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Copper inhibits hatching of fish embryos via inducing reactive oxygen species and down-regulating Wnt signaling.

Authors :
Zhang, YanJun
Zhang, RuiTao
Sun, HaoJie
Chen, Qi
Yu, XueDong
Zhang, Ting
Yi, Ming
Liu, Jing-Xia
Source :
Aquatic Toxicology. Dec2018, Vol. 205, p156-164. 9p.
Publication Year :
2018

Abstract

Highlights • Cu2+ and CuNPs significantly suppressed hatching in a dosage-dependent manner. • ROS scavengers and Wnt signaling agonist significantly alleviated the suppression effects of Cu2+ and CuNPs on hatching. • Cu2+ and CuNPs delayed hatching via suppressing embryonic motility rather than stimulating hatching enzyme secretion. Abstract The copper ion (Cu2+) has been reported to suppress the hatching of fish. However, little is known about the underlying mechanism. In this study, copper nanoparticles (CuNPs) and Cu2+ were shown to significantly suppress hatching of zebrafish in a dosage-dependent manner, and reactive oxygen species (ROS) scavengers NAC (N -acetylcysteine) & GSH (reduced glutathione) and Wnt signaling agonist BIO (6-bromoindirubin-3′-oxime) significantly alleviated the suppressing effects of Cu2+ and CuNPs on egg hatching. Mechanistically, NAC, GSH, and BIO recovered the egg hatching in copper-treated group via increasing the embryonic motility rather than stimulating the expression and secretion of hatching enzymes before hatching. Additionally, no significant difference in egg hatching was observed between the control and Cu2+-treated group at 72 hpf (hours post fertilization) in cox17 mutant embryos, in which little ROS was producd after copper stimulation. This may be the first report that Cu2+ and CuNPs suppress embryonic motility and the subsequent hatching via inducing ROS and at the same time down-regulating Wnt signaling in fish embryos. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0166445X
Volume :
205
Database :
Academic Search Index
Journal :
Aquatic Toxicology
Publication Type :
Academic Journal
Accession number :
133044541
Full Text :
https://doi.org/10.1016/j.aquatox.2018.10.015