Department of Structural and Functional Biology, University of Campinas, Rua Monteiro Lobato, 255, Cidade Universitaria Zeferino Vaz, Box 6109, Campinas, SP 13083-865, Brazil.
Department of Oral and Maxillofacial Surgery, University of California San Francisco, 513 Parnassus Ave, Box 0440 S709, San Francisco, CA 94143, United States of America.
J Affect Disord. 2020 Sep 1;274:759-767. doi: 10.1016/j.jad.2020.05.144. Epub 2020 May 31.
There is great comorbidity and similarity between chronic pain and major depressive disorders. We have recently shown that 10 days of social defeat stress (SDS) induces hyperalgesia regardless depressive-like behavior in mice. Here we aimed to investigate whether social stress predisposes to chronic pain and, inversely, whether chronic pain predisposes to stress-induced depression.
Firstly, we used the 10 days SDS paradigm in mice followed by a mild protocol of repetitive inflammatory stimulus to evaluate if SDS would predispose to persistent hyperalgesia development. Secondly, we used the intense protocol of repetitive inflammatory stimulus followed by a subthreshold SDS to evaluate if persistent hyperalgesia would predispose to depressive-like behavior of social avoidance.
Our results showed that SDS predispose to chronic pain, since stressed mice injected with PGE2 for 7 days (mild protocol), stimuli normally not sufficient to trigger chronic pain, showed persistent hyperalgesia. Also, we showed that persistent hyperalgesia induced by repetitive inflammatory stimuli predispose to long-lasting depressive-like behavior of social avoidance induced by subthreshold SDS.
We did not analyze molecular mechanism associated with chronic pain and depressive-like behavior induced by SDS. However, we hypothesized that SDS and 14 days of PGE2 would generate neuroplasticity on brain areas shared by chronic pain and depression, predisposing to pain chronification and depressive-like behavior, respectively.
We can conclude social stress as a key and a common factor for chronic pain and depression. We can also conclude that SDS predisposes to chronic pain and, inversely, chronic pain predisposes to depressive-like behavior.
慢性疼痛和重性抑郁障碍之间存在着很大的共病和相似性。我们最近发现,10 天的社交挫败应激(SDS)会导致小鼠产生痛觉过敏,而不会出现类似抑郁的行为。在这里,我们旨在研究社交应激是否会导致慢性疼痛,以及相反,慢性疼痛是否会导致应激引起的抑郁。
首先,我们在小鼠中使用 10 天 SDS 范式,然后使用轻度重复炎症刺激方案来评估 SDS 是否会导致持续的痛觉过敏发展。其次,我们使用强烈的重复炎症刺激方案,然后使用亚阈 SDS 来评估持续的痛觉过敏是否会导致社交回避的类似抑郁行为。
我们的结果表明,SDS 会导致慢性疼痛,因为接受 PGE2 注射 7 天的应激小鼠(轻度方案),通常不会引起慢性疼痛的刺激,表现出持续的痛觉过敏。此外,我们还表明,由重复炎症刺激引起的持续痛觉过敏会导致由亚阈 SDS 引起的持久的社交回避类似抑郁行为。
我们没有分析与 SDS 引起的慢性疼痛和类似抑郁行为相关的分子机制。然而,我们假设 SDS 和 14 天的 PGE2 会在慢性疼痛和抑郁共有的大脑区域产生神经可塑性,分别导致疼痛的慢性化和类似抑郁的行为。
我们可以得出结论,社交应激是慢性疼痛和抑郁的一个关键和共同因素。我们还可以得出结论,SDS 会导致慢性疼痛,而相反,慢性疼痛会导致类似抑郁的行为。