Ondrias K, Stasko A, Jancinová V, Balgavý P
Mol Pharmacol. 1987 Jan;31(1):97-102.
The perturbation effect of the beta-adrenoceptor blocking drugs atenolol, propranolol, practolol, oxprenolol, doberol, pronethanol, metipranolol, alprenolol, Kö-1124, pindolol, and exaprolol on rat brain lipid membrane was investigated by ESR spectroscopy using the spin probe method. Using stearic acids spin labeled at the 5th, 12th, and 16th positions, it was found that lipophilic drugs disorder the membrane and their effect is about 5-10 times higher at the 16th carbon membrane depth than at the 5th depth. Exaprolol induced nonlamellar phases in the bovine brain lipid membrane as detected by 31P NMR spectroscopy. The relative potencies of the drugs at 10 mmol/liter concentration to disorder the lipid membrane at the 16th carbon depth were in the order: exaprolol greater than alprenolol approximately equal to propranolol greater than metipranolol approximately equal to doberol greater than control sample greater than pindolol approximately equal to practolol approximately equal to atenolol. This order qualitatively corresponds with some of their nonspecific biological membrane activities but is not related to their beta-adrenoceptor blocking potencies. The inequality of the membrane perturbation propensities of the drugs indicates that they perturb the lipid membrane in a structure-dependent manner, i.e., that each induces a specific rather than a nonspecific membrane perturbation.
采用自旋探针法,通过电子自旋共振光谱研究了β-肾上腺素能受体阻断药物阿替洛尔、普萘洛尔、普拉洛尔、氧烯洛尔、多贝洛尔、丙萘洛尔、美替洛尔、阿普洛尔、Kö-1124、吲哚洛尔和依沙洛尔对大鼠脑脂质膜的扰动作用。使用在第5、12和16位自旋标记的硬脂酸,发现亲脂性药物会扰乱膜,并且它们在第16个碳膜深度处的作用比在第5个深度处高约5至10倍。通过31P核磁共振光谱检测发现,依沙洛尔在牛脑脂质膜中诱导了非层状相。在10 mmol/L浓度下,这些药物在第16个碳深度处扰乱脂质膜的相对效力顺序为:依沙洛尔>阿普洛尔≈普萘洛尔>美替洛尔≈多贝洛尔>对照样品>吲哚洛尔≈普拉洛尔≈阿替洛尔。该顺序在一定程度上与它们的一些非特异性生物膜活性相对应,但与它们的β-肾上腺素能受体阻断效力无关。药物膜扰动倾向的不平等表明它们以结构依赖的方式扰乱脂质膜,即每种药物诱导的是特定的而非非特异性的膜扰动。