Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Jun 15;1087-1088:61-69. doi: 10.1016/j.jchromb.2018.04.029. Epub 2018 Apr 18.
We previously reported that sesame oil (SO) has anti-inflammatory, anti-atherosclerotic and lipid lowering properties in vivo. Our recent studies have shown that, an aqueous extract of sesame oil (SOAE) has also anti-inflammatory and anti-atherosclerotic properties but with no lipid lowering effects. The extent of reduction in atherosclerosis led us to identify components of SOAE and evaluate their anti-inflammatory properties in vitro. Liquid chromatography mass spectrometric method was used to detect and identify components of SOAE. Methoxyphenol derivatives, short and long chain carboxylic acids, dicarboxylic acids, hydroxy and oxo- carboxylic acids were detected. To our surprise, sesamol and its derivatives (lignans), were not present in the SOAE. Among the identified, a combination of methoxy phenol compounds were selected and tested their ability to reduce LPS induced inflammatory gene expression. Monocyte derived macrophages/RAW 264.7 macrophages were pre-treated with these compounds for 2 h, followed by LPS stimulation for 24 h and pro-inflammatory gene expressions were analyzed. These methoxyphenol derivatives showed potent anti-inflammatory properties. In conclusion, the anti-inflammatory molecules associated with SO may contribute the anti-inflammatory and anti-atherosclerotic properties. Also, our results shed light for the development of SOAE based non-pharmacological therapeutics, nutritional supplements and health products for various inflammatory diseases in the future.
我们之前报道过芝麻油(SO)在体内具有抗炎、抗动脉粥样硬化和降血脂的特性。我们最近的研究表明,芝麻油的水提取物(SOAE)也具有抗炎和抗动脉粥样硬化的特性,但没有降血脂的作用。动脉粥样硬化程度的降低促使我们鉴定 SOAE 的成分,并评估其在体外的抗炎特性。采用液相色谱-质谱联用方法检测和鉴定 SOAE 的成分。检测到了甲氧基酚衍生物、短链和长链羧酸、二羧酸、羟基和氧代羧酸。令我们惊讶的是,芝麻油中并不存在芝麻酚及其衍生物(木脂素)。在鉴定出的成分中,选择了一组甲氧基酚化合物,并测试它们降低 LPS 诱导的炎症基因表达的能力。单核细胞衍生的巨噬细胞/RAW264.7 巨噬细胞用这些化合物预处理 2 小时,然后用 LPS 刺激 24 小时,分析促炎基因的表达。这些甲氧基酚衍生物表现出很强的抗炎特性。总之,与 SO 相关的抗炎分子可能有助于其抗炎和抗动脉粥样硬化特性。此外,我们的结果为未来开发基于 SOAE 的非药物治疗、营养补充剂和治疗各种炎症性疾病的保健品提供了思路。