Targeted lipidomics reveals changes in N-acyl serines by acute exposure to an electric field: Molecular insights into the docking of N-18:1 serine interaction with TRPV1 or PPAR-α

Y. Nakagawa-Yagi, H. Hara, T. Ohto, H. Nakanishi, Enzo Kawasaki, Takahiro Yamaguchi, A. Hara
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Abstract

Alternative therapy with medical devices using high-voltage electric potential (HELP) to generate an electric field (EF) is common in Japan. However, the mechanisms underlying potential health benefits of this therapy remain unclear. Therefore, we investigated the effect of HELP exposure (9 kV /electrode + 9 kV/electrode, 30 min) on N-acyl serines (N-acyl SERs) using selected reaction monitoring (SRM) analysis in plasma samples obtained from healthy human subjects before and after a single treatment session. N-18:1 SER, and N-16:0 SER were significantly upregulated following HELP exposure. Under these conditions, HELP exposure did not exert on levels of N-18:0 SER, N-18:2 SER, N-20:4 SER, and N-22:6 SER. Because N-18:1 ethanolamine (N-18:1 EA) is known to activate, transient receptor potential vanilloid 1 (TRPV1) and peroxisome proliferator-activated receptor-alpha (PPAR-α), we further examined an in silico docking simulation with TRPV1 and PPAR-α. The binding energies with TRPV1 were -6.359 and -6.227 kcal/mol for N-18:1 SER and N-18:1 EA, respectively. The binding energies with PPAR-α were -7.366 and -6.956 kcal/mol for N-18:1 SER and N-18:1 EA, respectively. In human HepG2 cells, N-18:1 SER enhanced fatty acid-binding protein 1 (FABP1) mRNA expression. N-18:1 SER-induced FABP1 mRNA expression was sensitive to the PPAR-α antagonist GW6471. Our findings provide new insights into the molecular mechanisms of the health benefits of EF therapy. Abbreviations: ACOX1: peroxisomal acyl-coenzyme A oxidase 1; DSPS: delayed sleep phase syndrome; EC50: half maximal effective concentration; EF: electric field; FA: fatty acid; FABP1: fatty acid-binding protein 1; HELP: high-voltage electric potential; HODE: hydroxyoctadecadienoic acid; IL: interleukin; MSL: multiple benign symmetric lipomatosis; N-18:2 EA: N-linoleoyl ethanolamine; N-18:1 EA: N-oleoyl ethanolamine; N-16:0 EA: N-palmitoyl ethanolamine; N-18:0 EA: Nstearoyl ethanolamine; NF-κB: nuclear factor-kappa B; NLRP3: nodlike receptor protein 3; N-20:4 SER: N-arachidonyl serine; N-22:6 SER: N-docosahexaenoyl serine; N-18:2 SER: N-linoleoyl serine; N-18:1 SER: N-oleoyl serine; N-16:0 SER: N-palmitoyl serine; N-18:0 SER: N-stearoyl serine; PLAAT: phospholipase A/acyltransferase; PLA2: phospholipase A2; PPAR-α: peroxisome proliferator-activated receptoralpha; qRT-PCR: quantitative real-time polymerase chain reaction; SRM: selected reaction monitoring; TLR4: toll-like receptor 4; TRPV1: transient receptor potential vanilloid 1.
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靶向脂质组学揭示了急性暴露于电场时n -酰基丝氨酸的变化:N-18:1丝氨酸与TRPV1或PPAR-α相互作用对接的分子见解
在日本,使用高压电势(HELP)产生电场(EF)的医疗设备进行替代疗法是很常见的。然而,这种疗法潜在的健康益处机制尚不清楚。因此,我们研究了HELP暴露(9 kV/电极+ 9 kV/电极,30分钟)对n -酰基丝氨酸(n -酰基SERs)的影响,使用选择性反应监测(SRM)分析了健康受试者在单次治疗前后的血浆样本。N-18:1 SER和N-16:0 SER在HELP暴露后显著上调。在这些条件下,HELP暴露对N-18:0 SER、N-18:2 SER、N-20:4 SER和N-22:6 SER水平没有影响。由于已知N-18:1乙醇胺(N-18:1 EA)可以激活瞬时受体电位香草样蛋白1 (TRPV1)和过氧化物酶体增殖物激活受体α (PPAR-α),我们进一步研究了TRPV1和PPAR-α的硅对接模拟。N-18:1 SER和N-18:1 EA与TRPV1的结合能分别为-6.359和-6.227 kcal/mol。N-18:1 SER和N-18:1 EA与PPAR-α的结合能分别为-7.366和-6.956 kcal/mol。在人HepG2细胞中,N-18:1 SER增强了脂肪酸结合蛋白1 (FABP1) mRNA的表达。N-18:1 ser诱导的FABP1 mRNA表达对PPAR-α拮抗剂GW6471敏感。我们的发现为EF治疗的健康益处的分子机制提供了新的见解。缩写:ACOX1:过氧化物酶体酰基辅酶A氧化酶1;延迟睡眠阶段综合征;EC50:最大有效浓度的一半;EF:电场;FA:脂肪酸;FABP1:脂肪酸结合蛋白1;HELP:高压电势;羟基十八烯二烯酸;IL:白介素;MSL:多发性良性对称脂肪瘤病;N-18:2 EA: n -亚油基乙醇胺;N-18:1 EA: n -油基乙醇胺;N-16:0 EA: n -棕榈酰乙醇胺;N-18:0 EA:硬脂酰乙醇胺;NF-κB:核因子κB;NLRP3:结节样受体蛋白3;N-20:4 SER: n -花生四烯酰基丝氨酸;N-22:6 SER: n -二十二碳六烯丝氨酸;N-18:2 SER: n -亚麻油酰丝氨酸;N-18:1 SER: n -油酰丝氨酸;N-16:0 SER: n -棕榈酰丝氨酸;N-18:0 SER: n -硬脂酰丝氨酸;PLAAT:磷脂酶A/酰基转移酶;PLA2:磷脂酶A2;PPAR-α:过氧化物酶体增殖物激活受体;qRT-PCR:实时定量聚合酶链反应;SRM:选定反应监测;TLR4: toll样受体4;TRPV1:瞬时受体电位香草素1。
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