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Developmental toxicity from exposure to various forms of mercury compounds in medaka fish (Oryzias latipes) embryos.
Abstract
This study examined developmental toxicity of different mercury compounds, including
some used in traditional medicines. Medaka (Oryzias latipes) embryos were exposed
to 0.001-10 µM concentrations of MeHg, HgCl2, α-HgS (Zhu Sha), and β-HgS (Zuotai)
from stage 10 (6-7 hpf) to 10 days post fertilization (dpf). Of the forms of mercury
in this study, the organic form (MeHg) proved the most toxic followed by inorganic
mercury (HgCl2), both producing embryo developmental toxicity. Altered phenotypes
included pericardial edema with elongated or tube heart, reduction of eye pigmentation,
and failure of swim bladder inflation. Both α-HgS and β-HgS were less toxic than MeHg
and HgCl2. Total RNA was extracted from survivors three days after exposure to MeHg
(0.1 µM), HgCl2 (1 µM), α-HgS (10 µM), or β-HgS (10 µM) to examine toxicity-related
gene expression. MeHg and HgCl2 markedly induced metallothionein (MT) and heme oxygenase-1
(Ho-1), while α-HgS and β-HgS failed to induce either gene. Chemical forms of mercury
compounds proved to be a major determinant in their developmental toxicity.
Type
Journal articleSubject
Developmental toxicityHeme oxygenase-1
HgCl2
MeHg
Medaka
Mercury
Metallothionein
α-HgS (Zhu Sha, cinnabar)
β-HgS (Zuotai)
Permalink
https://hdl.handle.net/10161/12720Published Version (Please cite this version)
10.7717/peerj.2282Publication Info
Dong, W; Liu, J; Wei, L; Jingfeng, Y; Chernick, M; & Hinton, DE (2016). Developmental toxicity from exposure to various forms of mercury compounds in medaka
fish (Oryzias latipes) embryos. PeerJ, 4. pp. e2282. 10.7717/peerj.2282. Retrieved from https://hdl.handle.net/10161/12720.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
David E. Hinton
Nicholas Distinguished Professor Emeritus of Environmental Quality
The Hinton laboratory focuses on mechanistic toxicity in all life stages of small,
aquarium model fish and in selected species with particular environmental relevance
(freshwater and marine). With the latter, investigations focus on stressor responses
and include follow up studies after oil spills. Studies with the laboratory model
fish take advantage of the compressed life cycle to improve understanding of organellar,
cellular and tissues responses that arise after exposure and follow either a

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