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

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F24%3A00079762" target="_blank" >RIV/00159816:_____/24:00079762 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/24:00135112

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s11010-023-04724-0" target="_blank" >https://link.springer.com/article/10.1007/s11010-023-04724-0</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11010-023-04724-0" target="_blank" >10.1007/s11010-023-04724-0</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

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

  • Original language description

    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 &lt; 0.0001). Expression of AT(1)R was highest in the endothelium of IL (p &lt; 0.05) and in the media and (p &lt; 0.05) adventitia (p &lt; 0.05) of AA. In contrast, AT(2)R expression was highest in endothelium (p &lt; 0.05), media (p &lt; 0.01, p &lt; 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.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10601 - Cell biology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Molecular and Cellular Biochemistry

  • ISSN

    0300-8177

  • e-ISSN

    1573-4919

  • Volume of the periodical

    479

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    233-242

  • UT code for WoS article

    000964127200002

  • EID of the result in the Scopus database