...
首页> 外文期刊>Neuropeptides: An International Journal >Differential effects of acute morphine, and chronic morphine-withdrawal on obsessive-compulsive behavior: Inhibitory influence of CRF receptor antagonists on chronic morphine-withdrawal
【24h】

Differential effects of acute morphine, and chronic morphine-withdrawal on obsessive-compulsive behavior: Inhibitory influence of CRF receptor antagonists on chronic morphine-withdrawal

机译:急性吗啡和慢性吗啡戒断对强迫症行为的差异作用:CRF受体拮抗剂对慢性吗啡戒断的抑制作用

获取原文
获取原文并翻译 | 示例
           

摘要

Recent studies have provided convincing evidences for co-morbidity between opioid addiction and obsessive-compulsive disorder (OCD), and the involvement of the corticotrophin-releasing factor (CRF) in the effects of morphine-withdrawal. Some scanty evidences also point towards the role of CRF in OCD and related disorders. But, no evidence indicated the role of CRF in morphine withdrawal associated obsessive-compulsive behavior (OCB). Therefore, the present study investigated the role of CRF in morphine-withdrawal induced OCB in mice. Marble-burying behavior in mice was used to assess OCB as this model has good predictive and face validity. The results revealed that acute morphine dose dependently attenuated the marble burying behavior, whereas withdrawal of chronic morphine was associated with significant rise in marble burying behavior. This indicates the differential effect of acute morphine and chronic morphine-withdrawal on OCB. Further, acute treatment with CRF receptor antagonists like antalarmin (2 and 4. μg/mouse, i.c.v.) or astressin-2B (3 and 10. nmol/mouse, i.c.v.) dose dependently attenuated the peak morphine-withdrawal induced increase in marble burying behavior. Moreover, concomitant treatment with antalarmin (4. μg/mouse, i.c.v.) or astressin-2B (10. nmol/mouse, i.c.v.) along with morphine blocked the morphine-withdrawal associated exacerbation of OCB. These results indicate that OCB associated with morphine withdrawal state is partly mediated by the activation of central CRF receptors.
机译:最近的研究提供了令人信服的证据,证明阿片类药物成瘾与强迫症(OCD)并存,以及促肾上腺皮质激素释放因子(CRF)参与吗啡戒断的影响。一些不足的证据还指出,CRF在强迫症和相关疾病中的作用。但是,没有证据表明CRF在吗啡戒断相关的强迫行为(OCB)中的作用。因此,本研究调查了CRF在吗啡戒断所致小鼠OCB中的作用。由于该模型具有良好的预测和面部有效性,因此使用了小鼠的大理石掩埋行为来评估OCB。结果表明,急性吗啡剂量依赖性地减弱了大理石的埋藏行为,而慢性吗啡的退出与大理石埋藏行为的显着增加有关。这表明急性吗啡和慢性吗啡戒断对OCB有不同的作用。此外,使用CRF受体拮抗剂(如antalarmin(2和4.μg/小鼠,icv)或astressin-2B(3和10。nmol/小鼠,icv))进行的急性治疗剂量依赖性地减弱了吗啡戒断高峰引起的大理石埋藏行为的增加。 。此外,与antalarmin(4. g /小鼠,静脉内)或astressin-2B(10. nmol /小鼠,静脉内)联合使用吗啡可以阻止吗啡戒断引起的OCB恶化。这些结果表明,与吗啡戒断状态相关的OCB部分由中央CRF受体的激活介导。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号