RESUMO
In this study, we investigate the effect of sexual assault on sexual function in adult women. Participants consisted of 136 women recruited from the Emergency Clinic for Rape Victims in Stockholm. Seventy-three women returned for follow-up six months after the assault and completed the Female Sexual Function Index, assessing their current sexual function compared to that before the assault. A majority (44/73) reported impaired function, which was associated with a simultaneous diagnosis of PTSD (OR 5.7; 95% CI 1.7-19.1, p = .005) or moderate-severe depressive symptoms (OR 4.6; 95% CI 1.6-13.7, p = .006). 27% of women reported improved function.
Assuntos
Vítimas de Crime , Estupro , Delitos Sexuais , Transtornos de Estresse Pós-Traumáticos , Adulto , Feminino , Humanos , Fatores de Risco , Transtornos de Estresse Pós-Traumáticos/epidemiologiaRESUMO
Nogo receptor 1 (NgR1) is expressed in forebrain neurons and mediates nerve growth inhibition in response to Nogo and other ligands. Neuronal activity downregulates NgR1 and the inability to downregulate NgR1 impairs long-term memory. We investigated behavior in a serial behavioral paradigm in mice that overexpress or lack NgR1, finding impaired locomotor behavior and recognition memory in mice lacking NgR1 and impaired sequential spatial learning in NgR1 overexpressing mice. We also investigated a role for NgR1 in drug-mediated sensitization and found that repeated cocaine exposure caused stronger locomotor responses but limited development of stereotypies in NgR1 overexpressing mice. This suggests that NgR1-regulated synaptic plasticity is needed to develop stereotypies. Ex vivo magnetic resonance imaging and diffusion tensor imaging analyses of NgR1 overexpressing brains did not reveal any major alterations. NgR1 overexpression resulted in significantly reduced density of mature spines and dendritic complexity. NgR1 overexpression also altered cocaine-induced effects on spine plasticity. Our results show that NgR1 is a negative regulator of both structural synaptic plasticity and dendritic complexity in a brain region-specific manner, and highlight anterior cingulate cortex as a key area for memory-related plasticity.