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社交隔离后疼痛敏感性的选择性干扰。

Selective disturbance of pain sensitivity after social isolation.

作者信息

Tuboly Gabor, Benedek György, Horvath Gyöngyi

机构信息

Department of Physiology, Faculty of Medicine, University of Szeged, Szeged, Hungary.

出版信息

Physiol Behav. 2009 Jan 8;96(1):18-22. doi: 10.1016/j.physbeh.2008.07.030. Epub 2008 Aug 15.

Abstract

The effects of social isolation or NMDA-receptor antagonists on pain sensitivity have repeatedly been described. However, the mechanisms underlying the alterations of pain perception in these models still remain a matter of debate. Thus, we aimed to determine the long-lasting effects of subchronic ketamine treatment and social isolation on the C- and Adelta-fiber-mediated nociception. Wistar rats after weaning (21-23 days old) were either housed individually or grouped for 21 days. The animals were treated daily for 14 days with either ketamine (30 mg/kg) or saline. On the 21st day, tail-flick latency was determined at 48 degrees C (C-fiber activation) and 52 degrees C (affects mainly Adelta-fibers), and rats were rehoused. Tail-flick test was repeated 2 and 4 weeks later. On the 5th week, carrageenan-induced heat hyperalgesia was determined on paw-withdrawal test before and after morphine treatment (1, 2 or 3 mg/kg). Regarding tail-flick latencies at 48 degrees C, juvenile isolation, but not ketamine resulted in a significantly enhanced pain threshold (p<0.001) throughout the investigation period, while the changes at 52 degrees C were not significant. In addition, both isolation and ketamine treatments enhanced the antihyperalgesic effect of 2 mg/kg morphine. In summary, juvenile isolation exerts a long-lasting effect on acute heat pain sensitivity, disturbing primarily the C-fiber-linked pain pathways, suggesting a selective disruption in the parallel sensory pathways. Since both social isolation and NMDA treatment are well-known animal models of schizophrenia, our results showed that juvenile isolation but not ketamine administration can simulate hypoalgesia associated with this disease.

摘要

社会隔离或NMDA受体拮抗剂对疼痛敏感性的影响已被多次描述。然而,在这些模型中疼痛感知改变的潜在机制仍然存在争议。因此,我们旨在确定亚慢性氯胺酮治疗和社会隔离对C纤维和Aδ纤维介导的伤害感受的长期影响。断奶后(21 - 23日龄)的Wistar大鼠要么单独饲养,要么分组饲养21天。动物每天接受14天的氯胺酮(30mg/kg)或生理盐水治疗。在第21天,测定48℃(C纤维激活)和52℃(主要影响Aδ纤维)时的甩尾潜伏期,然后将大鼠重新安置。在2周和4周后重复甩尾试验。在第5周,在吗啡治疗(1、2或3mg/kg)前后的爪部退缩试验中测定角叉菜胶诱导的热痛觉过敏。关于48℃时的甩尾潜伏期,在整个研究期间,幼年隔离而非氯胺酮导致疼痛阈值显著提高(p<0.001),而52℃时的变化不显著。此外,隔离和氯胺酮治疗均增强了2mg/kg吗啡的抗痛觉过敏作用。总之,幼年隔离对急性热痛敏感性有长期影响,主要干扰与C纤维相关的疼痛通路,提示在平行感觉通路中有选择性破坏。由于社会隔离和NMDA治疗都是众所周知的精神分裂症动物模型,我们的结果表明,幼年隔离而非氯胺酮给药可以模拟与该疾病相关的痛觉减退。

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