首页> 外文期刊>European journal of pain : >Scopolamine into the anterior cingulate cortex diminishes nociception in a neuropathic pain model in the rat: an interruption of 'nociception-related memory acquisition'?
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Scopolamine into the anterior cingulate cortex diminishes nociception in a neuropathic pain model in the rat: an interruption of 'nociception-related memory acquisition'?

机译:东co碱进入前扣带回皮质会减少大鼠神经性疼痛模型中的伤害感受:“伤害感受相关的记忆获取”的中断吗?

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The cingulate cortex plays a key role in the affective component related to pain perception. This structure receives cholinergic projections and also plays a role in memory processing. Therefore, we propose that the cholinergic system in the anterior cingulate cortex is involved in the nociceptive memory process. We used scopolamine (10 microg in 0.25 mircrol/saline) microinjected into the anterior cingulate cortex, either before thermonociception followed by a sciatic denervation, between thermonociception and denervation or after both procedures (n=10 each). The vehicle group (saline solution 0.9%, n=14) was microinjected before thermonociception. Chronic nociception was measured by the autotomy score, which onset and incidence were also determined. Group scopolamine-thermonociception-denervation (STD) presented the lowest autotomy score as compared to vehicle and group thermonociception-denervation-scopolamine (TDS) (vehicle vs. STD, p=0.002, STD vs. TDS, p=0.001). Group thermonociception-scopolamine-denervation (TSD) showed a diminished autotomy score when compared to TDS (p=0.053). STD group showed a delay in the onset of AB as compared to the rest of the groups. Group TSD presented a significative delay (p=0.048) in AB onset when compared to group TDS. There were no differences in the incidence between groups. The results show that nociception-related memory processed in the anterior cingulate cortex is susceptible of being modified by the cholinergic transmission blockade. When scopolamine is microinjected prior to the nociceptive stimuli, nociception-related memory acquisition is prevented. The evidence obtained in this study shows the role of the anterior cingulate cortex in the acquisition of nociception-related memory.
机译:扣带回皮层在与疼痛感相关的情感成分中起关键作用。该结构接受胆碱能投射,并且在记忆处理中也起作用。因此,我们建议前扣带回皮层中的胆碱能系统参与伤害性记忆过程。我们在热伤害感受后再进行坐骨神经去神经支配,热伤害感受和去神经支配之间或两种方法之后(每组n = 10),将东pol碱(0.25微克尔/盐水中的10微克)微注射入前扣带回皮层。在热伤害感受之前,微注射媒介物组(盐溶液0.9%,n = 14)。慢性疼痛通过自动切开评分来衡量,并确定发作和发病率。与媒介物和组热伤害感受-去神经-东pol碱(TDS)相比,东pol碱-热感受器-神经变性(STD)组的自体解剖评分最低(车辆与STD,p = 0.002,STD与TDS,p = 0.001)。与TDS相比,组热伤害感受-东pol碱-去神经支配(TSD)的自动切开术评分降低(p = 0.053)。与其他组相比,STD组的AB发作有所延迟。与TDS组相比,TSD组在AB发作方面表现出显着的延迟(p = 0.048)。两组之间的发生率没有差异。结果表明,在前扣带回皮层中处理的伤害感受相关记忆易受胆碱能传递阻滞的影响。当在伤害性刺激之前显微注射东pol碱时,可以防止伤害性记忆相关的记忆获得。在这项研究中获得的证据表明前扣带回皮层在伤害感受相关记忆的获得中的作用。

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