly change the eye diameter and locomotor activity of larval zebrafish, indicating that R-, S-, and RS-PG enantiomers of high doses could potentially exhibit the neurotoxicity and ocular developmental toxicity in zebrafish larvae. Therefore, the potential neurotoxicity and ocular developmental toxicity of R-, S-, and RS-PG enantiomers for infants and toddlers should be considered.
Genes / Markers
Figures
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Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping