Heterogeneity in patterns of pain development after nerve injury in rats and the influence of sex

Q2 Medicine Neurobiology of Pain Pub Date : 2021-08-01 DOI:10.1016/j.ynpai.2021.100069
Katherine Sherman , Victoria Woyach , James C. Eisenach , Francis A. Hopp , Freddy Cao , Quinn H. Hogan , Caron Dean
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引用次数: 3

Abstract

The genesis of neuropathic pain is complex, as sensory abnormalities may differ between patients with different or similar etiologies, suggesting mechanistic heterogeneity, a concept that is largely unexplored. Yet, data are usually grouped for analysis based on the assumption that they share the same underlying pathogenesis. Sex is a factor that may contribute to differences in pain responses. Neuropathic pain is more prevalent in female patients, but pre-clinical studies that can examine pain development in a controlled environment have typically failed to include female subjects. This study explored patterns of development of hyperalgesia-like behavior (HLB) induced by noxious mechanical stimulation in a neuropathic pain model (spared nerve injury, SNI) in both male and female rats, and autonomic dysfunction that is associated with chronic pain. HLB was analyzed across time, using both discrete mixture modeling and rules-based longitudinal clustering. Both methods identified similar groupings of hyperalgesia trajectories after SNI that were not evident when data were combined into groups by sex only. Within the same hyperalgesia development group, mixed models showed that development of HLB in females was delayed relative to males and reached a magnitude similar to or higher than males. The data also indicate that sympathetic tone (as indicated by heart rate variability) drops below pre-SNI level before or at the onset of development of HLB. This study classifies heterogeneity in individual development of HLB and identifies sexual dimorphism in the time course of development of neuropathic pain after nerve injury. Future studies addressing mechanisms underlying these differences could facilitate appropriate pain treatments.

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大鼠神经损伤后疼痛发展模式的异质性及性别的影响
神经性疼痛的发生是复杂的,因为不同或相似病因的患者的感觉异常可能不同,这表明机制异质性,这是一个很大程度上未被探索的概念。然而,数据通常是基于它们具有相同的潜在发病机制的假设进行分组分析的。性别可能是导致疼痛反应差异的一个因素。神经性疼痛在女性患者中更为普遍,但可以在受控环境中检查疼痛发展的临床前研究通常未能包括女性受试者。本研究探讨了雄性和雌性大鼠神经性疼痛模型(SNI)中有害机械刺激诱导的痛觉过敏样行为(HLB)的发展模式,以及与慢性疼痛相关的自主神经功能障碍。利用离散混合建模和基于规则的纵向聚类对HLB进行了跨时间分析。两种方法都确定了SNI后痛觉过敏轨迹的相似分组,当数据仅按性别分组时,这种分组并不明显。在同一个痛觉过敏发展组中,混合模型显示,女性HLB的发展相对于男性延迟,并且达到与男性相似或更高的程度。数据还表明,交感神经张力(如心率变异性所示)在HLB发生之前或开始时降至sni前水平以下。本研究对HLB个体发展的异质性进行了分类,并在神经损伤后神经性疼痛的发展过程中确定了性别二态性。未来的研究解决这些差异背后的机制可以促进适当的疼痛治疗。
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来源期刊
Neurobiology of Pain
Neurobiology of Pain Medicine-Anesthesiology and Pain Medicine
CiteScore
4.40
自引率
0.00%
发文量
29
审稿时长
54 days
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