Department of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Department of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA; Integrated Biomedical Sciences Graduate Program, College of Graduate Health Sciences, Memphis, TN 38163, USA.
Cell Rep. 2022 Sep 6;40(10):111306. doi: 10.1016/j.celrep.2022.111306.
TRPV4 channel activation in endothelial cells leads to vasodilation, while impairment of TRPV4 activity is implicated in vascular dysfunction. Strategies that increase TRPV4 activity could enhance vasodilation and ameliorate vascular disorders. Here, we show that supplementation with eicosapentaenoic acid (EPA), an ω-3 polyunsaturated fatty acid known to have beneficial cardiovascular effects, increases TRPV4 activity in human endothelial cells of various vascular beds. Mice carrying the C. elegans FAT-1 enzyme, which converts ω-6 to ω-3 polyunsaturated fatty acids, display higher EPA content and increased TRPV4-mediated vasodilation in mesenteric arteries. Likewise, mice fed an EPA-enriched diet exhibit enhanced and prolonged TRPV4-dependent vasodilation in an endothelial cell-specific manner. We also show that EPA supplementation reduces TRPV4 desensitization, which contributes to the prolonged vasodilation. Neutralization of positive charges in the TRPV4 N terminus impairs the effect of EPA on channel desensitization. These findings highlight the beneficial effects of manipulating fatty acid content to enhance TRPV4-mediated vasodilation.
TRPV4 通道在血管内皮细胞中的激活可导致血管舒张,而 TRPV4 活性的损伤与血管功能障碍有关。增加 TRPV4 活性的策略可以增强血管舒张并改善血管紊乱。在这里,我们表明,补充二十碳五烯酸(EPA),一种已知具有有益心血管作用的 ω-3 多不饱和脂肪酸,可增加各种血管床的人内皮细胞中的 TRPV4 活性。携带将 ω-6 转化为 ω-3 多不饱和脂肪酸的线虫 FAT-1 酶的小鼠显示出更高的 EPA 含量和肠系膜动脉中 TRPV4 介导的血管舒张增加。同样,用富含 EPA 的饮食喂养的小鼠表现出以内皮细胞特异性方式增强和延长的 TRPV4 依赖性血管舒张。我们还表明,EPA 补充可减少 TRPV4 的脱敏,这有助于延长血管舒张。TRPV4 N 端正电荷的中和会损害 EPA 对通道脱敏的作用。这些发现强调了操纵脂肪酸含量以增强 TRPV4 介导的血管舒张的有益效果。