دورية أكاديمية

Sildenafil-Induced Revascularization of Rat Hindlimb Involves Arteriogenesis through PI3K/AKT and eNOS Activation

التفاصيل البيبلوغرافية
العنوان: Sildenafil-Induced Revascularization of Rat Hindlimb Involves Arteriogenesis through PI3K/AKT and eNOS Activation
المؤلفون: Baron-Menguy, Celine, Bocquet, Arnaud, Richard, Alexis, Guihot, Anne-Laure, Toutain, Bertrand, Pacaud, Pierre, Fassot, Celine, Loirand, Gervaise, Henrion, Daniel, Loufrani, Laurent
المساهمون: MitoVasc - Physiopathologie Cardiovasculaire et Mitochondriale (MITOVASC), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes), Institut du Thorax Nantes, Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM)
المصدر: ISSN: 1661-6596.
بيانات النشر: HAL CCSD
MDPI
سنة النشر: 2022
مصطلحات موضوعية: remodeling, vasodilation, VEGF, sildenafil, neovascularization, [SDV.MHEP.PHY]Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]
الوصف: International audience ; Hypoxia and inflammation play a major role in revascularization following ischemia. Sildenafil inhibits phosphodiesterase-5, increases intracellular cGMP and induces revascularization through a pathway which remains incompletely understood. Thus, we investigated the effect of sildenafil on post-ischemic revascularization. The left femoral artery was ligated in control and sildenafil-treated (25 mg/kg per day) rats. Vascular density was evaluated and expressed as the left/right leg (L/R) ratio. In control rats, L/R ratio was 33 ± 2% and 54 ± 9%, at 7- and 21-days post-ligation, respectively, and was significantly increased in sildenafil-treated rats to 47 ± 4% and 128 ± 11%, respectively. A neutralizing anti-VEGF antibody significantly decreased vascular density (by 0.48-fold) in control without effect in sildenafil-treated animals. Blood flow and arteriolar density followed the same pattern. In the ischemic leg, HIF-1α and VEGF expression levels increased in control, but not in sildenafil–treated rats, suggesting that sildenafil did not induce angiogenesis. PI3-kinase, Akt and eNOS increased after 7 days, with down-regulation after 21 days. Sildenafil induced outward remodeling or arteriogenesis in mesenteric resistance arteries in association with eNOS protein activation. We conclude that sildenafil treatment increased tissue blood flow and arteriogenesis independently of VEGF, but in association with PI3-kinase, Akt and eNOS activation
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35628350; hal-03814145; https://univ-angers.hal.science/hal-03814145Test; https://univ-angers.hal.science/hal-03814145/documentTest; https://univ-angers.hal.science/hal-03814145/file/ijms-23-05542-v3.pdfTest; PUBMED: 35628350; PUBMEDCENTRAL: PMC9143320
DOI: 10.3390/ijms23105542
الإتاحة: https://doi.org/10.3390/ijms23105542Test
https://univ-angers.hal.science/hal-03814145Test
https://univ-angers.hal.science/hal-03814145/documentTest
https://univ-angers.hal.science/hal-03814145/file/ijms-23-05542-v3.pdfTest
حقوق: http://creativecommons.org/licenses/byTest/ ; info:eu-repo/semantics/OpenAccess
رقم الانضمام: edsbas.1F7C2EE8
قاعدة البيانات: BASE