Vitamin D deficiency promotes large rupture-prone abdominal aortic aneurysms and cholecalciferol supplementation limits progression of aneurysms in a mouse model

Autor: Susan K. Morton, Corey S. Moran, Jonathan Golledge, Smriti M. Krishna, Joseph V. Moxon, Vianne Nsengiyumva, Michael W. Clarke, Sai Wang Seto
Rok vydání: 2020
Předmět:
0301 basic medicine
Apolipoprotein B
vitamin D
Blood Pressure
sclerostin
030204 cardiovascular system & hematology
Muscle
Smooth
Vascular

chemistry.chemical_compound
0302 clinical medicine
Aorta
Abdominal

Osteopontin
Research Articles
Cholecalciferol
Mice
Knockout

biology
Angiotensin II
General Medicine
Abdominal aortic aneurysm
Up-Regulation
Disease Progression
cardiovascular system
medicine.medical_specialty
Aortic Rupture
Myocytes
Smooth Muscle

vitamin D deficiency
03 medical and health sciences
Apolipoproteins E
Internal medicine
medicine
Vitamin D and neurology
Animals
Humans
Adaptor Proteins
Signal Transducing

Caloric Restriction
business.industry
Vitamin D Deficiency
medicine.disease
Mice
Inbred C57BL

Disease Models
Animal

030104 developmental biology
Endocrinology
Gene Expression Regulation
chemistry
Cardiovascular System & Vascular Biology
Dietary Supplements
biology.protein
Sclerostin
business
Ex vivo
Aortic Aneurysm
Abdominal
Zdroj: Clinical Science (London, England : 1979)
ISSN: 1470-8736
0143-5221
Popis: Vitamin D deficiency has been associated with human abdominal aortic aneurysm (AAA); however, its role in AAA pathogenesis is unclear. The aim of the present study was to investigate the effect of vitamin D deficiency on AAA development and examine if administering cholecalciferol (CCF) could limit growth of established AAA within the angiotensin-II (AngII) infused apolipoprotein E-deficient mouse model. Mice were rendered vitamin D deficiency through dietary restriction and during AngII infusion developed larger AAAs as assessed by ultrasound and ex vivo morphometry that ruptured more commonly (48% vs. 19%; P=0.028) than controls. Vitamin D deficiency was associated with increased aortic expression of osteopontin and matrix metalloproteinase-2 and -9 than controls. CCF administration to mice with established aortic aneurysms limited AAA growth as assessed by ultrasound (P
Databáze: OpenAIRE