苦恼
压力源
焦虑
心理学
医学
纤维肌痛
剧痛
应对(心理学)
压力(语言学)
痛阈
临床心理学
慢性疼痛
物理疗法
内科学
精神科
哲学
语言学
作者
Nirit Geva,Sari Golan,Lior Pinchas,Ruth Defrin
出处
期刊:Pain
[Ovid Technologies (Wolters Kluwer)]
日期:2022-08-09
卷期号:164 (3): 587-597
被引量:8
标识
DOI:10.1097/j.pain.0000000000002743
摘要
In Brief A reciprocity between the stress and the pain system is recognized; however, the manner by which sex affects this reciprocity is unclear. Understanding the interactions of stress, pain, and sex may shed light on the apparent women's vulnerability to chronic pain, which often coexists with increased distress, and to affective disorders, which often coexist with chronic pain. The study's aim was to examine the effect of acute, validated, psychosocial stress on pain perception and modulation of women and men in a controlled manner. Participants were 82 women and 66 men. Heat–pain threshold, heat–pain tolerance, and pain modulation by temporal summation of pain (TSP), and pain adaptation were measured before and after exposure to the Montreal Imaging Stress Task (MIST) or to a sham task. The stress response was verified by perceived ratings of stress and anxiety, autonomic variables, and salivary cortisol. A significant stress response was obtained by the MIST among both sexes; however, women displayed a greater increase in perceived distress, and men displayed a greater increase in cortisol. Among women, TSP decreased and pain adaptation increased following the MIST, responses that were predicted by perceived distress levels. Among men, TSP increased following the MIST but was not predicted by the stress variables. In conclusion, acute stress manipulation seems to differentially affect both stress and pain responses of women and men: women exhibited stress-induced antinociception and men exhibited stress-induced pronociception. Higher perceived stress levels among women may trigger a temporary increase in pain inhibition mechanisms to serve evolutionary purposes. Sex-specific pain responses under stress were observed in that women who exhibited an enhancement in pain inhibition capacity, whereas men exhibited an enhancement of pain excitability.
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