Sex differences in anxiety and emotional behavior

• Published in: Pflügers Archiv 2013-05, Vol.465 (5), p.601-626
• Main Authors: Donner, Nina C., Lowry, Christopher A.
• Format: Article
• Language: English
• Subjects: Animals; Anxiety; Anxiety - metabolism; Anxiety - physiopathology; Biomedical and Life Sciences; Biomedicine; Cell Biology; Female; Human Physiology; Humans; Invited Review; Male; Molecular Medicine; Neurosciences; Panic Disorder - metabolism; Panic Disorder - physiopathology; Receptors; Rodentia; Sex Characteristics; Stress Disorders, Post-Traumatic - metabolism; Stress Disorders, Post-Traumatic - physiopathology
• ISSN: 0031-6768; 1432-2013
• DOI: 10.1007/s00424-013-1271-7

Research has elucidated causal links between stress exposure and the development of anxiety disorders, but due to the limited use of female or sex-comparative animal models, little is known about the mechanisms underlying sex differences in those disorders. This is despite an overwhelming wealth of evidence from the clinical literature that the prevalence of anxiety disorders is about twice as high in women compared to men, in addition to gender differences in severity and treatment efficacy. We here review human gender differences in generalized anxiety disorder, panic disorder, posttraumatic stress disorder and anxiety-relevant biological functions, discuss the limitations of classic conflict anxiety tests to measure naturally occurring sex differences in anxiety-like behaviors, describe sex-dependent manifestation of anxiety states after gestational, neonatal, or adolescent stressors, and present animal models of chronic anxiety states induced by acute or chronic stressors during adulthood. Potential mechanisms underlying sex differences in stress-related anxiety states include emerging evidence supporting the existence of two anatomically and functionally distinct serotonergic circuits that are related to the modulation of conflict anxiety and panic-like anxiety, respectively. We discuss how these serotonergic circuits may be controlled by reproductive steroid hormone-dependent modulation of crfr1 and crfr2 expression in the midbrain dorsal raphe nucleus and by estrous stage-dependent alterations of γ-aminobutyric acid (GABAergic) neurotransmission in the periaqueductal gray, ultimately leading to sex differences in emotional behavior.