Pappu A S, Hauser G
Neurochem Res. 1983 Dec;8(12):1565-75. doi: 10.1007/BF00964158.
Propranolol, a cationic amphiphilic drug, caused enhanced incorporation of labeled precursor into phosphatidic acid and its metabolites in rat cerebral cortex mince, suggesting increased biosynthesis or reduced degradation. Inhibition of phosphatidate phosphohydrolase could explain the observed drug-induced accumulation of phosphatidic acid and other acidic lipids. Propranolol exhibited differential effects on the free and membrane-bound forms of phosphatidate phosphohydrolase. The drug inhibited cytoplasmic enzyme in a dose-dependent manner only when membrane-bound substrate was used but had practically no effect on the membrane-bound enzyme irrespective of the nature of the substrate used or on the cytoplasmic enzyme when free substrate was used. Brain cytoplasmic enzyme obtained from rats sacrificed 30 min after intraperitoneal injections of propranolol did not show any inhibition. propranolol bound to membranes may prevent cytoplasmic enzyme action, probably by decreasing the availability of substrate through the formation of stable lipid-drug-protein complexes.
普萘洛尔是一种阳离子两亲性药物,它能使标记前体在大鼠大脑皮层切碎组织中更多地掺入磷脂酸及其代谢产物,这表明生物合成增加或降解减少。磷脂酸磷酸水解酶的抑制作用可以解释所观察到的药物诱导的磷脂酸和其他酸性脂质的积累。普萘洛尔对磷脂酸磷酸水解酶的游离形式和膜结合形式表现出不同的作用。该药物仅在使用膜结合底物时以剂量依赖方式抑制细胞质酶,但无论使用何种底物性质,对膜结合酶实际上都没有影响,当使用游离底物时对细胞质酶也没有影响。腹腔注射普萘洛尔30分钟后处死的大鼠所获得的脑细胞质酶未显示出任何抑制作用。与膜结合的普萘洛尔可能会阻止细胞质酶的作用,可能是通过形成稳定的脂质 - 药物 - 蛋白质复合物来降低底物的可用性。