Involvement of COX2–thromboxane pathway in TCDD-induced precardiac edema in developing zebrafish
Creators
- 1. School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu (Japan)
- 2. School of Pharmacy, University of Wisconsin, Madison, WI (United States)
- 3. Biology Department, Woods Hole Oceanographic Institution, Woods Hole, MA (United States)
Description
Highlights: • We establish a new indicator of pericardial edema in developing zebrafish (precardiac edema). • Property of precardiac edema by TCDD is similar to that for conventional pericardial edema. • COX2b (but not COX2a)–thromboxane pathway is involved in precardiac edema by TCDD. - Abstract: The cardiovascular system is one of the most characteristic and important targets for developmental toxicity by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in fish larvae. However, knowledge of the mechanism of TCDD-induced edema after heterodimerization of aryl hydrocarbon receptor type 2 (AHR2) and AHR nuclear translocator type 1 (ARNT1) is still limited. In the present study, microscopic analysis with a high-speed camera revealed that TCDD increased the size of a small cavity between the heart and body wall in early eleutheroembryos, a toxic effect that we designate as precardiac edema. A concentration–response curve for precardiac edema at 2 days post fertilization (dpf) showed close similarity to that for conventional pericardial edema at 3 dpf. Precardiac edema caused by TCDD was reduced by morpholino knockdown of AHR2 and ARNT1, as well as by an antioxidant (ascorbic acid). A selective inhibitor of cyclooxygenase type 2 (COX2), NS398, also markedly inhibited TCDD-induced precardiac edema. A thromboxane receptor (TP) antagonist, ICI-192,605 almost abolished TCDD-induced precardiac edema and this effect was canceled by U46619, a TP agonist, which was not influential in the action of TCDD by itself. Knockdown of COX2b and thromboxane A synthase 1 (TBXS), but not COX2a, strongly reduced TCDD-induced precardiac edema. Knockdown of COX2b was without effect on mesencephalic circulation failure caused by TCDD. The edema by TCDD was also inhibited by knockdown of c-mpl, a thrombopoietin receptor necessary for thromobocyte production. Finally, induction of COX2b, but not COX2a, by TCDD was seen in eleutheroembryos at 3 dpf. These results suggest a role of the COX2b–thromboxane pathway in precardiac edema formation following TCDD exposure in developing zebrafish
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aquatox.2014.04.025Additional details
Identifiers
- DOI
- 10.1016/j.aquatox.2014.04.025;
- PII
- S0166-445X(14)00154-4;
Publishing Information
- Journal Title
- Aquatic Toxicology
- Journal Volume
- 154
- Journal Page Range
- p. 19-26
- ISSN
- 0166-445X
- CODEN
- AQTODG
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47016102
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ABUNDANCE; ANTIOXIDANTS; ASCORBIC ACID; CONCENTRATION RATIO; DIOXIN; ECOLOGICAL CONCENTRATION; EDEMA; FERTILIZATION; HEART; HYDROCARBONS; INDUCTION; LARVAE; MAXIMUM PERMISSIBLE LEVEL; RECEPTORS; TOXICITY; VELOCITY; WALLS
- Descriptors DEC
- BODY; CARDIOVASCULAR SYSTEM; DIMENSIONLESS NUMBERS; HETEROCYCLIC COMPOUNDS; MEMBRANE PROTEINS; ORGANIC COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANS; PATHOLOGICAL CHANGES; PROTEINS; SAFETY STANDARDS; STANDARDS; SYMPTOMS; VITAMINS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.