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Effect of Glycation Focusing on the Process of Epidermal Lipid Synthesis in a Reconstructed Skin Model and Membrane Fluidity of Stratum Corneum Lipids

Overview
Specialty Endocrinology
Date 2018 Feb 28
PMID 29484088
Citations 2
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Abstract

We previously reported that epidermal glycation causes an increase in saturated fatty acid (FA) content in a differentiated reconstructed skin model and HaCaT cells. However, the relationship between ceramides (CERs) and glycation and their effects on stratum corneum (SC) barrier function was not elucidated. In this study, we investigated the effect of glycation on lipid content in 6-day-old cultured reconstructed skin. We used the EPISKIN RHE 6D model and induced glycation using glyoxal. In addition to transepidermal water loss, content of CERs, cholesterol and FA in the reconstructed epidermal model were analyzed by high performance thin layer chromatography. Expression of genes related to ceramide metabolism was determined by real time RT-PCR. Membrane fluidity of stratum corneum lipid liposomes (SCLL) that mimic glycated epidermis was analyzed using an electron spin resonance technique. It was found that FA was significantly increased by glycation. CER[NS], [AP], and cholesterol were decreased in glycated epidermis. Expression of ceramide synthase 3 () was significantly decreased while fatty acid elongase 3 was increased by glyoxal in a dose dependent manner. Membrane fluidity of SCLL mimicking the lipid composition of glycated epidermis was increased compared with controls. Therefore, disruption of CER and FA content in glycated epidermis may be regulated via expression and contribute to abnormal membrane fluidity.

Citing Articles

The Association between the Level of Advanced Glycation End Products and Objective Skin Quality Parameters.

Martinovic D, Tokic D, Usljebrka M, Lupi-Ferandin S, Cigic L, Vanjaka Rogosic L Life (Basel). 2023; 13(2).

PMID: 36836618 PMC: 9961659. DOI: 10.3390/life13020256.


Advanced Glycation End Products in the Skin: Molecular Mechanisms, Methods of Measurement, and Inhibitory Pathways.

Chen C, Zhang J, Li L, Guo M, He Y, Dong Y Front Med (Lausanne). 2022; 9:837222.

PMID: 35646963 PMC: 9131003. DOI: 10.3389/fmed.2022.837222.

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