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Angiotensin II constricts mouse iliac arteries: possible mechanism for aortic aneurysms

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GADANEC Laura Kate MCSWEENEY Kristen Renee KUBATKA Peter CAPRNDA Martin GASPAR Ludovit PROSECKÝ Robert DRAGASEK Jozef KRUŽLIAK Peter APOSTOLOPOULOS Vasso ZULLI Anthony

Rok publikování 2024
Druh Článek v odborném periodiku
Časopis / Zdroj MOLECULAR AND CELLULAR BIOCHEMISTRY
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://link.springer.com/article/10.1007/s11010-023-04724-0
Doi http://dx.doi.org/10.1007/s11010-023-04724-0
Klíčová slova Abdominal aortic aneurysm; Angiotensin II; Angiotensin type 1 receptor; Angiotensin type 2 receptor; Vasoconstriction
Popis Abdominal aortic aneurysms (AAA) result from maladaptive remodeling of the vascular wall and reduces structural integrity. Angiotensin II (AngII) infusion has become a standard laboratory model for studying AAA initiation and progression. We determined the different vasoactive responses of various mouse arteries to Ang II. Ex vivo isometric tension analysis was conducted on 18-week-old male C57BL/6 mice (n = 4) brachiocephalic arteries (BC), iliac arteries (IL), and abdominal (AA) and thoracic aorta (TA). Arterial rings were mounted between organ hooks, gently stretched and an AngII dose response was performed. Rings were placed in 4% paraformaldehyde for immunohistochemistry analysis to quantify peptide expression of angiotensin type 1 (AT(1)R) and 2 receptors (AT(2)R) in the endothelium, media, and adventitia. Results from this study demonstrated vasoconstriction responses in IL were significantly higher at all AngII doses when compared to BC, and TA and AA responses (maximum constriction-IL: 68.64 +/- 5.47% vs. BC: 1.96 +/- 1.00%; TA: 3.13 +/- 0.16% and AA: 2.75 +/- 1.77%, p < 0.0001). Expression of AT(1)R was highest in the endothelium of IL (p < 0.05) and in the media and (p < 0.05) adventitia (p < 0.05) of AA. In contrast, AT(2)R expression was highest in endothelium (p < 0.05), media (p < 0.01, p < 0.05) and adventitia of TA. These results suggest that mouse arteries display different vasoactive responses to AngII, and the exaggerated response in IL arteries may play a role during AAA development.

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