Tuboly Gabor, Benedek György, Horvath Gyöngyi
Department of Physiology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Physiol Behav. 2009 Jan 8;96(1):18-22. doi: 10.1016/j.physbeh.2008.07.030. Epub 2008 Aug 15.
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.
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。