Ovariectomy Causes Degeneration of Perivascular Adipose Tissue.
Adipocytes
/ pathology
Adipose Tissue
/ pathology
Animals
Aorta
/ pathology
Aortic Aneurysm, Abdominal
/ etiology
Arteries
/ cytology
Atherosclerosis
/ etiology
Collagen
/ metabolism
Elastin
/ metabolism
Extracellular Matrix
/ metabolism
Female
Matrix Metalloproteinase 9
/ metabolism
Menopause
/ physiology
Ovariectomy
/ adverse effects
Ovary
/ physiology
Rats, Sprague-Dawley
abdominal aortic aneurysm
collagen
elastin
ovariectomy
perivascular adipose tissue
vascular diseases
Journal
Journal of oleo science
ISSN: 1347-3352
Titre abrégé: J Oleo Sci
Pays: Japan
ID NLM: 101175339
Informations de publication
Date de publication:
03 Nov 2021
03 Nov 2021
Historique:
pubmed:
15
10
2021
medline:
20
1
2022
entrez:
14
10
2021
Statut:
ppublish
Résumé
Women are more resistant than men to the development of vascular diseases. However, menopause is a factor leading to deterioration of female vascular integrity, and it is reported that the risk of vascular diseases such as atherosclerosis and abdominal aortic aneurysm is increased in postmenopausal women. Although it is suggested that perivascular adipose tissue (PVAT) is deeply involved in the increased risk of vascular disease development, the effect of menopause on PVAT integrity is unknown. In this study, we aimed to elucidate the effect of menopause on PVAT in ovariectomized (OVX) rats. PVAT was divided into 4 regions based on characteristics. Hypertrophy and increased inflammation of adipocytes in the PVAT were observed in the OVX group, but the effects of OVX were different for each region. OVX induced matrix metalloproteinase (MMP) -9 which degrade extracellular matrix such as elastin and collagen fibers in PVAT. Degeneration of the arterial fibers of the thoracic and abdominal aorta were observed in the OVX group. These results indicate that OVX can cause dysfunction of PVAT which can cause degradation of arterial fibers. Appropriate management of PVAT may play an important role in the prevention and treatment of diseases originating from ovarian hypofunction.
Identifiants
pubmed: 34645749
doi: 10.5650/jos.ess21179
doi:
Substances chimiques
Collagen
9007-34-5
Elastin
9007-58-3
Matrix Metalloproteinase 9
EC 3.4.24.35
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM