4.7 Article

Effects of Local Anesthetics on Liposomal Membranes Determined by Their Inhibitory Activity of Lipid Peroxidation

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MOLECULAR PHARMACEUTICS
卷 20, 期 6, 页码 2911-2918

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AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.2c01053

关键词

?lipid membrane?; ?local anesthetics?; ?singular value decomposition?; ?lipid peroxidation?; ?antioxidants?

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In this study, the effects of drugs on membrane function were investigated using liposomes containing egg yolk lecithin, where lipid peroxidation was inhibited by the antioxidant Trolox (TRO). Local anesthetics (LAs) lidocaine (LID) and dibucaine (DIB) were used as model drugs to evaluate the inhibitory activity of TRO. The results showed that LAs dose-dependently inhibited lipid peroxidation and decreased TRO's membrane protective function. DIB had a stronger effect on TRO compared to LID, indicating that LA may improve membrane fluidity and reduce TRO's inhibition of lipid peroxidation.
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 pI50 from the inhibition constant K calculated by curve fitting. pI50TRO indicates the strength of TRO membrane protective function. pI50LA indicates the strength of LA activity. LAs inhibited lipid peroxidation in a dose-dependent manner and decreased pI50TRO. The effect of DIB on pI50TRO 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 pI50TRO. The effect of TRO on pI50LA 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.

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