Bruinink A, Lichtensteiger W
J Recept Res. 1984;4(1-6):127-39. doi: 10.3109/10799898409042544.
The binding of the neuroleptic agent 3H-spiperone and the beta-blocker 3H-dihydroalprenolol (3H-DHA) was investigated in rat forebrain homogenates. The pH of the buffer medium was found to specifically affect binding to certain sites. Omission of ascorbic acid from the binding assay influenced binding in a pH-dependent way. Preincubation with a relatively low concentration of ascorbic acid markedly reduced the binding of both ligands except the nonspecific binding of 3H-spiperone. Lipid peroxidation as revealed by malonyldialdehyde formation, was increased by low and decreased by high ascorbic acid concentrations. The possible relationship between changes in number of binding sites and liposolubility is discussed.
在大鼠前脑匀浆中研究了抗精神病药物3H-螺哌隆和β受体阻滞剂3H-二氢阿普洛尔(3H-DHA)的结合情况。发现缓冲介质的pH值会特异性地影响与某些位点的结合。在结合试验中省略抗坏血酸会以pH依赖的方式影响结合。用相对低浓度的抗坏血酸预孵育会显著降低两种配体的结合,但3H-螺哌隆的非特异性结合除外。由丙二醛形成所揭示的脂质过氧化作用,在低抗坏血酸浓度下增加,在高抗坏血酸浓度下降低。讨论了结合位点数量变化与脂溶性之间的可能关系。