Department of Nutritional Sciences, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Mol Nutr Food Res. 2011 Sep;55 Suppl 2:S186-92. doi: 10.1002/mnfr.201100144. Epub 2011 Jul 5.
Molecules involved in skin function are greatly affected by nutritional conditions. However, the mechanism linking high-fat (HF) diets with these alterations is not well understood. This study aimed to investigate the molecular changes in skin function that result from HF diets.
Sprague-Dawley rats were fed HF diets for 28 days. The skin levels of ceramide, lipids and mRNAs involved in lipid metabolism were evaluated using TLC, oil red O staining and quantitative PCR, respectively. The serum adiponectin concentration was determined by ELISA. HF diets led to reduced ceramide levels and lowered skin lipid content. They also decreased mRNA levels of serine palmitoyltransferase (SPT) and 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase in the skin and those of peroxisome proliferator-activated receptor-α -PPAR-α), which upregulates SPT and HMG-CoA reductase expression. The HF diets reduced the serum concentration of adiponectin, which acts upstream of PPAR-α. Finally, these diets led to increased mRNA levels of carnitine palmitoyltransferase-1, the rate-limiting enzyme that acts in β-oxidation.
Our study suggests that HF diets reduce ceramide and lipid synthesis in the skin by reducing levels of SPT and HMG-CoA reductase through lowered adiponectin and PPAR-α activity. Additionally, they decrease lipid content by enhancing β-oxidation.
参与皮肤功能的分子受营养状况的影响很大。然而,将高脂肪(HF)饮食与这些变化联系起来的机制尚不清楚。本研究旨在探讨 HF 饮食导致皮肤功能分子变化的机制。
Sprague-Dawley 大鼠喂食 HF 饮食 28 天。使用薄层色谱法(TLC)、油红 O 染色和定量 PCR 分别评估皮肤中神经酰胺、脂质以及参与脂质代谢的 mRNA 水平。通过 ELISA 测定血清脂联素浓度。HF 饮食导致皮肤中神经酰胺水平降低和皮肤脂质含量降低。它们还降低了皮肤中丝氨酸棕榈酰转移酶(SPT)和 3-羟-3-甲基戊二酰辅酶 A(HMG-CoA)还原酶的 mRNA 水平,这两种酶都上调了 SPT 和 HMG-CoA 还原酶的表达。HF 饮食降低了脂联素的血清浓度,脂联素是 PPAR-α 的上游作用因子。最后,这些饮食导致肉碱棕榈酰基转移酶-1 的 mRNA 水平升高,肉碱棕榈酰基转移酶-1 是β-氧化的限速酶。
我们的研究表明,HF 饮食通过降低脂联素和 PPAR-α 活性降低 SPT 和 HMG-CoA 还原酶的水平,从而减少皮肤中神经酰胺和脂质的合成。此外,它们通过增强β-氧化来降低脂质含量。