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首页> 外文期刊>Pain. >Cortisol affects pain sensitivity and pain-related emotional learning in experimental visceral but not somatic pain: a randomized controlled study in healthy men and women
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Cortisol affects pain sensitivity and pain-related emotional learning in experimental visceral but not somatic pain: a randomized controlled study in healthy men and women

机译:皮质醇在实验性内脏的疼痛敏感性和与疼痛相关的情感学习中,但不是躯体疼痛:健康男女随机对照研究

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摘要

Despite growing interest in the role of stress mediators in pain chronicity, the effects of the stress hormone Cortisol on acute pain remain incompletely understood. In a randomized, double-blind, placebo-controlled study with N = 100 healthy volunteers, we tested the effects of oral hydrocortisone (20 mg) in 2 widely used pain models for the visceral and somatic modality. Salivary Cortisol was increased in the hydrocortisone group (time x group: P < 0.001). For the visceral modality, assessed using pressure-controlled rectal distensions, hydrocortisone decreased the pain threshold from before to after treatment (time x group: P = 0.011), an effect primarily driven by women (time x sex: P = 0.027). For the somatic modality, cutaneous heat pain thresholds remained unaffected by hydrocortisone. Hydrocortisone did not alter perceived pain intensity or unpleasantness of either modality. Conditioned pain-related fear in response to predictive cues was only observed for the visceral modality (time x modality: P = 0.026), an effect that was significantly reduced by hydrocortisone compared with placebo (time x group: P = 0.028). This is the first psychopharmacological study to support that acutely increased Cortisol enhances pain sensitivity and impairs pain-related emotional learning within the visceral, but not the somatic pain modality. Stress-induced visceral hyperalgesia and deficits in emotional pain-related learning could play a role in the pathophysiology of chronic visceral pain.
机译:尽管对疼痛介质在疼痛慢性慢性的作用产生的兴趣,但应激激素皮质醇对急性疼痛的影响仍然不完全理解。在随机的双盲,安慰剂对照研究与N = 100个健康志愿者,我们测试了口腔和体细胞模型的2种广泛使用的疼痛模型中口服氢化可的松(20mg)的影响。氢化鞘酮基团(时间X组:P <0.001)增加唾液皮质醇。对于使用压力控制的直肠疏散评估的内脏态量,氢化可在治疗前将疼痛阈值降低(时间X组:P = 0.011),其主要由女性驱动(时间x性:P = 0.027)。对于躯体模态,皮肤热疼痛阈值仍未受到氢化可的来影响。氢化可源性没有改变任何形式的感知疼痛强度或令人不快的性。根据内脏模态观察到响应预测性提示的条件相关的恐惧(时间X模态:P = 0.026),与安慰剂相比,通过氢化胞蔻体显着降低的效果(时间x组:P = 0.028)。这是第一次支持皮质醇急性增加的精神医学研究,增强了疼痛敏感性,损害了内脏内的疼痛相关的情绪学习,但不是体细胞疼痛的方式。情绪痛苦相关的学习中应激诱导的内脏痛觉和缺陷可以在慢性内脏疼痛的病理生理学中发挥作用。

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