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Effects of mu- and kappa-2 opioid receptor agonists on pain and rearing behaviors

机译:mu-和kappa-2阿片受体激动剂对疼痛和抚养行为的影响

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Background Management of pain involves a balance between inhibition of pain and minimization of side effects; therefore, in developing new analgesic compounds, one must consider the effects of treatment on both pain processing and behavior. The purpose of this study was to evaluate the effects of the mu and kappa-2 opioid receptor agonists on general and pain behavioral outcomes. Methods As a general behavioral assessment, we modified the cylinder rearing assay and recorded the number and duration of rearing events. Thermal sensitivity was evaluated using either a reflexive measure of hindpaw withdrawal latency to a radiant heat source or using an orofacial operant thermal assay. Acetic acid-induced visceral pain and capsaicin-induced neurogenic inflammatory pain were used as painful stimuli. The mu-opioid receptor agonist, morphine or the kappa-2 receptor agonist GR89696 was administered 30 min prior to testing. A general linear model repeated measures analysis was completed for baseline session comparisons and an analysis of variance was used to evaluate the effects of treatment on each outcome measure (SPSS Inc). When significant differences were found, post-hoc comparisons were made using the Tukey honestly significant difference test. *P Results We found that morphine and GR89,696 dose-dependently decreased the number of reaching events and rearing duration. Rearing behavior was not affected at 0.5 mg/kg for morphine, 1.25 × 10-4 mg/kg for GR89,696. Hindpaw thermal sensitivity was significantly increased only at the highest doses for each drug. At the highest dose that did not significantly influence rearing behavior, we found that visceral and neurogenic inflammatory pain was not affected following GR89,696 administration and morphine was only partially effective for blocking visceral pain. Conclusion This study demonstrated that high levels of the opioids produced significant untoward effects and made distinguishing an analgesic versus a more general effect more difficult. Quantification of rearing behavior in conjunction with standard analgesic assays can help in gaining a better appreciation of true analgesic efficacy of experimental drugs.
机译:背景技术疼痛的治疗涉及疼痛抑制和副作用最小化之间的平衡。因此,在开发新的止痛药时,必须考虑治疗对疼痛处理和行为的影响。这项研究的目的是评估mu和kappa-2阿片受体激动剂对一般和疼痛行为结局的影响。方法作为一般的行为评估,我们修改了气瓶饲养试验并记录了饲养事件的数量和持续时间。使用反射性测量后脚退缩到辐射热源的潜伏期或使用口面操作热测定法评估热敏感性。乙酸引起的内脏疼痛和辣椒素引起的神经源性炎性疼痛被用作疼痛刺激。在测试前30分钟施用mu阿片类受体激动剂,吗啡或kappa-2受体激动剂GR89696。完成了用于基线会话比较的常规线性模型重复测量分析,并使用方差分析评估了治疗对每种结局测量的影响(SPSS Inc)。当发现显着差异时,使用Tukey诚实的显着差异测试进行事后比较。 * P结果我们发现吗啡和GR89,696剂量依赖性地减少了到达事件的次数和饲养时间。吗啡为0.5 mg / kg,GR89,696为1.25×10 -4 mg / kg时,饲养行为不受影响。仅在每种药物的最高剂量下,后爪的热敏感性才显着增加。在不显着影响饲养行为的最高剂量下,我们发现GR89696给药后内脏和神经源性炎性疼痛不受影响,吗啡仅部分有效地阻断了内脏疼痛。结论这项研究表明,高剂量的阿片类药物产生明显的不良作用,使镇痛药与更一般的镇痛作用区分开来更加困难。结合标准的镇痛方法对饲养行为进行量化可以帮助更好地了解实验药物的真正镇痛效果。

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