PROGRESSION OF VASCULAR FUNCTION AND BLOOD PRESSURE IN A MOUSE MODEL OF KAWASAKI DISEASE

• Published in: Shock (Augusta, Ga.) Vol. 59; no. 1; p. 74
• Main Authors: DelVechio, Mia, Alves, Juliano V, Saiyid, Alina Z, Singh, Shubhnita, Galley, Joseph, Awata, Wanessa M C, Costa, Rafael M, Bruder-Nascimento, Ariane, Bruder-Nascimento, Thiago
• Format: Journal Article
• Language: English
• Published: United States 01.01.2023
• Subjects: Animals; Aorta; Blood Pressure; Candida albicans; Disease Models, Animal; Mice; Mucocutaneous Lymph Node Syndrome - metabolism; Rats; Toll-Like Receptor 4; Vasculitis
• ISSN: 1540-0514
• DOI: 10.1097/SHK.0000000000002026

Kawasaki disease (KD) is a systemic vasculitis of childhood characterized by vascular damage in the acute stage, which can persist into the late stage. The vascular mechanisms in the cardiovascular risk of KD are not fully studied. We investigated the vascular function and blood pressure in a murine model of KD. We used the Candida albicans water-soluble (CAWS) fraction model. Mice were injected with 4 mg CAWS for 5 consecutive days and separated into three groups. Control, CAWS 7 days (C7), and CAWS 28 days (C28). Hearts and arteries were harvested for vascular characterization. Rat aortic smooth muscle cells were used to studies in vitro. C7 presented elevated inflammatory markers in the coronary area and abdominal aortas, whereas C28 showed severe vasculitis. No difference was found in blood pressure parameters. Vascular dysfunction characterized by higher contractility to norepinephrine in C7 and C28 in aortic rings was abolished by blocking nitric oxide (NO), reactive oxygen species, and cyclooxygenase (COX)-derived products. The CAWS complex increased COX2 expression in rat aortic smooth muscle cells, which was prevented by Toll-like receptor 4 antagonist. Our data indicate that the murine model of KD is associated with vascular dysfunction likely dependent on COX-derived products, oxidant properties, and NO bioavailability. Furthermore, vascular smooth muscle cell may present an important role in the genesis of vascular dysfunction and vasculitis via the Toll-like receptor 4 pathway. Finally, the CAWS model seems not to be appropriate to study KD-associated shock. More studies are necessary to understand whether vascular dysfunction and COXs are triggers for vasculitis.