Székely J I, Dunai-Kovács Z, Miglécz E, Polgár K, Török K, Földes J, Váradi A, Bános C, Karczag I, Tolna J
Institute for Drug Research, Budapest, Hungary.
Pol J Pharmacol Pharm. 1987 Sep-Oct;39(5):641-56.
D-Met2, Pro5-enkephalinamide (DMPEA) is an opioid peptide having analgesic activity in animals more potent after intravenous administration than morphine. It is less toxic but in animals it showed a higher dependence capacity than morphine. Besides analgesia DMPEA produces in rodent behavioral symptoms similar to those evoked by morphine or beta-endorphin, resembling the actions of neuroleptica. In human trials DMPEA was found to produce unpleasant sensations, no euphoria, and sometimes even dysphoria. DMPEA increases the serum levels of prolactin, growth hormone and, to a less extent, of TSH. Those effect of DMPEA on pituitary hormones. Finally, the human studies indicated that DMPEA antagonized pain (measured with the submaximum effort tourniquet technique), but did not affect adversely and even improved attention and short-term memory; it had no effect on the long-term memory. As the subjective effects of DMPEA are not pleasant, and no patient desired to obtain another treatment, some optimism as to low habit-forming properties of DMPEA may be justified.
D-蛋氨酸2,脯氨酸5-脑啡肽酰胺(DMPEA)是一种阿片肽,在动物体内静脉注射后具有比吗啡更强的镇痛活性。它的毒性较小,但在动物体内显示出比吗啡更高的成瘾性。除了镇痛作用外,DMPEA在啮齿动物中还会产生类似于吗啡或β-内啡肽所引发的行为症状,类似于抗精神病药物的作用。在人体试验中,发现DMPEA会产生不适感,不会产生欣快感,有时甚至会导致烦躁不安。DMPEA会增加催乳素、生长激素的血清水平,对促甲状腺激素的影响较小。这些是DMPEA对垂体激素的作用。最后,人体研究表明,DMPEA可对抗疼痛(采用次最大用力止血带技术测量),但不会产生不良影响,甚至还能改善注意力和短期记忆;对长期记忆没有影响。由于DMPEA的主观效果不佳,没有患者希望接受另一次治疗,因此可以对DMPEA低成瘾性持一定的乐观态度。