LPA-Induced Thromboxane A2-Mediated Vasoconstriction Is Limited to Poly-Unsaturated Molecular Species in Mouse Aortas

• Published in: International journal of molecular sciences 2024-07, Vol.25 (13), p.6872
• Main Authors: Vén, Krisztina, Besztercei, Balázs, Janovicz, Anna, Karsai, Noémi, Chun, Jerold, Tigyi, Gábor, Benyó, Zoltán, Ruisanchez, Éva
• Format: Article
• Language: English
• Subjects: Animals; Aorta - drug effects; Aorta - metabolism; Atherosclerosis; Calcium - metabolism; Coronary vessels; Endothelial Cells - drug effects; Endothelial Cells - metabolism; Endothelium; Fatty acids; Glycerol; Homeostasis; Hydrocarbons; Ligands; lysophosphatidic acid; lysophosphatidic acid receptor 1; Lysophospholipids - metabolism; Lysophospholipids - pharmacology; Male; Mice; Mice, Inbred C57BL; Plasma; Smooth muscle; thromboxane; Thromboxane A2 - metabolism; vasoconstriction; Vasoconstriction - drug effects; Vasodilation - drug effects
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25136872

We have previously reported that, in aortic rings, 18:1 lysophosphatidic acid (LPA) can induce both vasodilation and vasoconstriction depending on the integrity of the endothelium. The predominant molecular species generated in blood serum are poly-unsaturated LPA species, yet the vascular effects of these species are largely unexplored. We aimed to compare the vasoactive effects of seven naturally occurring LPA species in order to elucidate their potential pathophysiological role in vasculopathies. Vascular tone was measured using myography, and thromboxane A (TXA ) release was detected by ELISA in C57Bl/6 mouse aortas. The Ca -responses to LPA-stimulated primary isolated endothelial cells were measured by Fluo-4 AM imaging. Our results indicate that saturated molecular species of LPA elicit no significant effect on the vascular tone of the aorta. In contrast, all 18 unsaturated carbon-containing (C18) LPAs (18:1, 18:2, 18:3) were effective, with 18:1 LPA being the most potent. However, following inhibition of cyclooxygenase (COX), these LPAs induced similar vasorelaxation, primarily indicating that the vasoconstrictor potency differed among these species. Indeed, C18 LPA evoked a similar Ca -signal in endothelial cells, whereas in endothelium-denuded aortas, the constrictor activity increased with the level of unsaturation, correlating with TXA release in intact aortas. COX inhibition abolished TXA release, and the C18 LPA induced vasoconstriction. In conclusion, polyunsaturated LPA have markedly increased TXA -releasing and vasoconstrictor capacity, implying potential pathophysiological consequences in vasculopathies.