Henningsson S, Persson L, Rosengren E
Biochim Biophys Acta. 1979 Feb 1;582(3):448-57. doi: 10.1016/0304-4165(79)90136-3.
The effects of methylglyoxal bis(guanylhydrazone) on S-adenosyl-L-methionine decarboxylase (EC 4.1.1.50) activity were studied in the mouse kidney stimulated to growth by testosterone administration. The drug was found a potent inhibitor of the enzyme in vitrol Administration of methylglyoxal bis(guanylhydrazone) in vivo resulted in a transient inhibition followed by a strong enhancement of the enzyme activity. Dialysis of the kidney extract, to remove remaining methylglyoxal bis(guanylhydrazone), revealed a great and rapid increase in the activity of S-adenosyl-L-methionine decarboxylase. Injections of testosterone to castrated mice resulted in a marked increase in kidney weight and an accumulation of renal putrescine, spermidine and spermine. These effects of testosterone could not be blocked by simultaneous injections of methylglyoxal bis(guanylhydrazone). It appears that due to secondary effects by which the inhibition of methylglyoxal bis(guanylhydrazone) on S-adenosyl-L-methionine decarboxylase activity is circumvented the inhibitor seems to be of uncertain value in attempts to decrease selectively the in vivo levels of polyamines.
研究了甲基乙二醛双(胍腙)对经睾酮处理刺激生长的小鼠肾脏中S-腺苷-L-甲硫氨酸脱羧酶(EC 4.1.1.50)活性的影响。发现该药物在体外是该酶的有效抑制剂。在体内给予甲基乙二醛双(胍腙)导致短暂抑制,随后酶活性强烈增强。对肾脏提取物进行透析以去除残留的甲基乙二醛双(胍腙),结果显示S-腺苷-L-甲硫氨酸脱羧酶的活性大幅快速增加。给去势小鼠注射睾酮导致肾脏重量显著增加以及肾脏中腐胺、亚精胺和精胺的积累。同时注射甲基乙二醛双(胍腙)不能阻断睾酮的这些作用。看来由于甲基乙二醛双(胍腙)对S-腺苷-L-甲硫氨酸脱羧酶活性的抑制作用被规避的继发效应,该抑制剂在试图选择性降低体内多胺水平的尝试中似乎价值不确定。