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Effects of Acute and Sustained Pain Manipulations on Performance in a Visual‐Signal Detection Task of Attention in Rats

机译:急性和持续性疼痛操作对大鼠注意力视觉信号检测任务的影响

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摘要

Preclinical ResearchPatients with pain often display cognitive impairment including deficits in attention. The visual‐signal detection task (VSDT) is a behavioral procedure for assessment of attention in rodents. Male Sprague Dawley rats were trained in a VSDT and tested with three different noxious stimuli: (i) intraperitoneal injection of lactic acid; (ii) intraplantar injection of formalin; and (iii) intraplantar injection of complete Freund's adjuvant (CFA). The muscarinic acetylcholine receptor antagonist, scopolamine was also tested as a positive control. Scopolamine (0.01–1.0 mg/kg) dose dependently reduced accuracy and increased response latencies during completed trials with higher scopolamine doses increasing omissions. Lactic acid (0.56–5.6% ip) also increased response latencies and omissions, although it failed to alter measures of response accuracy. Formalin produced a transient decrease in accuracy while also increasing both response latency and omissions. CFA failed to alter VSDT performance. Although VSDT effects were transient for formalin and absent for CFA, both treatments produced mechanical allodynia and paw edema for up to 7 days. These results support the potential for noxious stimuli to produce a pain‐related disruption of attention in rats. However, relatively strong noxious stimulation appears necessary to disrupt performance in this version of the VSDT. Drug Dev Res 76 : 194–203, 2015. © 2015 Wiley Periodicals, Inc.
机译:临床前研究患有疼痛的患者经常表现出认知障碍,包括注意力不足。视觉信号检测任务(VSDT)是一种用于评估啮齿动物注意力的行为程序。在VSDT中对雄性Sprague Dawley大鼠进行训练,并用三种不同的有害刺激进行测试:(i)腹膜内注射乳酸; (ii)足底注射福尔马林; (iii)足底注射完全弗氏佐剂(CFA)。还测试了毒蕈碱型乙酰胆碱受体拮抗剂东pol碱作为阳性对照。在完成的试验中,东co碱(0.01–1.0 mg / kg)剂量会相应降低准确性,并增加响应潜伏期,而东pol碱剂量较高则会增加遗漏。乳酸(0.56-5.6%ip)也增加了响应潜伏期和遗漏,尽管它不能改变响应准确度的指标。福尔马林造成准确性的暂时下降,同时也增加了响应潜伏期和遗漏率。 CFA无法更改VSDT性能。尽管福尔马林的VSDT效果是短暂的,而CFA则不存在,但两种治疗均产生机械性异常性疼痛和爪水肿长达7天。这些结果支持了有害刺激在大鼠中引起疼痛相关的注意力破坏的潜力。但是,在此版本的VSDT中,似乎需要相对较强的有害刺激来破坏性能。 Drug Dev Res 76:194–203,2015。©2015 Wiley Periodicals,Inc.

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