TY - JOUR
T1 - Lost in translation
T2 - how to upgrade fear memory research
AU - Flores, África
AU - Fullana, Miquel
AU - Soriano-Mas, Carles
AU - Andero, Raül
N1 - Funding Information:
Acknowledgements RA is supported by a NARSAD Young Investigator Grant #22434, Ramón y Cajal program RYC2014-15784, RETOS-MINECO SAF2016-76565-R and FEDER funds. MAF is supported by a PERIS contract from the Departament de Salud of Generalitat de (SLT002/16/00490). CSM is supported by a Miguel Servet contract from the Carlos III Health Institute (CPII16/00048). MAF and CSM are supported by grants (PI16/00144 and PI16/00889) from the Carlos III Health Institute and FEDER funds -a way to build Europe-. AF is supported by a Juan de la Cierva contract from the Spanish government's Economy and Competitiveness Ministry (FJCI-2016-29888). We would like to thank Nicole Gouws for proofreading the manuscript.
Publisher Copyright:
© 2017, Macmillan Publishers Limited, part of Springer Nature.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - We address some of the current limitations of translational research in fear memory and suggest alternatives that might help to overcome them. Appropriate fear responses are adaptive, but disruption of healthy fear memory circuits can lead to anxiety and fear-based disorders. Stress is one of the main environmental factors that can disrupt memory circuits and constitutes as a key factor in the etiopathology of these psychiatric conditions. Current therapies for anxiety and fear-based disorders have limited success rate, revealing a clear need for an improved understanding of their neurobiological basis. Although animal models are excellent for dissecting fear memory circuits and have driven tremendous advances in the field, translation of these findings into the clinic has been limited so far. Animal models of stress-induced pathological fear combined with powerful cutting-edge techniques would help to improve the translational value of preclinical studies. We also encourage combining animal and human research, including psychiatric patients in order to find new pharmacological targets with real therapeutic potential that will improve the extrapolation of the findings. Finally, we highlight novel neuroimaging approaches that improve our understanding of anxiety and fear-based disorders.
AB - We address some of the current limitations of translational research in fear memory and suggest alternatives that might help to overcome them. Appropriate fear responses are adaptive, but disruption of healthy fear memory circuits can lead to anxiety and fear-based disorders. Stress is one of the main environmental factors that can disrupt memory circuits and constitutes as a key factor in the etiopathology of these psychiatric conditions. Current therapies for anxiety and fear-based disorders have limited success rate, revealing a clear need for an improved understanding of their neurobiological basis. Although animal models are excellent for dissecting fear memory circuits and have driven tremendous advances in the field, translation of these findings into the clinic has been limited so far. Animal models of stress-induced pathological fear combined with powerful cutting-edge techniques would help to improve the translational value of preclinical studies. We also encourage combining animal and human research, including psychiatric patients in order to find new pharmacological targets with real therapeutic potential that will improve the extrapolation of the findings. Finally, we highlight novel neuroimaging approaches that improve our understanding of anxiety and fear-based disorders.
UR - http://www.scopus.com/inward/record.url?scp=85039984758&partnerID=8YFLogxK
U2 - 10.1038/s41380-017-0006-0
DO - 10.1038/s41380-017-0006-0
M3 - Review article
C2 - 29298989
SN - 1359-4184
VL - 23
SP - 2122
EP - 2132
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 11
ER -