Roeska Kerstin, Doods Henri, Arndt Kirsten, Treede Rolf-Detlef, Ceci Angelo
Department of CNS Research, Boehringer Ingelheim Pharma GmbH & Co. KG, Birkendorfer Straße 65, 88397 Biberach an der Riss, Germany Center for Biomedicine and Medical Technology Mannheim (CBTM), Ruprecht-Karls-University Heidelberg, Ludolf-Krehl-Straße 13-17, 68167 Mannheim, Germany.
Pain. 2008 Oct 15;139(2):349-357. doi: 10.1016/j.pain.2008.05.003. Epub 2008 Jun 18.
Anxiety has been described as an important comorbidity in patients suffering from chronic pain. However, in animals the connection between persistent pain and anxiety has hardly been investigated. Therefore, in the current study it was assessed whether chronic pain also causes anxiety-like behaviour in animals and if it can be reversed by analgesic or anxiolytic drugs. Neuropathic pain was induced in rats by partial sciatic nerve ligation (PNL) and chronic constriction injury (CCI). Mechanical hypersensitivity was assessed by the "electronic algometer", while anxiety-like behaviour was measured by using the elevated plus maze. In both neuropathic pain models, rats exhibited mechanical hypersensitivity, whereas a significant increase in anxiety-like behaviour was observed only in CCI rats (time spent in open arms decreased significantly from 99+/-15.8s in sham animals to 33.4+/-7.5s in CCI animals). Furthermore, midazolam (0.5mg/kg; i.p.) significantly reduced anxiety-like behaviour in both sham- and CCI-operated animals without influencing mechanical hypersensitivity. Morphine (3mg/kg; i.p.) and gabapentin (30 mg/kg; i.p.) significantly attenuated anxiety-like behaviour in the CCI lesioned rats: morphine increased entries into open arms from 3.0+/-0.4 to 7.7+/-1.4 (P=0.01), gabapentin elevated this value from 4.7+/-1 to 7.5+/-0.9 (P=0.02). These data suggest that rats subjected to neuropathic pain models develop anxiety-like behaviour which can be reversed by appropriate analgesic treatment. Morphine and gabapentin had no anxiolytic-like effect in sham treated animals, thus their effect on anxiety-like behaviour in the neuropathic pain model is likely indirect via their anti-nociceptive properties.
焦虑被认为是慢性疼痛患者的一种重要共病。然而,在动物中,持续性疼痛与焦虑之间的联系几乎未被研究过。因此,在本研究中,评估了慢性疼痛是否也会导致动物出现焦虑样行为,以及这种行为是否能被镇痛或抗焦虑药物逆转。通过部分坐骨神经结扎(PNL)和慢性压迫损伤(CCI)在大鼠中诱导神经性疼痛。使用“电子痛觉计”评估机械性超敏反应,同时使用高架十字迷宫测量焦虑样行为。在两种神经性疼痛模型中,大鼠均表现出机械性超敏反应,而仅在CCI大鼠中观察到焦虑样行为显著增加(在开放臂停留的时间从假手术动物的99±15.8秒显著减少至CCI动物的33.4±7.5秒)。此外,咪达唑仑(0.5mg/kg;腹腔注射)显著降低了假手术和CCI手术动物的焦虑样行为,而不影响机械性超敏反应。吗啡(3mg/kg;腹腔注射)和加巴喷丁(30mg/kg;腹腔注射)显著减轻了CCI损伤大鼠的焦虑样行为:吗啡使进入开放臂的次数从3.0±0.4增加至7.7±1.4(P = 0.01),加巴喷丁将该值从4.7±1提高至7.5±0.9(P = 0.02)。这些数据表明,经历神经性疼痛模型的大鼠会出现焦虑样行为,这种行为可通过适当的镇痛治疗逆转。吗啡和加巴喷丁在假手术动物中没有抗焦虑样作用,因此它们在神经性疼痛模型中对焦虑样行为的作用可能是通过其抗伤害感受特性间接产生的。