急性暴露于电场诱导人血浆溶血磷脂酰胆碱(lysoPC)-22:4水平的变化:lysoPC-22:4与TRPV2相互作用对接的分子洞察

Y. Nakagawa-Yagi, H. Hara, H. Nakanishi, T. Tasaka, A. Hara
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引用次数: 3

摘要

使用高压电势(HELP)装置产生电场(EF)的医疗治疗是日本常用的替代疗法。然而,潜在健康益处的潜在机制尚不完全清楚。为了解决这一问题,我们使用选择性反应监测(SRM)分析了健康人在单次HELP暴露(9 kV/电极+ 9 kV/电极,30分钟)前后获得的血浆样本中溶酶型磷脂的水平。溶血磷脂酰胆碱(lysoPC)-22:4在HELP暴露后显著上调。然而,对溶血磷脂酸(lysoPA)或其他lysoPC物种的水平没有影响。LysoPC被认为是瞬时受体电位香草蛋白2 (TRPV2)的内源性激活剂,可以加速肠道运动。我们进一步研究了lysoPC-22:4与TRPV2的硅对接模拟。对接结果表明,lysoPC-22:4具有良好的结合能(-8.2 kcal/mol)。我们的研究结果为EF治疗缓解便秘的分子机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute exposure to an electric field induces changes in human plasma lysophosphatidylcholine (lysoPC)-22:4 levels: Molecular insight into the docking of lysoPC-22:4 interaction with TRPV2
Medical treatment using high-voltage electric potential (HELP) devices to generate an electric field (EF) is an alternative therapy commonly used in Japan. However, the underlying mechanisms of the potential health benefits are not fully understood. To address this issue, we investigated the levels of lyso-form phospholipids using selected reaction monitoring (SRM) analysis in plasma samples obtained from healthy human subjects before and after a single HELP exposure (9 kV/electrode + 9 kV/electrode, 30 min). Lysophosphatidylcholine (lysoPC)-22:4 was significantly upregulated after HELP exposure. However, there was no effect on the levels of lysophosphatidic acid (lysoPA), or other lysoPC species. LysoPC is known to accelerate intestinal movement as a putative endogenous activator of transient receptor potential vanilloid 2 (TRPV2). We further examined the in silico docking simulation of lysoPC-22:4 with TRPV2. Docking results showed that lysoPC-22:4 has good binding energy (-8.2 kcal/mol). Our findings provide new insight into the molecular mechanisms of constipation alleviation by EF therapy.
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