PUBLICATION

Venlafaxine deposition in the zygote disrupts the endocrine control of growth in juvenile zebrafish

Authors
Thompson, W.A., Vijayan, M.M.
ID
ZDB-PUB-210714-19
Date
2021
Source
Environmental research   202: 111665 (Journal)
Registered Authors
Vijayan, Mathilakath
Keywords
Antidepressants, Endocrine disruption, Feeding, GH-IGF axis, Glucocorticoids, Insulin, Municipal wastewater effluent, Pharmaceuticals
MeSH Terms
  • Animals
  • Larva
  • Venlafaxine Hydrochloride/toxicity
  • Water Pollutants, Chemical*/toxicity
  • Zebrafish*
  • Zygote
PubMed
34252433 Full text @ Environ. Res.
Abstract
The antidepressant venlafaxine can be found at levels nearing μg/L in waterways receiving municipal wastewater effluent, exposing non-target organisms, such as fish, to this chemical. We showed previously that zygotic exposure to venlafaxine alters neurodevelopment and behaviour in zebrafish (Danio rerio) larvae. Here, we tested the hypothesis that the zygotic deposition of venlafaxine disrupts endocrine pathways related to growth in zebrafish. This was carried out by microinjecting embryos (1-4 cell stage) with either 0, 1, or 10 ng venlafaxine. Zygotic venlafaxine deposition reduced the growth of fish after 30 days post-fertilization. Specific growth rate was particularly impacted by 1 ng venlafaxine. This growth retardation corresponded with the disruption of endocrine pathways involved in growth and metabolism. Venlafaxine exposed embryos displayed reduced transcript abundance of key genes involved in anabolic hormone action. Early-life venlafaxine exposure also reduced whole-body insulin and glucose content in juveniles. Target-tissue glucose uptake measurements indicated that high venlafaxine deposition preferentially increased glucose uptake to the brain. Zygotic venlafaxine did not affect feed intake nor altered the transcript abundance of key feeding-related peptides. Taken together, zygotic venlafaxine deposition compromises zebrafish growth by disrupting multiple endocrine pathways, and this study has identified key markers for potential use in risk assessment.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping