Hansson A L, Nässberger L
Pharmacol Toxicol. 1993 Aug;73(2):75-8. doi: 10.1111/j.1600-0773.1993.tb01539.x.
Autoantibodies directed against myeloperoxidase and elastase have been found in patients developing hydralazine-induced lupus and hydralazine-induced isolated glomerulonephritis. The aim of this study was to investigate influence of hydralazine and dihydralazine upon myeloperoxidase and elastase enzyme activity. Using a 4-aminoantipyrin in vitro system, dihydralazine was 2.5 times as potent in inhibiting myeloperoxidase activity as compared to hydralazine. The corresponding Ki-values were 4 microns M for dihydralazine and 25 microM for hydralazine. When using 2.2'-azino-bis-3-ethyl-benzothiazoline-6-sulphonic acid system inhibition was found at lower concentrations. Furthermore, the difference between the compounds was not so pronounced as seen for 4-aminoantipyrin. The Ki-values for hydralazine and dihydralazine were 1.2 and 1.4 microM respectively. Complete inhibition was seen for both compounds at concentrations above 7.5 microM. Hydralazine binds to elastase, but neither hydralazine nor dihydralazine inhibited elastase enzyme activity.
在发生肼屈嗪诱发的狼疮和肼屈嗪诱发的孤立性肾小球肾炎的患者中,已发现针对髓过氧化物酶和弹性蛋白酶的自身抗体。本研究的目的是调查肼屈嗪和二肼屈嗪对髓过氧化物酶和弹性蛋白酶活性的影响。使用4-氨基安替比林体外系统,与肼屈嗪相比,二肼屈嗪抑制髓过氧化物酶活性的效力是其2.5倍。二肼屈嗪和肼屈嗪的相应Ki值分别为4微摩尔/升和25微摩尔/升。当使用2,2'-联氮-双-3-乙基苯并噻唑啉-6-磺酸系统时,在较低浓度下发现有抑制作用。此外,这两种化合物之间的差异不像在4-氨基安替比林系统中那么明显。肼屈嗪和二肼屈嗪的Ki值分别为1.2微摩尔/升和1.4微摩尔/升。在浓度高于7.5微摩尔/升时,两种化合物均出现完全抑制。肼屈嗪可与弹性蛋白酶结合,但肼屈嗪和二肼屈嗪均未抑制弹性蛋白酶的活性。