Conditioned Pain Modulation in Sexual Assault Survivors

被引:9
|
作者
Hellman, Natalie [1 ]
Sturycz, Cassandra A. [1 ]
Lannon, Edward W. [1 ]
Kuhn, Bethany L. [1 ]
Guereca, Yvette M. [1 ]
Toledo, Tyler A. [1 ]
Payne, Michael F. [1 ]
Huber, Felicitas A. [1 ]
Demuth, Mara [1 ]
Palit, Shreela [1 ]
Shadlow, Joanna O. [1 ]
Rhudy, Jamie L. [1 ]
机构
[1] Univ Tulsa, Dept Psychol, 800 S Tucker Dr, Tulsa, OK 74104 USA
来源
JOURNAL OF PAIN | 2019年 / 20卷 / 09期
基金
美国国家科学基金会;
关键词
Conditioned pain modulation; sexual assault; nociceptive flexion reflex; trauma; pain; POSTTRAUMATIC-STRESS-DISORDER; NOXIOUS INHIBITORY CONTROLS; FLEXION REFLEX THRESHOLD; SPINAL NOCICEPTION; EMOTIONAL MODULATION; TEMPORAL SUMMATION; SUPRASPINAL MODULATION; LEARNED CONTROL; MECHANISMS; ANALGESIA;
D O I
10.1016/j.jpain.2019.02.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Sexual assault (SA) is associated with an increased risk of chronic pain, but the mechanisms for this relationship are poorly understood. To explore whether disrupted descending inhibition is involved, this study used a conditioned pain modulation task to study the inhibition of pain and the nociceptive flexion reflex (NFR; a correlate of spinal nociception) in 32 pain-free SA survivors. This group was compared with 32 pain-free, trauma-exposed persons without SA and a group of 40 pain-free persons who reported no trauma exposure. Conditioned pain modulation was assessed from painful electric stimulations (test stimulus) delivered to the ankle before, during, and after participants submerged their hand in painful 10 degrees C water (conditioning stimulus). Pain ratings and NFR were assessed in response to test stimuli. All groups demonstrated significant inhibition of pain during conditioned pain modulation. However, only the no trauma exposure group demonstrated significant inhibition of NFR. The persons without SA group showed no inhibition of NFR, whereas the SA group showed significant facilitation of the NFR. These findings suggest that trauma exposure may impair inhibitory cerebrospinal circuits, but that SA may specifically promote facilitation of spinal nociception. Perspective: This study suggests that trauma exposure disrupts the cerebrospinal inhibition of spinal nociception, but that exposure to SA further promotes chronic pain risk by facilitating spinal nociception. This finding help may help to elucidate the pain risk mechanisms in trauma survivors. (C) 2019 by the American Pain Society
引用
收藏
页码:1027 / 1039
页数:13
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