La Porta C, Lara-Mayorga I M, Negrete R, Maldonado R
Laboratory of Neuropharmacology, Department of Experimental and Health Science, Pompeu Fabra University (CEXS-UPF), Barcelona, Spain.
Eur J Pain. 2016 Oct;20(9):1454-66. doi: 10.1002/ejp.868. Epub 2016 Mar 31.
Preclinical drug discovery for the treatment of chronic pain is at present challenged by the difficulty to study behaviours comparable to the complex human pain experience in animals. Several reports have demonstrated a frequent association of chronic pain in humans with affective disorders, such as anxiety and depression, and impaired cognitive functions, including memory and decision making, and motivation for goal-directed behaviours. In this study, we validated different behavioural outcomes to measure the emotional and cognitive manifestations of neuropathic pain induced in mice by partial sciatic nerve ligation.
In these mice, we evaluated at different time points the nociceptive responses, the anxiety- and depressive-like behaviours, the anhedonic state, object recognition memory and the operant responding maintained by food and the effects of the repeated administration of pregabalin on these manifestations.
Our results demonstrated that the presence of allodynia and hyperalgesia in neuropathic pain mice was associated with increased anxiety- and depressive-like behaviours, reduced memory functions, development of an anhedonic state and impaired motivation to obtain food in the operant task. Chronic pregabalin treatment improved the nociceptive, anxiety-like and anhedonic responses, as well as the memory deficit, but did not modify the depressive-like alterations and the decreased motivation in these mice.
These results indicate that some emotional manifestations of chronic pain do not necessarily resolve when pain is relieved and underline the relevance to evaluate multiple behavioural responses associated with chronic pain, including the affective-motivational and cognitive behaviours, to increase the predictive value of preclinical drug discovery. WHAT DOES THIS STUDY ADD?: In this study, we have validated different behavioural outcomes allowing a reliable measurement of the emotional and cognitive manifestations of neuropathic pain induced in mice by partial sciatic nerve ligation. These results underline the relevance to evaluate these multiple pain-related alterations to improve the predictive value of preclinical drug discovery.
目前,用于治疗慢性疼痛的临床前药物研发面临挑战,因为在动物身上难以研究与复杂的人类疼痛体验相似的行为。多项报告表明,人类慢性疼痛常与情感障碍(如焦虑和抑郁)以及认知功能受损(包括记忆、决策和目标导向行为的动机)相关联。在本研究中,我们验证了不同的行为结果,以测量部分坐骨神经结扎诱导的小鼠神经性疼痛的情绪和认知表现。
在这些小鼠中,我们在不同时间点评估了伤害性反应、焦虑样和抑郁样行为、快感缺失状态、物体识别记忆以及由食物维持的操作性反应,以及普瑞巴林重复给药对这些表现的影响。
我们的结果表明,神经性疼痛小鼠中的痛觉过敏和异常性疼痛与焦虑样和抑郁样行为增加、记忆功能降低、快感缺失状态的发展以及操作性任务中获取食物的动机受损有关。慢性普瑞巴林治疗改善了伤害性、焦虑样和快感缺失反应以及记忆缺陷,但并未改变这些小鼠的抑郁样改变和动机降低。
这些结果表明,慢性疼痛的一些情绪表现不一定在疼痛缓解时得到解决,并强调评估与慢性疼痛相关的多种行为反应(包括情感动机和认知行为)的相关性,以提高临床前药物研发的预测价值。本研究补充了什么?:在本研究中,我们验证了不同的行为结果,能够可靠地测量部分坐骨神经结扎诱导的小鼠神经性疼痛的情绪和认知表现。这些结果强调了评估这些与疼痛相关的多种改变以提高临床前药物研发预测价值的相关性。