TY - JOUR
T1 - Embryonic exposure to tetrabromobisphenol A and its metabolites, bisphenol A and tetrabromobisphenol A dimethyl ether disrupts normal zebrafish (Danio rerio) development and matrix metalloproteinase expression
AU - Mccormick, Jessica M.
AU - Paiva, Michael S.
AU - Häggblom, Max M.
AU - Cooper, Keith R.
AU - White, Lori A.
N1 - Funding Information:
This work was supported by the Hudson River Foundation, the New Jersey Agricultural Experimental Station, the National Institute for Environmental Health and Safety Center Grant (ES05022), and the Department of Defense/SERDP (ER-1492).
PY - 2010/11/1
Y1 - 2010/11/1
N2 - Tetrabromobisphenol A (TBBPA) is a widely used brominated flame retardant that is persistent in the environment and detected in human serum and breast milk. TBBPA is microbiologically transformed in anaerobic environments to bisphenol A (BPA) and in aerobic environments to TBBPA dimethyl ether (TBBPA DME). Despite the detection of TBBPA DME in the environment, the resulting toxicity is not known. The relative toxicity of TBBPA, BPA and TBBPA DME was determined using embryonic exposure of zebrafish, with BPA and TBBPA DME exhibiting lower potency than TBBPA. TBBPA exposure resulted in 100% mortality at 3 (1.6. mg/L) and 1.5 μM (0.8. mg/L), whereas BPA and TBBPA DME did not result in significant embryonic mortality in comparison to controls. While all three caused edema and hemorrhage, only TBBPA specifically caused decreased heart rate, edema of the trunk, and tail malformations. Matrix metalloproteinase (MMP) expression was measured due to the role of these enzymes in the remodeling of the extracellular matrix during tissue morphogenesis, wound healing and cell migration. MMP-2, -9 and -13 expression increased (2-8-fold) after TBBPA exposure followed by an increase in the degradation of collagen I and gelatin. TBBPA DME exposure resulted in only a slight increase (less than 2-fold) in MMP expression and did not significantly increase enzymatic activity. These data suggest that TBBPA is more potent than BPA or TBBPA DME and indicate that the trunk and tail phenotypes seen after TBBPA exposure could be due in part to alteration of proper MMP expression and activity.
AB - Tetrabromobisphenol A (TBBPA) is a widely used brominated flame retardant that is persistent in the environment and detected in human serum and breast milk. TBBPA is microbiologically transformed in anaerobic environments to bisphenol A (BPA) and in aerobic environments to TBBPA dimethyl ether (TBBPA DME). Despite the detection of TBBPA DME in the environment, the resulting toxicity is not known. The relative toxicity of TBBPA, BPA and TBBPA DME was determined using embryonic exposure of zebrafish, with BPA and TBBPA DME exhibiting lower potency than TBBPA. TBBPA exposure resulted in 100% mortality at 3 (1.6. mg/L) and 1.5 μM (0.8. mg/L), whereas BPA and TBBPA DME did not result in significant embryonic mortality in comparison to controls. While all three caused edema and hemorrhage, only TBBPA specifically caused decreased heart rate, edema of the trunk, and tail malformations. Matrix metalloproteinase (MMP) expression was measured due to the role of these enzymes in the remodeling of the extracellular matrix during tissue morphogenesis, wound healing and cell migration. MMP-2, -9 and -13 expression increased (2-8-fold) after TBBPA exposure followed by an increase in the degradation of collagen I and gelatin. TBBPA DME exposure resulted in only a slight increase (less than 2-fold) in MMP expression and did not significantly increase enzymatic activity. These data suggest that TBBPA is more potent than BPA or TBBPA DME and indicate that the trunk and tail phenotypes seen after TBBPA exposure could be due in part to alteration of proper MMP expression and activity.
KW - Bisphenol A
KW - Brominated flame retardant
KW - Matrix metalloproteinases
KW - Tetrabromobisphenol A
KW - Tetrabromobisphenol A dimethyl ether
KW - Zebrafish
UR - http://www.scopus.com/inward/record.url?scp=78449281873&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78449281873&partnerID=8YFLogxK
U2 - 10.1016/j.aquatox.2010.07.019
DO - 10.1016/j.aquatox.2010.07.019
M3 - Article
C2 - 20728951
AN - SCOPUS:78449281873
VL - 100
SP - 255
EP - 262
JO - Aquatic Toxicology
JF - Aquatic Toxicology
SN - 0166-445X
IS - 3
ER -