PUBLICATION

The case for thyroid disruption in early life stage exposures to thiram in zebrafish (Danio rerio)

Authors
Chen, X., Fang, M., Chernick, M., Wang, F., JingfengYang, ., Yu, Y., Zheng, N., Teraoka, H., Nanba, S., Hiraga, T., Hinton, D.E., Dong, W.
ID
ZDB-PUB-181109-10
Date
2018
Source
General and comparative endocrinology   271: 73-81 (Journal)
Registered Authors
Dong, Wu, Teraoka, Hiroki
Keywords
Acute exposure, Notochord, Thiram, Thyroid, Zebrafish
MeSH Terms
  • Animals
  • Bone Development/drug effects
  • Edema/pathology
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/metabolism
  • Gene Expression Regulation, Developmental/drug effects
  • Iodide Peroxidase/genetics
  • Iodide Peroxidase/metabolism
  • Larva/drug effects
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Thiram/toxicity*
  • Thyroid Gland/drug effects*
  • Zebrafish/anatomy & histology
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish/physiology*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed
30408483 Full text @ Gen. Comp. Endocrinol.
Abstract
Thiram, a pesticide in the dithiocarbamate chemical family, is widely used to prevent fungal disease in seeds and crops. Its off-site movement to surface waters occurs and may place aquatic organisms at potential harm. Zebrafish embryos were used for investigation of acute (1 h) thiram exposure (0.001-10 µM) at various developmental stages. Survival decreased at 1 µM and 10 µM and hatching was delayed at 0.1 µM and 1 µM. Notochord curvatures were seen at 0.1 and 1 μM thiram when exposure was initiated at 2 and at 10 hpf. Similar notochord curvatures followed exposure to the known TPO inhibitor, methimazole (MMI). Changes were absent in embryos exposed at later stages, i.e., 12 hpf. In embryos exposed to 0.1 or 1 μM at 10 hpf, levels of the thyroid enzyme, Deiodinase 3, increased by 12 hpf. Thyroid peroxide (TPO), important in T4 synthesis, decreased by 48 hpf in embryos exposed to 1 µM at 10 hpf. Thiram toxicity was stage-dependent and early life stage exposure may be responsible for adverse effects seen later. These effects may be due to impacts on the thyroid via regulation of specific thyroid genes including TPO and Deiodinase 3.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping