TY - JOUR
T1 - Aquatic toxicology of fluoxetine
T2 - Understanding the knowns and the unknowns
AU - Stewart, Adam Michael
AU - Grossman, Leah
AU - Nguyen, Michael
AU - Maximino, Caio
AU - Rosemberg, Denis Broock
AU - Echevarria, David J.
AU - Kalueff, Allan V.
N1 - Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2014/11/1
Y1 - 2014/11/1
N2 - Fluoxetine is one of the most prescribed psychotropic medications, and is an agent of increasing interest for environmental toxicology. Fish and other aquatic organisms are excellent models to study neuroactive small molecules like fluoxetine. However, prone to variance due to experimental factors, data obtained in these models need to be interpreted with caution, using proper experimental protocols, study designs, validated endpoints as well as well-established models and tests. Choosing the treatment protocol and dose range for fluoxetine and other serotonergic drugs is critical for obtaining valid test results and correct data interpretation. Here we discuss the value of aquatic models to study fluoxetine effects, based on prior high-quality research, and outline the directions of future translational studies in the field. We review fluoxetine-evoked phenotypes in acute vs. chronic protocols, discussing them in the contact of complex role of serotonin in behavioral regulation. We conclude that zebrafish and other aquatic models represent a useful in-vivo tool for fluoxetine pharmacology and (eco)toxicology research.
AB - Fluoxetine is one of the most prescribed psychotropic medications, and is an agent of increasing interest for environmental toxicology. Fish and other aquatic organisms are excellent models to study neuroactive small molecules like fluoxetine. However, prone to variance due to experimental factors, data obtained in these models need to be interpreted with caution, using proper experimental protocols, study designs, validated endpoints as well as well-established models and tests. Choosing the treatment protocol and dose range for fluoxetine and other serotonergic drugs is critical for obtaining valid test results and correct data interpretation. Here we discuss the value of aquatic models to study fluoxetine effects, based on prior high-quality research, and outline the directions of future translational studies in the field. We review fluoxetine-evoked phenotypes in acute vs. chronic protocols, discussing them in the contact of complex role of serotonin in behavioral regulation. We conclude that zebrafish and other aquatic models represent a useful in-vivo tool for fluoxetine pharmacology and (eco)toxicology research.
KW - Antidepressants
KW - Aquatic model
KW - Ecotoxicology
KW - Fluoxetine
KW - Neuroscience
KW - Zebrafish
UR - http://www.scopus.com/inward/record.url?scp=84908338194&partnerID=8YFLogxK
U2 - 10.1016/j.aquatox.2014.08.014
DO - 10.1016/j.aquatox.2014.08.014
M3 - Letter
C2 - 25245382
AN - SCOPUS:84908338194
SN - 0166-445X
VL - 156
SP - 269
EP - 273
JO - Aquatic Toxicology
JF - Aquatic Toxicology
ER -