Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Department of Biochemistry, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Burns. 2021 Dec;47(8):1896-1907. doi: 10.1016/j.burns.2021.04.010. Epub 2021 Apr 20.
Acute pain is prevalent following burn injury and can often transition to chronic pain. Prolonged acute pain is an important risk factor for chronic pain and there is little preclinical research to address this problem. Using a mouse model of second-degree burn, we investigated whether pre-existing stress influences pain(sensitivity) after a burn injury. We introduced a contribution of stress in two different ways: (1) the use of foot-shock as a pre-injury stressor or (2) the use of A/J mice to represent higher pre-existing stress compared to C57Bl/6 mice. C57Bl/6 and A/J mice were exposed to repeated mild foot shock to induce stress for 10 continuous days and mice underwent either burn injury or sham burn injury of the plantar surface of the right hind paw. Assessments of mechanical and thermal sensitivities of the injured and uninjured paw were conducted during the shock protocol and at intervals up to 82-day post-burn injury. In both strains of mice that underwent burn injury, thermal hypersensitivity and mechanical allodynia appeared rapidly in the ipsilateral paw. Mice that were stressed took much longer to recover their hind paw mechanical thresholds to baseline compared to non-stressed mice in both burn and non-burn groups. Analysis of the two mouse strains revealed that the recovery of mechanical thresholds in A/J mice which display higher levels of baseline anxiety was shorter than C57Bl/6 mice. No differences were observed regarding thermal sensitivities between strains. Our results support the view that stress exposure prior to burn injury affects mechanical and thermal thresholds and may be relevant to as a risk factor for the transition from acute to chronic pain. Finally, genetic differences may play a key role in modality-specific recovery following burn injury.
急性疼痛在烧伤后很常见,并且常常会转变为慢性疼痛。长期的急性疼痛是慢性疼痛的一个重要危险因素,而目前针对这个问题的临床前研究还很少。本研究使用二度烧伤小鼠模型,研究了烧伤前的应激是否会影响烧伤后的疼痛敏感性。我们通过两种方式引入了应激的作用:(1)使用足底电击作为损伤前的应激源;或(2)使用 A/J 小鼠来代表比 C57Bl/6 小鼠更高的预先存在的应激。C57Bl/6 和 A/J 小鼠接受重复的轻度足底电击,以连续 10 天诱导应激,然后对右后爪的足底表面进行烧伤或假烧伤。在电击方案期间以及烧伤后 82 天内的不同时间点,评估损伤和未损伤爪子的机械和热敏感性。在接受烧伤的两种小鼠品系中,热超敏反应和机械性痛觉过敏在同侧爪子中迅速出现。与非应激小鼠相比,应激小鼠在烧伤和非烧伤组中都需要更长的时间才能使后爪的机械阈值恢复到基线。对两种小鼠品系的分析表明,在基线焦虑水平较高的 A/J 小鼠中,机械阈值的恢复速度快于 C57Bl/6 小鼠。在两种品系之间,热敏感性没有差异。我们的研究结果支持了这样一种观点,即烧伤前的应激暴露会影响机械和热阈值,并可能与从急性疼痛向慢性疼痛的转变有关。最后,遗传差异可能在烧伤后的特定模式恢复中起关键作用。