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Increased anxiety-like behaviors in rats experiencing chronic inflammatory pain

机译:患有慢性发炎性疼痛的大鼠的焦虑样行为增加

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For many patients, chronic pain is often accompanied, and sometimes amplified, by co-morbidities such as anxiety and depression. Although it represents important challenges, the establishment of appropriate preclinical behavioral models contributes to drug development for treating chronic inflammatory pain and associated psychopathologies. In this study, we investigated whether rats experiencing persistent inflammatory pain induced by intraplantar injection of complete Freund's adjuvant (CFA) developed anxiety-like behaviors, and whether clinically used analgesic and anxiolytic drugs were able to reverse CFA-induced anxiety-related phenotypes. These behaviors were evaluated over 28 days in both CFA- and saline-treated groups with a variety of behavioral tests. CFA-induced mechanical allodynia resulted in increased anxiety-like behaviors as evidenced by: (1) a significant decrease in percentage of time spent and number of entries in open arms of the elevated-plus maze (EPM), (2) a decrease in number of central squares visited in the open field (OF), and (3) a reduction in active social interactions in the social interaction test (SI). The number of entries in closed arms in the EPM and the distance traveled in the OF used as indicators of locomotor performance did not differ between treatments. Our results also reveal that in CFA-treated rats, acute administration of morphine (3. mg/kg, s.c.) abolished tactile allodynia and anxiety-like behaviors, whereas acute administration of diazepam (1. mg/kg, s.c) solely reversed anxiety-like behaviors. Therefore, pharmacological treatment of anxiety-like behaviors induced by chronic inflammatory pain can be objectively evaluated using multiple behavioral tests. Such a model could help identify/validate alternative potential targets that influence pain and cognitive dimensions of anxiety.
机译:对于许多患者来说,慢性疼痛通常伴随着焦虑症和抑郁症,有时甚至并发。尽管这代表着重要的挑战,但建立适当的临床前行为模型有助于治疗慢性炎症性疼痛和相关精神病学的药物开发。在这项研究中,我们调查了通过足底弗氏完全佐剂(CFA)足底注射引起的持续性炎性疼痛的大鼠是否表现出焦虑样行为,以及临床使用的镇痛药和抗焦虑药是否能够逆转CFA诱导的焦虑症相关表型。这些行为在28天的CFA和盐水治疗组中通过各种行为测试进行了评估。 CFA引起的机械性异常性疼痛导致焦虑样行为增加,其表现为:(1)花费的时间百分比和高架迷宫(EPM)的张开双臂进入次数显着减少,(2)开放领域(OF)中访问的中心广场的数量,以及(3)社交互动测试(SI)中主动社交互动的减少。 EPM中闭合臂的进入数量和OF中作为运动性能指标的行进距离在不同处理之间没有差异。我们的研究结果还表明,在接受CFA治疗的大鼠中,吗啡的急性给药(3. mg / kg,sc)消除了触觉异常性疼痛和类似焦虑的行为,而地西epa的急性给药(1. mg / kg,sc)却完全消除了焦虑。行为。因此,可以使用多种行为测试客观地评估由慢性炎症性疼痛引起的焦虑样行为的药物治疗。这种模型可以帮助识别/验证影响疼痛和焦虑认知范围的替代性潜在目标。

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