反安慰剂痛觉过敏、部分强化和消退。
Nocebo Hyperalgesia, Partial Reinforcement, and Extinction.
作者信息
Colagiuri Ben, Quinn Veronica F, Colloca Luana
机构信息
University of Sydney, School of Psychology, Sydney, Australia.
University of Sydney, School of Psychology, Sydney, Australia.
出版信息
J Pain. 2015 Oct;16(10):995-1004. doi: 10.1016/j.jpain.2015.06.012. Epub 2015 Jul 11.
UNLABELLED
Many studies have found evidence of conditioning-induced nocebo hyperalgesia. However, these studies have exclusively involved continuous reinforcement (CRF) schedules. Thus, it is currently unknown whether nocebo hyperalgesia can result after partial reinforcement (PRF). We tested this using electrodermal pain stimulation in healthy volunteers. Undergraduates (N = 135) received nocebo treatment under the guise of a hyperalgesic. Participants were randomly allocated to CRF, PRF, or control (no conditioning). Conditioning involved surreptitiously increasing pain stimulation on nocebo trials relative to control trials. During training, the CRF group always had the nocebo paired with the surreptitious pain increase, whereas the PRF group experienced the increase on only 62.5% of nocebo trials. In the test phase, pain stimulation was equivalent across nocebo and control trials. PRF was sufficient to induce nocebo hyperalgesia; however, this was weaker than CRF. Nocebo hyperalgesia failed to extinguish irrespective of the training schedule. Additional assessment of expectancies indicated strong concordance between expectancy and nocebo hyperalgesia. Overall, these findings suggest that once established, nocebo hyperalgesia may be difficult to disrupt. PRF may be a novel method of reducing the intensity of nocebo hyperalgesia in the clinic, which may be particularly important given its persistence.
PERSPECTIVE
This study provides novel evidence that partial reinforcement results in weaker nocebo hyperalgesia than continuous reinforcement and that nocebo hyperalgesia fails to extinguish, irrespective of the training schedule. As a result, partial reinforcement may serve as a method for reducing the intensity of nocebo hyperalgesia in the clinic.
未标注
许多研究已发现条件反射诱导的反安慰剂高敏反应的证据。然而,这些研究均只涉及连续强化(CRF)模式。因此,目前尚不清楚部分强化(PRF)后是否会产生反安慰剂高敏反应。我们在健康志愿者中使用皮肤电疼痛刺激对此进行了测试。本科生(N = 135)在一种高敏反应的幌子下接受反安慰剂治疗。参与者被随机分配到CRF、PRF或对照组(无条件反射)。条件反射包括在反安慰剂试验中相对于对照试验偷偷增加疼痛刺激。在训练期间,CRF组中反安慰剂总是与偷偷增加的疼痛配对,而PRF组仅在62.5%的反安慰剂试验中经历疼痛增加。在测试阶段,反安慰剂试验和对照试验中的疼痛刺激是等效的。PRF足以诱导反安慰剂高敏反应;然而,其比CRF诱导的反应弱。无论训练模式如何,反安慰剂高敏反应都不会消退。对预期的额外评估表明预期与反安慰剂高敏反应之间有很强的一致性。总体而言,这些发现表明,一旦形成,反安慰剂高敏反应可能难以消除。PRF可能是临床上降低反安慰剂高敏反应强度的一种新方法,鉴于其持续性,这可能尤为重要。
观点
这项研究提供了新的证据,表明部分强化导致的反安慰剂高敏反应比连续强化弱,且无论训练模式如何,反安慰剂高敏反应都不会消退。因此,部分强化可能是临床上降低反安慰剂高敏反应强度的一种方法。