Kasman G S, Rosenfeld J P
Brain Res. 1986 Sep 24;383(1-2):271-8. doi: 10.1016/0006-8993(86)90025-9.
High-dose microinjections of morphine sulfate (15 micrograms) and (D-Ala2)-Met-enkephalin (30 micrograms) were made into the ventral periaqueductal gray of rats. Consistent with previous reports using lower doses, both opiates produced hypoalgesia for noxious thermal stimuli applied to the upper and lower body. More hypoalgesia was observed on the face than on the hind legs or tail. Current thresholds of aversive reaction to stimulation in the trigeminal subnucleus caudalis were unaffected by microinjection of either opiate. Systemic injections of 6 mg/kg morphine sulfate profoundly inhibited defense responses to peripheral noxious stimuli and significantly elevated aversive reaction thresholds for stimulation in the trigeminal subnucleus caudalis. Aversive reactions to stimulation in the dorsal periaqueductal gray remained unaffected by either microinjected or systemically administered opiates.
向大鼠腹侧导水管周围灰质中微量注射高剂量硫酸吗啡(15微克)和(D-Ala2)-甲硫氨酸脑啡肽(30微克)。与之前使用较低剂量的报告一致,两种阿片类药物均对施加于上半身和下半身的有害热刺激产生痛觉减退。面部观察到的痛觉减退比后腿或尾巴更明显。微量注射任何一种阿片类药物均未影响三叉神经尾侧亚核中对刺激的厌恶反应的电流阈值。全身注射6mg/kg硫酸吗啡可显著抑制对周围有害刺激的防御反应,并显著提高三叉神经尾侧亚核中刺激的厌恶反应阈值。无论是微量注射还是全身给药阿片类药物,对背侧导水管周围灰质中刺激的厌恶反应均未受到影响。