کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6257607 1612954 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research reportCortisol responses to chronic stress in adult macaques: Moderation by a polymorphism in the serotonin transporter gene
ترجمه فارسی عنوان
تحقیقات انجام شده پاسخ کورتیزول به استرس مزمن در میکروسکوپ بزرگسالان: مدیریت با چندشکلی در ژن انتقال دهنده سروتونین
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
چکیده انگلیسی


- Rh5-HTTLPR exerted an influence on cortisol responses to stress in macaques.
- The s/s genotype was associated with increased cortisol responses to stress.
- In the absence of stress, no differences related to genotype were observed.
- This moderation was a genetic modulation of cortisol responses to stress.

Accumulating evidence has shown that a polymorphism in the promoter region of the serotonin transporter gene (5-HTTLPR) moderates the association between stress and depressive symptoms. However, the exact etiologies underlying this moderation are not well understood. Here it is reported that among adult female rhesus macaques, an orthologous polymorphism (rh5-HTTLPR) exerted an influence on cortisol responses to chronic stress. It was found that females with two copies of the short allele were associated with increased cortisol responses to chronic stress in comparison to their counterparts who have one or two copies of the long allele. In the absence of stress, no differences related to genotype were observed in these females. This genetic moderation was found without a genetic influence on exposure to stressful situations. Rather it was found to be a genetic modulation of cortisol responses to chronic stress. These findings indicate that the rh5-HTTLPR polymorphism is closely related to hypothalamus-pituitary-adrenal (HPA) axis reactivity, which may increase susceptibility to depression in females with low serotonin transporter efficiency and a history of stress.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Behavioural Brain Research - Volume 278, 1 February 2015, Pages 280-285
نویسندگان
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