Liu Yan, Yang Liu, Yu Jin, Zhang Yu-Qiu
Institute of Neurobiology, Institutes of Brain Science and State Key Laboratory of Medical Neurobiology, Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China.
Institute of Neurobiology, Institutes of Brain Science and State Key Laboratory of Medical Neurobiology, Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China; Department of Integrative Medicine and Neurobiology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Physiol Behav. 2015 Nov 1;151:55-63. doi: 10.1016/j.physbeh.2015.07.004. Epub 2015 Jul 10.
Clinically, pain and anxiety frequently coexist; however, these two conditions' interaction is limited and contradictory in animal studies. In this study, we combined social defeat (SD) stress with Freund's adjuvant (CFA)-induced persistent inflammatory pain to investigate the reciprocal relationship between anxiety-like and nociceptive behaviors in two mouse strains. C57BL/6J mice subjected to the 10-day period of SD stress by repeated CD-1 mice aggression exhibited significant social interaction avoidance behaviors in the social interaction (SI) test, which is believed to represent the symptoms of anxiety. These mice also displayed anxiety-like behaviors in elevated plus maze (EPM) and open field (OF) tests. Compared to C57BL/6J mice, FVB/NJNju mice showed less basal social contact, but their behavioral responses to 10-day SD stress were more resilient. CFA-inflammatory mice showed robust mechanical allodynia and thermal hyperalgesia in both strains, but did not develop obvious social avoidance and anxiety-like behaviors 10 days after CFA-inflammation. Interestingly, CFA-inflammatory mice exposed to SD stress were not accompanied by a worsening of pain and anxiety-like behaviors in most tests. In contrast, the SD stress-induced social avoidance was significantly antagonized by combining with CFA-inflammatory pain. These findings suggest that persistent inflammatory pain and SD stress-induced anxiety may not necessarily exacerbate one another in animal models of comorbidity.
临床上,疼痛和焦虑常常同时存在;然而,在动物研究中,这两种情况的相互作用有限且相互矛盾。在本研究中,我们将社会挫败(SD)应激与弗氏完全佐剂(CFA)诱导的持续性炎性疼痛相结合,以研究两种小鼠品系中焦虑样行为与伤害感受行为之间的相互关系。通过反复遭受CD-1小鼠攻击而经历10天SD应激的C57BL/6J小鼠在社会互动(SI)测试中表现出显著的社会互动回避行为,这被认为代表焦虑症状。这些小鼠在高架十字迷宫(EPM)和旷场(OF)测试中也表现出焦虑样行为。与C57BL/6J小鼠相比,FVB/NJNju小鼠的基础社会接触较少,但它们对10天SD应激的行为反应更具恢复力。CFA炎性小鼠在两种品系中均表现出强烈的机械性痛觉过敏和热痛觉过敏,但在CFA炎症后10天未出现明显的社会回避和焦虑样行为。有趣的是,在大多数测试中,暴露于SD应激的CFA炎性小鼠并未伴随疼痛和焦虑样行为的恶化。相反,与CFA炎性疼痛相结合可显著拮抗SD应激诱导的社会回避。这些发现表明,在共病动物模型中,持续性炎性疼痛和SD应激诱导的焦虑不一定会相互加剧。