Soignier R Denis, Vaccarino Anthony L, Fanti Kostas A, Wilson Aimee M, Zadina James E
Louisiana State University, School of Medicine, 533 Bolivar St., Room 324, New Orleans, LA 70112, USA.
Neurosci Lett. 2004 Aug 12;366(2):211-4. doi: 10.1016/j.neulet.2004.05.046.
The present study examined the development of analgesic tolerance to endomorphin-1 (EM1), endomorphin-2 (EM2), and morphine, and cross-tolerance among these drugs. Male Swiss Webster mice were injected i.c.v. with EM1, EM2, morphine, or vehicle once daily for 5 days, and tested for analgesia in the tail flick test. To determine the extent of cross-tolerance, on the sixth day mice from each of the above groups received i.c.v. injections of EM1, EM2, morphine, or vehicle before analgesic testing. The development of tolerance to EM1 and EM2 closely resembled that of morphine. Complete, symmetrical cross-tolerance was observed between all drugs in the study. These results demonstrate a time-course and extent of tolerance similar to morphine, and support a common mechanism of action through the mu-opioid receptor.
本研究考察了对内吗啡肽 -1(EM1)、内吗啡肽 -2(EM2)和吗啡的镇痛耐受性的发展情况,以及这些药物之间的交叉耐受性。雄性瑞士韦伯斯特小鼠每天经脑室内注射一次EM1、EM2、吗啡或溶剂,持续5天,并在甩尾试验中测试镇痛效果。为了确定交叉耐受性的程度,在第6天,上述每组小鼠在进行镇痛测试前接受脑室内注射EM1、EM2、吗啡或溶剂。对EM1和EM2的耐受性发展与吗啡的耐受性发展非常相似。在该研究中,所有药物之间均观察到完全、对称的交叉耐受性。这些结果证明了与吗啡相似的耐受性时程和程度,并支持通过μ-阿片受体的共同作用机制。