Park Soo-Jin, Im Dong-Soon
College of Pharmacy, Pusan National University, Busan 46241, Korea.
Laboratory of Pharmacology, College of Pharmacy, and Department of Biomedical and Pharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Int J Mol Sci. 2021 May 4;22(9):4865. doi: 10.3390/ijms22094865.
2-Arachidonyl-lysophosphatidylethanolamine, shortly 2-ARA-LPE, is a polyunsaturated lysophosphatidylethanolamine. 2-ARA-LPE has a very long chain arachidonic acid, formed by an ester bond at the -2 position. It has been reported that 2-ARA-LPE has anti-inflammatory effects in a zymosan-induced peritonitis model. However, it's action mechanisms are poorly investigated. Recently, resolution of inflammation is considered to be an active process driven by M2 polarized macrophages. Therefore, we have investigated whether 2-ARA-LPE acts on macrophages for anti-inflammation, whether 2-ARA-LPE modulates macrophage phenotypes to reduce inflammation, and whether 2-ARA-LPE is anti-inflammatory in a carrageenan-induced paw edema model. In mouse peritoneal macrophages, 2-ARA-LPE was found to inhibit lipopolysaccharide (LPS)-induced M1 macrophage polarization, but not induce M2 polarization. 2-ARA-LPE inhibited the inductions of inducible nitric oxide synthase and cyclooxygenase-2 in mouse peritoneal macrophages at the mRNA and protein levels. Furthermore, products of the two genes, nitric oxide and prostaglandin E, were also inhibited by 2-ARA-LPE. However, 1-oleoyl-LPE did not show any activity on the macrophage polarization and inflammatory responses. The anti-inflammatory activity of 2-ARA-LPE was also verified in vivo in a carrageenan-induced paw edema model. 2-ARA-LPE inhibits LPS-induced M1 polarization, which contributes to anti-inflammation and suppresses the carrageenan-induced paw edema in vivo.
2-花生四烯酰基溶血磷脂酰乙醇胺,简称为2-ARA-LPE,是一种多不饱和溶血磷脂酰乙醇胺。2-ARA-LPE具有一条非常长链的花生四烯酸,通过在-2位的酯键形成。据报道,2-ARA-LPE在酵母聚糖诱导的腹膜炎模型中具有抗炎作用。然而,其作用机制研究较少。近来,炎症的消退被认为是由M2极化巨噬细胞驱动的一个主动过程。因此,我们研究了2-ARA-LPE是否作用于巨噬细胞以发挥抗炎作用,2-ARA-LPE是否调节巨噬细胞表型以减轻炎症,以及2-ARA-LPE在角叉菜胶诱导的爪肿胀模型中是否具有抗炎作用。在小鼠腹腔巨噬细胞中,发现2-ARA-LPE可抑制脂多糖(LPS)诱导的M1巨噬细胞极化,但不诱导M2极化。2-ARA-LPE在mRNA和蛋白质水平上抑制小鼠腹腔巨噬细胞中诱导型一氧化氮合酶和环氧化酶-2的诱导。此外,2-ARA-LPE还抑制这两个基因的产物一氧化氮和前列腺素E。然而,1-油酰基-LPE对巨噬细胞极化和炎症反应没有任何活性。2-ARA-LPE的抗炎活性在角叉菜胶诱导的爪肿胀模型体内也得到了验证。2-ARA-LPE抑制LPS诱导的M1极化,这有助于抗炎并在体内抑制角叉菜胶诱导的爪肿胀。