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Embryonic toxicity of 3,4-dichloroaniline (3,4-DCA) on Javanese medaka ( Bleeker, 1854). | LitMetric

AI Article Synopsis

  • Early exposure to toxic chemicals like 3,4-Dichloroaniline (3,4-DCA) can lead to lasting physiological and morphological changes, as shown in a study on Javanese medaka embryos.
  • Acute toxicity tests identified a median lethal concentration of 32.87 mg/L for 96 hours, while sublethal exposure (0.10 to 5.00 mg/L) revealed significant changes in heart rate at specific concentrations over time.
  • The findings suggest that while Javanese medaka embryos are relatively resistant to acute toxicity, they still experience harmful developmental effects at lower, sublethal concentrations.

Article Abstract

Early-life exposure to toxic chemicals causes irreversible morphological and physiological abnormalities that may last for a lifetime. The present study aimed to determine the toxicity effect of 3,4-Dichloroaniline (3,4-DCA) on Javanese medaka () embryos. Healthy embryos were exposed to various 3,4-DCA concentrations for acute toxicity (5, 10, 25, 50, and 100 mg.L) and sublethal toxicity (0.10, 0.50, 1.25, 2.50, and 5.00 mg.L) for 96 h and 20 days respectively. Acute toxicity test revealed that the median lethal concentration (96h-LC) was 32.87 mg.L (95 % CI = 27.90-38.74, R = 0.95). Sublethal exposure revealed that 1.25 mg.L at 3 days post-exposure (3 dpe) has a significant lower heartrate (120 ± 12.3 beats/min., p < 0.01), while at 7 dpe those exposed to 5 mg.L (141.8 ± 8.3 beats/min) had significantly (p < 0.01) lower heart rate compared to other treatments. Likewise, at 13 dpe, 5.00 mg.L (110.4 ± 17.3 beats/min) and 2.5 mg.L (130.4 ± 8.3 beats/min) were significantly lower (p < 0.001) compared to control. None of the embryos in 5.00 mg.L and 2.50 mg.L treatment groups survived at the end of the experiment. The results indicated a concentration-dependent response. The lowest observed effect concentration (LOEC) that exerted developmental deformities was 0.5 mg.L. Javanese medaka embryo have low sensitivity to acute toxicity of 3,4-DCA, but developmental abnormalities at sublethal concentrations were observed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472802PMC
http://dx.doi.org/10.1016/j.toxrep.2020.08.011DOI Listing

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