Department of Pharmacology and Toxicology and Translational Research Initiative for Pain and Neuropathy, Virginia Commonwealth University, Virginia Commonwealth University, Richmond, VA 23298-0613, USA.
Department of Pharmacology and Toxicology and Translational Research Initiative for Pain and Neuropathy, Virginia Commonwealth University, Virginia Commonwealth University, Richmond, VA 23298-0613, USA.
Behav Brain Res. 2020 Jul 15;390:112698. doi: 10.1016/j.bbr.2020.112698. Epub 2020 May 16.
Substantial evidence from preclinical models of pain suggests that basal and noxious nociceptive sensitivity, as well as antinociceptive responses to drugs, show significant heritability. Individual differences to these responses have been observed across species from rodents to humans. The use of closely related C57BL/6 inbred mouse substrains can facilitate gene mapping of acute nociceptive behaviors in preclinical pain models. In this study, we investigated behavioral differences between C57BL/6 J (B6 J) and C57BL/6 N (B6 N) substrains in the formalin test, a widely used tonic inflammatory pain model, using a battery of pain-related phenotypes, including reflexive tests, nesting, voluntary wheel running, sucrose preference and anxiety-like behavior in the light/dark test at two different time points (1-h and 24-h). Our results show that these substrains did not differ in reflexive thermal and mechanical responses at the 1-h time point. However, B6 N substrain mice showed increased sensitivity to spontaneous pain-like behaviors. In addition, B6 N substrain continued to show higher levels of mechanical hypersensitivity compared to controls at 24-h. indicating that mechanical hypersensitivity is a more persistent pain-related phenotype induced by formalin. Finally, no sex differences were observed in our outcome measures. Our results provide a comprehensive behavioral testing paradigm in response to an inflammatory agent for future mouse genetic studies in pain.
大量的临床前疼痛模型证据表明,基础和伤害性疼痛敏感性以及药物的抗伤害性反应具有显著的遗传性。从啮齿动物到人类等不同物种都观察到了这些反应的个体差异。使用近交系 C57BL/6 亚系可以促进临床前疼痛模型中急性疼痛行为的基因图谱绘制。在这项研究中,我们使用一系列与疼痛相关的表型,包括反射测试、筑巢、自愿轮跑、蔗糖偏好和在光/暗测试中的焦虑样行为,在福马林测试中研究了 C57BL/6 J(B6 J)和 C57BL/6 N(B6 N)亚系之间的行为差异,福马林测试是一种广泛使用的强直性炎症性疼痛模型。我们的结果表明,这两个亚系在 1 小时时间点的反射性热和机械反应没有差异。然而,B6 N 亚系小鼠对自发性疼痛样行为的敏感性增加。此外,与对照组相比,B6 N 亚系在 24 小时时仍表现出更高水平的机械性超敏反应,表明机械性超敏反应是福马林引起的更持久的与疼痛相关的表型。最后,我们的研究结果没有观察到性别差异。我们的结果为未来的疼痛小鼠遗传研究提供了一种对炎症剂的全面行为测试范式。