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Male and female variability in response to chronic stress and morphine in C57BL/6J, DBA/2J, and their BXD progeny

Carole MoreliD, Lyonna F. PariseiD, Yentl Y. van der ZeeiD, Orna IssleriD, Min CaiiD, Caleb J. BrowneiD, Anthony Blando, Katherine B. LeClairiD, Sherod E. HaynesiD, Robert W. WilliamsiD, Megan K. MulliganiD, Scott J. RussoiD, Eric J. NestleriD, Ming‐Hu HaniD

Abstract

Drug addiction is a multifactorial syndrome in which genetic predispositions and exposure to environmental stressors constitute major risk factors for the early onset, escalation, and relapse of addictive behaviors. While it is well known that stress plays a key role in drug addiction, the genetic factors that make certain individuals particularly sensitive to stress and thereby more vulnerable to becoming addicted are unknown. In an effort to test a complex set of gene x environment interactions--specifically gene x chronic stress--here we leveraged a systems genetics resource: BXD recombinant inbred mice (BXD5, BXD8, BXD14, BXD22, BXD29, and BXD32) and their parental mouse lines, C57BL/6J and DBA/2J. Utilizing the chronic social defeat stress (CSDS) and chronic variable stress (CVS) paradigms, we first showed sexual dimorphism in the behavioral stress response between the mouse strains. Further, we observed an interaction between genetic background and vulnerability to prolonged exposure to non-social stressors. Finally, we found that DBA/2J and C57BL/6J mice pre-exposed to stress displayed differences in morphine sensitivity. Our results support the hypothesis that genetic variation in predisposition to stress responses influences morphine sensitivity and is likely to modulate the development of drug addiction.

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02 /Specification & Classification

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