Van Rooijen L A, Agranoff B W
Neurochem Res. 1985 Aug;10(8):1019-24. doi: 10.1007/BF00965878.
The calcium-activated phosphodiesteratic hydrolysis of 32P-labeled phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol 4-phosphate in prelabeled nerve ending membranes is inhibited by the aminoglycosides neomycin and gentamicin, and to a lesser extent, by streptomycin. The inhibition is overcome by increasing concentrations of Ca2+, indicating that the aminoglycosides exert their effect by displacing Ca2+ from lipid.
在预先标记的神经末梢膜中,新霉素和庆大霉素这两种氨基糖苷类药物可抑制32P标记的磷脂酰肌醇4,5 - 二磷酸和磷脂酰肌醇4 - 磷酸的钙激活磷酸二酯水解,链霉素的抑制作用较小。增加钙离子浓度可克服这种抑制作用,这表明氨基糖苷类药物通过从脂质中取代钙离子来发挥其作用。