Kiritsy-Roy J A, Chan S K, Iwamoto E T
Life Sci. 1983 Feb 21;32(8):889-93. doi: 10.1016/0024-3205(83)90226-6.
D-ala2-met-sulfoxide5-enkephalinamide, DALA(0), was synthesized by oxidizing the 5-methionine residue of D-ala2-met5-enkephalinamide (DALA). Antinociception was assessed on the hot-plate and catalepsy estimated using an immobility test in rats administered DALA, DALA(0) and morphine intraventricularly. By comparing areas under time-effect curves, DALA(0) was 30 times more antinociceptive and up to 40 times more cataleptogenic than DALA. For comparison, morphine induced one-tenth the antinociception and one-fortieth the immobility caused by DALA(0). These results demonstrate that the opiate activity of DALA is clearly enhanced by oxidation of its terminal methionine.
D-丙氨酸2-甲硫氨酸亚砜5-脑啡肽酰胺(DALA(0))是通过氧化D-丙氨酸2-甲硫氨酸5-脑啡肽酰胺(DALA)的5-甲硫氨酸残基合成的。通过热板法评估痛觉缺失,并在脑室注射DALA、DALA(0)和吗啡的大鼠中使用不动试验估计僵住症。通过比较时间-效应曲线下面积,DALA(0)的镇痛作用比DALA强30倍,致僵作用比DALA高40倍。作为比较,吗啡引起的镇痛作用是DALA(0)的十分之一,引起的不动作用是DALA(0)的四十分之一。这些结果表明,DALA的末端甲硫氨酸氧化明显增强了其阿片样活性。