Evonik Operations GmbH, Rodenbacher Chaussee 4, 63457 Hanau, Germany.
Department of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University Jena, Philosophenweg 14, 07743 Jena, Germany.
Nutrients. 2022 May 28;14(11):2265. doi: 10.3390/nu14112265.
Specialized pro-resolving mediators (SPM) have emerged as crucial lipid mediators that confer the inflammation-resolving effects of omega-3 polyunsaturated fatty acids (-3 PUFA). Importantly, SPM biosynthesis is dysfunctional in various conditions, which may explain the inconclusive efficacy data from -3 PUFA interventions. To overcome the limitations of conventional -3 PUFA supplementation strategies, we devised a composition enabling the self-sufficient production of SPM in vivo. strains were fed highly bioavailable -3 PUFA, followed by metabololipidomics analysis and bioinformatic assessment of the microbial genomes. All 48 tested strains fed with the -3 PUFA formulation produced a broad range of SPM and precursors thereof in a strain-specific manner, which may be explained by the CYP102A1 gene polymorphisms that we detected. A pilot study was performed to test if a synbiotic /-3 PUFA formulation increases SPM levels in vivo. Supplementation with a synbiotic capsule product led to significantly increased plasma levels of hydroxy-eicosapentaenoic acids (5-HEPE, 15-HEPE, 18-HEPE) and hydroxy-docosahexaenoic acids (4-HDHA, 7-HDHA) as well as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in healthy humans. To the best of our knowledge, we report here for the first time the development and in vivo application of a self-sufficient SPM-producing formulation. Further investigations are warranted to confirm and expand these findings, which may create a new class of -3 PUFA interventions targeting inflammation resolution.
特异性促解决介质 (SPM) 已成为关键的脂质介质,赋予 ω-3 多不饱和脂肪酸 (-3PUFA) 的抗炎作用。重要的是,在各种情况下 SPM 的生物合成都存在功能障碍,这可能解释了 -3PUFA 干预的疗效数据不一致。为了克服传统 -3PUFA 补充策略的局限性,我们设计了一种能够在体内自主生产 SPM 的组合物。用高生物可利用的 -3PUFA 喂养 菌株,然后进行代谢脂质组学分析和微生物基因组的生物信息学评估。用 -3PUFA 配方喂养的所有 48 株 菌株都以菌株特异性的方式产生广泛的 SPM 及其前体,这可以用我们检测到的 CYP102A1 基因多态性来解释。进行了一项初步研究,以测试共生体/-3PUFA 配方是否能在体内增加 SPM 水平。补充共生体胶囊产品导致健康人体内血浆中羟基二十碳五烯酸 (5-HEPE、15-HEPE、18-HEPE) 和羟基二十二碳六烯酸 (4-HDHA、7-HDHA) 以及二十碳五烯酸 (EPA) 和二十二碳六烯酸 (DHA) 的水平显著增加。据我们所知,我们首次报道了自主生产 SPM 的配方的开发和体内应用。需要进一步的研究来证实和扩展这些发现,这可能会创造一类针对炎症解决的新型 -3PUFA 干预措施。