Yang Zhi-Jie, Tang Jing-Shi, Jia Hong
Department of Physiology, School of Medicine, Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, People's Republic of China.
Neurosci Lett. 2002 Aug 9;328(2):141-4. doi: 10.1016/s0304-3940(02)00514-1.
Our previous studies have indicated that the thalamic nucleus submedius (Sm) is involved in modulation of nociception and plays an important role in an endogenous analgesic system (a feedback loop) consisting of spinal cord-Sm-ventrolateral orbital cortex-periaqueductal gray-spinal cord. To investigate whether opioids are involved in this antinociception pathway, the effects of microinjection of morphine and naloxone into the Sm on the nociceptive behavior (agitation) evoked in the formalin test were investigated in the awake rat using an automated movement detection system. The results indicate that a unilateral microinjection of morphine (5 micro g, 0.5 microl) into the Sm suppresses the formalin-induced agitation response, but does not influence spontaneous motor activity, and that the morphine-induced depression can be reversed by microinjection of the opioid receptor antagonist naloxone (1.0 micro g, 0.5 microl) into the same Sm site. The results suggest that opioid receptors in the Sm may be involved in the Sm-mediated depression of persistent inflammatory pain.
我们之前的研究表明,丘脑正中核(Sm)参与伤害感受的调节,并且在由脊髓-Sm-腹外侧眶额皮质-导水管周围灰质-脊髓组成的内源性镇痛系统(反馈回路)中发挥重要作用。为了研究阿片类药物是否参与此抗伤害感受途径,我们使用自动运动检测系统,在清醒大鼠中研究了向Sm内微量注射吗啡和纳洛酮对福尔马林试验中诱发的伤害性行为(躁动)的影响。结果表明,向Sm单侧微量注射吗啡(5微克,0.5微升)可抑制福尔马林诱导的躁动反应,但不影响自发运动活动,并且通过向同一Sm部位微量注射阿片受体拮抗剂纳洛酮(1.0微克,0.5微升)可逆转吗啡诱导的抑制作用。结果表明,Sm中的阿片受体可能参与Sm介导的持续性炎性疼痛抑制。