Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Mol Pharm. 2023 Jun 5;20(6):2911-2918. doi: 10.1021/acs.molpharmaceut.2c01053. Epub 2023 Apr 27.
In this study, we investigated the effects of drugs on membrane function in which lipid peroxidation was inhibited by the antioxidant Trolox (TRO) in liposomes containing egg yolk lecithin. Local anesthetics (LAs), such as lidocaine (LID) and dibucaine (DIB), were used as model drugs. The effect of LAs on the inhibitory activity of TRO was evaluated by calculating the p from the inhibition constant calculated by curve fitting. p indicates the strength of TRO membrane protective function. p indicates the strength of LA activity. LAs inhibited lipid peroxidation in a dose-dependent manner and decreased p. The effect of DIB on p was 1.9 times more than that of LID. This result indicated that LA may improve the fluidity of the membrane, which may facilitate the migration of TRO from the membrane to the liquid phase. As a result, TRO is less likely to suppress lipid peroxidation within the lipid membrane, possibly resulting in a decrease in p. The effect of TRO on p was found to be similar in both, indicating that it did not depend on the type of the model drug. These results suggest that our developed procedure successfully quantified the effects of LAs on lipid membrane functions. We were able to obtain the characteristics of model drugs independent of TRO by simultaneously measuring and analyzing the lipid peroxidation inhibitory activities of TRO and model drugs in liposomes.
在这项研究中,我们研究了药物对膜功能的影响,其中脂质过氧化反应被抗氧化剂 Trolox(TRO)抑制,TRO 存在于含有蛋黄卵磷脂的脂质体中。局部麻醉剂(LAs),如利多卡因(LID)和丁卡因(DIB),被用作模型药物。通过计算由曲线拟合得出的抑制常数计算的 p,来评估 LAs 对 TRO 抑制活性的影响。p 表示 TRO 膜保护功能的强度。p 表示 LA 活性的强度。LAs 呈剂量依赖性抑制脂质过氧化反应,并降低 p。DIB 对 p 的影响是 LID 的 1.9 倍。这一结果表明,LA 可能会改善膜的流动性,从而促进 TRO 从膜向液相的迁移。因此,TRO 更不可能抑制脂质膜内的脂质过氧化反应,可能导致 p 降低。TRO 对 p 的影响在两种情况下是相似的,这表明它不依赖于模型药物的类型。这些结果表明,我们开发的程序成功地量化了 LAs 对脂质膜功能的影响。我们能够通过同时测量和分析 TRO 和模型药物在脂质体中的脂质过氧化抑制活性来获得模型药物的特性,而无需依赖 TRO。