Powers Mark B, Medina Johnna L, Burns Stephanie, Kauffman Brooke Y, Monfils Marie, Asmundson Gordon J G, Diamond Allison, McIntyre Christa, Smits Jasper A J
a Department of Psychology, Institute for Mental Health Research , The University of Texas at Austin , Austin , TX , USA.
Cogn Behav Ther. 2015;44(4):314-27. doi: 10.1080/16506073.2015.1012740. Epub 2015 Feb 23.
Brain-derived neurotrophic factor (BDNF) is associated with synaptic plasticity, which is crucial for long-term learning and memory. Some studies suggest that people suffering from anxiety disorders show reduced BDNF relative to healthy controls. Lower BDNF is associated with impaired learning, cognitive deficits, and poor exposure-based treatment outcomes. A series of studies with rats showed that exercise elevates BDNF and enhances fear extinction. However, this strategy has not been tested in humans. In this pilot study, we randomized participants (N = 9, 8 females, M(Age) = 34) with posttraumatic stress disorder (PTSD) to (a) prolonged exposure alone (PE) or (b) prolonged exposure+exercise (PE+E). Participants randomized to the PE+E condition completed a 30-minute bout of moderate-intensity treadmill exercise (70% of age-predicted HR(max)) prior to each PE session. Consistent with prediction, the PE+E group showed a greater improvement in PTSD symptoms (d = 2.65) and elevated BDNF (d = 1.08) relative to the PE only condition. This pilot study provides initial support for further investigation into exercise augmented exposure therapy.
脑源性神经营养因子(BDNF)与突触可塑性相关,而突触可塑性对长期学习和记忆至关重要。一些研究表明,与健康对照组相比,患有焦虑症的人BDNF水平降低。较低的BDNF与学习受损、认知缺陷以及基于暴露的治疗效果不佳有关。一系列对大鼠的研究表明,运动可提高BDNF水平并增强恐惧消退。然而,这一策略尚未在人类中进行测试。在这项初步研究中,我们将患有创伤后应激障碍(PTSD)的参与者(N = 9,8名女性,平均年龄 = 34岁)随机分为(a)单独延长暴露组(PE)或(b)延长暴露 + 运动组(PE + E)。随机分配到PE + E组的参与者在每次PE疗程之前完成30分钟的中等强度跑步机运动(年龄预测最大心率的70%)。与预测一致,相对于仅PE组,PE + E组在PTSD症状(d = 2.65)和BDNF升高(d = 1.08)方面有更大改善。这项初步研究为进一步研究运动增强暴露疗法提供了初步支持。