Lee Jae-Won, Kwon Jae-Hyun, Lim Man Sup, Lee Hee Jae, Kim Sung-Soo, Lim So Young, Chun Wanjoo
Department of Pharmacology, College of Medicine, Kangwon National University, Chuncheon, Kangwon, 200-701, Korea.
Mol Cell Biochem. 2014 Dec;397(1-2):109-16. doi: 10.1007/s11010-014-2177-1. Epub 2014 Aug 5.
We previously demonstrated that 3,4,5-trihydorxycinnamic acid (THC), a derivative of hydroxycinnamic acids, possesses protective effect in lipopolysaccharide (LPS)-induced endotoxemia models. However, the effects of THC in LPS-induced septic kidney are still unclear. Therefore, the present study was carried out to examine the effects of THC in LPS-challenged septic kidney using mesangial cell line and Balb/c mice. THC pretreatment effectively inhibited LPS-induced macrophage infiltration and the secretion of pro-inflammatory cytokines in the kidney of LPS-challenged animals. Pretreatment of rat mesangial cells with THC significantly attenuated LPS-induced PGE2 production and COX-2 expression. THC also significantly suppressed LPS-induced expression of MCP-1 in LPS-activated septic kidney and rat mesangial cells. In addition, THC significantly attenuated LPS-induced degradation of IκB-α in LPS-induced rat mesangial cells. THC also increased the expression of heme oxygenase-1 (HO-1) in LPS-challenged septic kidney and mesangial cells. Multiple signaling pathways including p38 and AKT have been observed to be involved in the THC-induced activation of HO-1 expression. The present data clearly demonstrate that THC protects LPS-challenged septic kidney by decreasing macrophage infiltration and increasing HO-1 expression, suggesting that THC might be a valuable therapeutic agent for compromised kidney in sepsis.
我们先前证明,羟基肉桂酸的衍生物3,4,5-三羟基肉桂酸(THC)在脂多糖(LPS)诱导的内毒素血症模型中具有保护作用。然而,THC在LPS诱导的脓毒症肾病中的作用仍不清楚。因此,本研究旨在使用系膜细胞系和Balb/c小鼠来研究THC在LPS攻击的脓毒症肾病中的作用。THC预处理有效抑制了LPS攻击动物肾脏中LPS诱导的巨噬细胞浸润和促炎细胞因子的分泌。用THC预处理大鼠系膜细胞可显著减弱LPS诱导的PGE2产生和COX-2表达。THC还显著抑制了LPS激活的脓毒症肾病和大鼠系膜细胞中LPS诱导的MCP-1表达。此外,THC显著减弱了LPS诱导的大鼠系膜细胞中IκB-α的降解。THC还增加了LPS攻击的脓毒症肾病和系膜细胞中血红素加氧酶-1(HO-1)的表达。已观察到包括p38和AKT在内的多种信号通路参与了THC诱导的HO-1表达激活。目前的数据清楚地表明,THC通过减少巨噬细胞浸润和增加HO-1表达来保护LPS攻击的脓毒症肾病,这表明THC可能是脓毒症中受损肾脏的一种有价值的治疗药物。