Division of Immunopharmacolgy, School of Pharmacy, Sungkyunkwan University, Suwon, Kyunggi-do 440-746, Republic of Korea.
Food Chem Toxicol. 2012 Aug;50(8):2792-804. doi: 10.1016/j.fct.2012.05.005. Epub 2012 May 11.
Atherosclerosis is a chronic inflammatory disease associated with increased expression of adhesion molecules in vascular smooth muscle cells (VSMCs). The objective of this study was to examine the in vitro effects of extract from aerial Bulbil of Dioscorea batatas Decne (Db-Ex) on the ability to suppress the expression of adhesion molecules induced by TNF-α. We also identified bioactive components from a methanol extract. VSMCs pre-exposed to Db-Ex (10-100 μg/ml) were stimulated with TNF-α (10 ng/ml). Preincubation of VSMCs for 2 h with Db-Ex dose-dependently inhibited TNF-α-induced adhesion of THP-1 monocytic cells and mRNA and protein expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1). Db-Ex treatment decreased ROS production and the amount of phosphorylated form of p38, ERK, JNK and Akt in TNF-α-stimulated cells, suggesting that Db-Ex inhibits adhesion molecule expression possibly through MAPK and Akt regulation. Db-Ex also suppressed TNF-α-activation NK-κB. This effect was mediated through degradation of IκBα and nuclear translocation of the p65 subunit of NF-κB. These results suggest that Db-Ex inhibits monocyte adhesion and the TNF-α-mediated induction of adhesion molecules in VSMC by downregulating the MAPK/Akt/NF-κB signaling pathway, which may explain the ability of Db-Ex to suppress inflammation within the atherosclerotic lesion.
动脉粥样硬化是一种慢性炎症性疾病,与血管平滑肌细胞(VSMCs)中粘附分子的表达增加有关。本研究旨在研究来自穿山龙块茎(Db-Ex)的提取物在体外抑制 TNF-α诱导的粘附分子表达能力的作用。我们还从甲醇提取物中鉴定出生物活性成分。将 VSMCs 预先用 Db-Ex(10-100μg/ml)孵育,然后用 TNF-α(10ng/ml)刺激。Db-Ex 以剂量依赖性方式预孵育 VSMCs 2 小时,可抑制 TNF-α诱导的 THP-1 单核细胞的粘附以及血管细胞粘附分子-1(VCAM-1)和细胞间粘附分子-1(ICAM-1)的 mRNA 和蛋白表达。Db-Ex 处理可减少 TNF-α刺激细胞中 ROS 的产生和磷酸化形式的 p38、ERK、JNK 和 Akt 的量,表明 Db-Ex 通过 MAPK 和 Akt 调节抑制粘附分子的表达。Db-Ex 还抑制了 TNF-α激活的 NK-κB。这种作用是通过 IκBα的降解和 NF-κB 的 p65 亚单位的核易位介导的。这些结果表明,Db-Ex 通过下调 MAPK/Akt/NF-κB 信号通路抑制单核细胞粘附和 TNF-α介导的 VSMC 粘附分子的诱导,这可能解释了 Db-Ex 抑制动脉粥样硬化病变内炎症的能力。