TY - JOUR
T1 - The molecular basis for sex differences in depression susceptibility
AU - Issler, Orna
AU - Nestler, Eric J.
N1 - Funding Information:
The review was prepared with support of the Hope for Depression Research Foundation (HDRF) and the National Institute of Mental Health. The authors thank Deena M Walker, Catherine J Pena and Erez Geron for fruitful discussions. Great thanks to Jill Gregory (Mount Sinai) for her illustrations.
Publisher Copyright:
© 2017
PY - 2018/10
Y1 - 2018/10
N2 - Depression is a prevalent, devastating psychiatric disorder which women are twice as likely to suffer as men. Yet, until recently, most of the mechanistic studies shedding light on the molecular pathways involved in depression have focused on males, both animals and humans. It has been established that women have a more sensitive stress response, and that sex hormones contribute to depression onset. Recent genome-wide studies on human and mouse brain tissue have revealed that the overlap in the genes regulated by depression or chronic stress, respectively, between the sexes is surprisingly low. Such unbiased comprehensive screening approaches combined with advanced bioinformatics and in vivo validation studies enable identifying truly novel target genes that contribute to sex differences in depression susceptibility. Furthermore, recent studies have demonstrated sex bias in transgenerational passage of the effects of stress to the offspring. Elucidating the sex-specific mechanisms contributing to the development of depression can help design better diagnostic and therapeutic tools aimed at normalizing the unique abnormalities of each gender.
AB - Depression is a prevalent, devastating psychiatric disorder which women are twice as likely to suffer as men. Yet, until recently, most of the mechanistic studies shedding light on the molecular pathways involved in depression have focused on males, both animals and humans. It has been established that women have a more sensitive stress response, and that sex hormones contribute to depression onset. Recent genome-wide studies on human and mouse brain tissue have revealed that the overlap in the genes regulated by depression or chronic stress, respectively, between the sexes is surprisingly low. Such unbiased comprehensive screening approaches combined with advanced bioinformatics and in vivo validation studies enable identifying truly novel target genes that contribute to sex differences in depression susceptibility. Furthermore, recent studies have demonstrated sex bias in transgenerational passage of the effects of stress to the offspring. Elucidating the sex-specific mechanisms contributing to the development of depression can help design better diagnostic and therapeutic tools aimed at normalizing the unique abnormalities of each gender.
UR - http://www.scopus.com/inward/record.url?scp=85040049587&partnerID=8YFLogxK
U2 - 10.1016/j.cobeha.2017.12.019
DO - 10.1016/j.cobeha.2017.12.019
M3 - Review article
AN - SCOPUS:85040049587
SN - 2352-1546
VL - 23
SP - 1
EP - 6
JO - Current Opinion in Behavioral Sciences
JF - Current Opinion in Behavioral Sciences
ER -