TitleEthanol-dependent toxicity in zebrafish is partially attenuated by antioxidants.
Publication TypeJournal Article
Year of Publication2006
AuthorsReimers, MJ, La Du, JK, Pereira, CB, Giovanini, J, Tanguay, RL
JournalNeurotoxicol Teratol
Volume28
Issue4
Pagination497-508
Date Published2006 Jul-Aug
ISSN0892-0362
KeywordsAnimals, Antioxidants, Apoptosis, Cell Death, Central Nervous System Depressants, Dose-Response Relationship, Drug, Edema, Embryo, Nonmammalian, Embryonic Development, Ethanol, In Situ Nick-End Labeling, Oxidative Stress, Pericardium, Zebrafish
Abstract

Ethanol is a well-established developmental toxicant; however, the molecular and cellular mechanism(s) of toxicity remains unclear. It has been suggested that ethanol metabolism leads to oxidative stress resulting in an increase in cell death. Alcohol developmental toxicity has not been well studied in zebrafish; however, zebrafish represent an excellent vertebrate model for investigating and understanding normal and aberrant development. To evaluate ethanol metabolism dependent toxicity, chemical inhibitors of the ethanol metabolizing enzymes were utilized. Embryos co-exposed to ethanol and a combination of ethanol metabolism inhibitors led to a significant increase in the occurrence of pericardial edema. Further, in the presence of the inhibitor mixture there was an increase in developmental malformations at lower ethanol concentrations. Cell death has been implicated as a potential explanation for ethanol-dependent toxicity. Using cell death assays, ethanol significantly increased embryonic cell death. To determine if oxidative stress underlies cardiovascular dysfunction, embryos were co-exposed to ethanol and several antioxidants. The antioxidants, glutathione and lipoic acid, partially attenuated the incidence of pericardial edema. The effectiveness of the antioxidants to protect the embryos from ethanol-induced cell death was also evaluated. The antioxidants provided no protection against cell death. Thus, ethanol-mediated pericardial edema and cell death appear to be mechanistically distinct.

DOI10.1016/j.ntt.2006.05.007
Alternate JournalNeurotoxicol Teratol
PubMed ID16904866
Grant ListES00210 / ES / NIEHS NIH HHS / United States
R21 AA012783 / AA / NIAAA NIH HHS / United States
ES03850 / ES / NIEHS NIH HHS / United States
AA12783 / AA / NIAAA NIH HHS / United States
P30 ES000210 / ES / NIEHS NIH HHS / United States