Jagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University, Bobrzynskiego 14, 30-348 Krakow, Poland.
Department of Pharmacology, Medical College, Jagiellonian University, Grzegorzecka 16, 31-531 Krakow, Poland.
Cells. 2021 Jun 22;10(7):1571. doi: 10.3390/cells10071571.
Vitamins K exert a range of activities that extend far beyond coagulation and include anti-inflammatory effects, but the mechanisms involved in anti-inflammatory action remain unclear. In the present study, we showed that various forms of exogenous vitamins-K, K, K (MK-4, MK-5, MK-6 and MK-7)-regulated a wide scope of inflammatory pathways in murine macrophages in vitro, including NOS-2, COX-2, cytokines and MMPs. Moreover, we demonstrated for the first time that macrophages are able to synthesise endogenous MK-4 on their own. Vitamins with shorter isoprenoid chains-K, K and MK-5-exhibited stronger anti-inflammatory potential than vitamins with longer isoprenoid chains (MK-6 and MK-7) and simultaneously were preferably used as a substrate for MK-4 endogenous production. Most interesting, atorvastatin pretreatment inhibited endogenous MK-4 production but had no impact on the anti-inflammatory activity of vitamins K. In summary, our results demonstrate that macrophages are able to synthesise endogenous MK-4 using exogenous vitamins K, and statin inhibits this process. However, the anti-inflammatory effect of exogenous vitamins K was independent of endogenous MK-4 synthesis.
维生素 K 发挥了一系列的作用,远远超出了凝血作用,包括抗炎作用,但抗炎作用的机制仍不清楚。在本研究中,我们表明,各种形式的外源性维生素 K、K、K(MK-4、MK-5、MK-6 和 MK-7)在体外调节了鼠巨噬细胞中广泛的炎症途径,包括 NOS-2、COX-2、细胞因子和 MMPs。此外,我们首次证明巨噬细胞能够自行合成内源性 MK-4。具有较短异戊二烯链的维生素-K、K 和 MK-5-表现出比具有较长异戊二烯链的维生素(MK-6 和 MK-7)更强的抗炎潜力,同时也更适合作为 MK-4 内源性产生的底物。最有趣的是,阿托伐他汀预处理抑制了内源性 MK-4 的产生,但对维生素 K 的抗炎活性没有影响。总之,我们的结果表明,巨噬细胞能够利用外源性维生素 K 合成内源性 MK-4,而他汀类药物抑制了这一过程。然而,外源性维生素 K 的抗炎作用与内源性 MK-4 的合成无关。