Wang Hechen, Tian Lu, Han Yiman, Ma Xiaoyao, Hou Yuanyau, Bai Gang
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Tianjin 300353, China.
Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300353, China.
Metabolites. 2022 Jan 27;12(2):121. doi: 10.3390/metabo12020121.
Nonsteroidal anti-inflammatory drugs (NSAIDs), such as cyclooxygenase (Cox)-1/2 inhibitor, have emerged as potent antipyretics and analgesics. However, few herbs with Cox-1/2 inhibitory activity are commonly used for heat-clearing in China. Although these are known to have antipyretic activity, there is a lack of molecular data supporting their activity. Using the traditional Chinese medicine herb honeysuckle (Hon) as an example, we explored key antipyretic active compounds and their mechanisms of action by assessing their metabolites and metabolomics. Mitogen-activated protein kinase (MAPK) 3 and protein kinase B (AKT) 1 were suggested as key targets regulated primarily by chlorogenic acid (CA) and swertiamarin (SWE). CA and SWE synergistically inhibited the production of interleukin (IL)-1 and IL-6, alleviated generation of prostaglandin E2, and played an antipyretic role equivalent to honeysuckle extract at the same dose contents within 3 h. Collectively, these findings indicated that lipopolysaccharide-induced fever can be countered by CA with SWE synergistically, allowing the substitution of a crude extract of complex composition with active compounds. Our findings demonstrated that, unlike the traditional NSAIDs, the Hon extract showed a remote and indirect mechanism for alleviating fever that depended on the phosphatidylinositol-3-kinase-AKT and MAPK pathways by regulating the principal mediator of inflammation.
非甾体抗炎药(NSAIDs),如环氧化酶(Cox)-1/2抑制剂,已成为强效的解热镇痛药。然而,在中国,很少有具有Cox-1/2抑制活性的草药被普遍用于清热。尽管已知这些草药具有解热活性,但缺乏支持其活性的分子数据。以中药金银花(Hon)为例,我们通过评估其代谢产物和代谢组学来探索关键的解热活性化合物及其作用机制。丝裂原活化蛋白激酶(MAPK)3和蛋白激酶B(AKT)1被认为是主要受绿原酸(CA)和獐牙菜苦苷(SWE)调节的关键靶点。CA和SWE协同抑制白细胞介素(IL)-1和IL-6的产生,减轻前列腺素E2的生成,并在3小时内以相同剂量含量发挥与金银花提取物相当的解热作用。总体而言,这些发现表明,CA与SWE协同作用可对抗脂多糖诱导的发热,从而可用活性化合物替代成分复杂的粗提物。我们的研究结果表明,与传统的NSAIDs不同,金银花提取物显示出一种间接的解热机制,该机制依赖于磷脂酰肌醇-3-激酶-AKT和MAPK途径来调节炎症的主要介质。