Bioaccumulation and biochemical effects of ethylhexyl methoxy cinnamate and its main transformation products in zebrash
- 1. Key Laboratory for Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, Nanjing 210098 (China)
- 2. Water Conservancy Project & Civil Engineering College, Tibet Agriculture & Animal Husbandry University, Linzhi 860000 (China)
Description
Highlights: • Both EHMC and its transformation products accumulated in zebrafish. • 3,5DCl2HAcP was the main accumulated transformation product of EHMC in zebrafish. • 3,5DCl2HAcP induced estrogen and androgen effects on zebrafish different from EHMC. • 3,5DCl2HAcP altered the sex hormone interference effects caused by EHMC. • Both EHMC and 3,5DCl2HAcP caused oxidative damage in zebrafish. -- Abstract: The purpose of this study was to investigate the bioaccumulation and biochemical responses exposed to one of the main organic ultraviolet (UV) pollutants in the environment, ethylhexyl methoxy cinnamate (EHMC), and its main transformation product, either alone or in combination in zebrash (Danio rerio). Four-month-old zebrafish were exposed to EHMC (34.4, 344 nmol/L) solution for 14 days, the species and contents of EHMC transformation products in zebrafish were determined and 3,5-dichloro-2-hydroxyacetophenone (3,5DCl2HAcP) was the one with the highest concentration in transformation products. Then, zebrafish were exposed to EHMC, 3,5DCl2HAcP alone and mixed solution for 21 days. At 7, 14 and 21 d, the related indexes of antioxidant defense system were determined. Results showed that both EHMC and 3,5DCl2HAcP can lead to the increase of malondialdehyde (MDA) and glutathione (GSH) contents, superoxide dismutase (SOD), catalase (CAT) and glutathione reductase (GR) activities in visceral mass compared with the corresponding control group, thus produced oxidative stress effect in organism and 3,5DCl2HAcP even showed stronger oxidative stress than EHMC. The effects of the two lower concentration co-exposure groups were similar and more significant to that of single exposure groups, while excessive oxidative stress occurred at the highest co-exposure group indicated by the decrease of GSH content, SOD, CAT, GR activities and the continued increase of MDA content. At 21 d, estradiol (E2), vitellogenin (Vtg) and testosterone (T) contents, estrogen receptor (Esr), progesterone receptor (Pgr), androgen receptor (Ar), Vtg1, P450 aromatase (Cyp19a1) and 17β-hydroxysteroid dehydrogenase (Hsd17b3) expression were all significantly increased when exposed to 3,5DCl2HAcP alone, showing complex estrogen and androgen effects. When exposed to EHMC alone, E2 and Vtg contents, Esr, Pgr, Vtg1, Cyp19a1 and Hsd17b1 gene expression levels decreased significantly, and T content and Ar and Hsd17b3 expression increased significantly, indicated that EHMC can produce anti-estrogen and androgen effect. Last, the decrease of estrogen effect and increase of androgen effect in co-exposure group suggested that 3,5DCl2HAcP might weaken the estrogen effect and promote the androgen effect of EHMC.
Additional details
Identifiers
- DOI
- 10.1016/j.aquatox.2019.105241;
- PII
- S0166445X19304151;
Publishing Information
- Journal Title
- Aquatic Toxicology
- Journal Volume
- 214
- Journal Page Range
- vp.
- ISSN
- 0166-445X
- CODEN
- AQTODG
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55044303
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ANTIOXIDANTS; BIOLOGICAL ACCUMULATION; CATALASE; ECOLOGICAL CONCENTRATION; ESTRADIOL; GLUTATHIONE; OXIDATION; POLLUTANTS; PROGESTERONE; RECEPTORS; SUPEROXIDE DISMUTASE; TESTOSTERONE; ULTRAVIOLET RADIATION
- Descriptors DEC
- ANDROGENS; ANDROSTANES; CHEMICAL REACTIONS; DRUGS; ELECTROMAGNETIC RADIATION; ENZYMES; ESTRANES; ESTROGENS; HORMONES; HYDROXY COMPOUNDS; KETONES; MEMBRANE PROTEINS; ORGANIC COMPOUNDS; OXIDOREDUCTASES; PEPTIDES; PEROXIDASES; POLYPEPTIDES; PREGNANES; PROTEINS; RADIATIONS; RADIOPROTECTIVE SUBSTANCES; RESPONSE MODIFYING FACTORS; STEROID HORMONES; STEROIDS
Optional Information
- Copyright
- Copyright (c) 2019 Elsevier B.V. All rights reserved.