Basu Anandita, Das Anindhya Sundar, Sharma Manoj, Pathak Manash Pratim, Chattopadhyay Pronobesh, Biswas Kaushik, Mukhopadhyay Rupak
Cellular, Molecular and Environmental Biotechnology Laboratory, Department of Molecular Biology and Biotechnology, Tezpur University, Tezpur 784028, Assam, India.
Division of Pharmaceutical Technology, Defense Research Laboratory, Tezpur 784001, Assam, India.
Biochem Biophys Rep. 2017 Aug 26;12:54-61. doi: 10.1016/j.bbrep.2017.08.005. eCollection 2017 Dec.
Cycloxygenase-2 (COX-2) is the inducible isoform of cycloxygenase enzyme family that catalyzes synthesis of inflammatory mediators, prostanoids and prostaglandins, and therefore, can be targeted by anti-inflammatory drugs. Here, we showed a plant polyphenol, kaempferol, attenuated IL-6-induced COX-2 expression in human monocytic THP-1 cells suggesting its beneficial role in chronic inflammation. Kaempferol deactivated and prevented nuclear localization of two major transcription factors STAT3 and NF-κB, mutually responsible for COX-2 induction in response to IL-6. Moreover, STAT3 and NF-κB were simultaneously deactivated by kaempferol in acute inflammation, as shown by carrageenan-induced mouse paw edema model. The concomitant reduction in COX-2 expression in paw tissues suggested kaempferol's role in mitigation of inflammation by targeting STAT3 and NF-κB.
环氧化酶-2(COX-2)是环氧化酶酶家族的诱导型同工酶,可催化炎症介质、前列腺素和前列腺素的合成,因此可作为抗炎药物的作用靶点。在此,我们发现一种植物多酚——山奈酚,可减弱白细胞介素-6(IL-6)诱导的人单核细胞THP-1细胞中COX-2的表达,提示其在慢性炎症中具有有益作用。山奈酚可使两种主要转录因子信号转导子和转录激活子3(STAT3)和核因子κB(NF-κB)失活,并阻止其核定位,这两种转录因子共同负责COX-2对IL-6的诱导反应。此外,如角叉菜胶诱导的小鼠爪肿胀模型所示,在急性炎症中,山奈酚可同时使STAT3和NF-κB失活。爪组织中COX-2表达的同时降低表明山奈酚通过靶向STAT3和NF-κB在减轻炎症中发挥作用。