دانلود مقاله ISI انگلیسی شماره 76231
ترجمه فارسی عنوان مقاله

اثرات استرس بارداری و درمان ضد افسردگی مهارکننده بازجذب سروتونین انتخابی بر انعطاف پذیری ساختاری در مغز پس از زایمان - مدل ترجمه برای افسردگی پس از زایمان

عنوان انگلیسی
The effects of gestational stress and Selective Serotonin reuptake inhibitor antidepressant treatment on structural plasticity in the postpartum brain — A translational model for postpartum depression
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
76231 2016 8 صفحه PDF
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Hormones and Behavior, Volume 77, January 2016, Pages 124–131

ترجمه کلمات کلیدی
آمیگدال؛ برآمدگی دندریتیک؛ مادر؛ حالت؛ نوکلئوس اکومبنس؛ قشر جلوی مغز
کلمات کلیدی انگلیسی
Amygdala; Dendritic spines; Maternal; Mood; Nucleus accumbens; Prefrontal cortex

چکیده انگلیسی

Postpartum depression (PPD) is a common complication following childbirth experienced by one in every five new mothers. Although the neural basis of PPD remains unknown, previous research in rats has shown that gestational stress, a risk factor for PPD, induces depressive-like behavior during the postpartum period. Moreover, the effect of gestational stress on postpartum mood is accompanied by structural modifications within the nucleus accumbens (NAc) and the medial prefrontal cortex (mPFC)–limbic regions that have been linked to PPD. Mothers diagnosed with PPD are often prescribed selective serotonin reuptake inhibitor (SSRI) antidepressant medications and yet little is known about their effects in models of PPD. Thus, here we investigated whether postpartum administration of Citalopram, an SSRI commonly used to treat PPD, would ameliorate the behavioral and morphological consequences of gestational stress. In addition, we examined the effects of gestational stress and postpartum administration of Citalopram on structural plasticity within the basolateral amygdala (BLA) which together with the mPFC and NAc forms a circuit that is sensitive to stress and is involved in mood regulation. Our results show that postpartum rats treated with Citalopram do not exhibit gestational stress-induced depressive-like behavior in the forced swim test. In addition, Citalopram was effective in reversing gestational stress-induced structural alterations in the postpartum NAc shell and mPFC. We also found that gestational stress increased spine density within the postpartum BLA, an effect which was not reversed by Citalopram treatment. Overall, these data highlight the usefulness of gestational stress as a valid and informative translational model for PPD. Furthermore, they suggest that structural alterations in the mPFC–NAc pathway may underlie stress-induced depressive-like behavior during the postpartum period and provide much needed information on how SSRIs may act in the maternal brain to treat PPD.