AT1受容体拮抗薬によるメタボリックシンドロームラットの動脈拡張能低下の改善は動脈周囲脂肪組織を介する調節機構に依存しない
Perivascular adipose tissue (PVAT) regulates vascular tone. We demonstrated that PVAT masks impaired vasodilation in the mesenteric arteries of SHRSP.Z-Leprfa/IzmDmcr rats (SHRSP.ZF) with metabolic syndrome (MetS); however, this enhanced vasodilation caused by PVAT disappears at around 23 weeks (wks...
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Published in | 日本薬理学会年会要旨集 p. 3-P-319 |
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Main Authors | , , , |
Format | Journal Article |
Language | Japanese |
Published |
公益社団法人 日本薬理学会
2020
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Subjects | |
Online Access | Get full text |
ISSN | 2435-4953 |
DOI | 10.1254/jpssuppl.93.0_3-P-319 |
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Abstract | Perivascular adipose tissue (PVAT) regulates vascular tone. We demonstrated that PVAT masks impaired vasodilation in the mesenteric arteries of SHRSP.Z-Leprfa/IzmDmcr rats (SHRSP.ZF) with metabolic syndrome (MetS); however, this enhanced vasodilation caused by PVAT disappears at around 23 weeks (wks) of age. Therefore, we investigated whether an angiotensin II type 1 receptor antagonist, azilsartan, protects against the deterioration in PVAT compensatory vasodilator function that occurs with aging in MetS.SHRSP.ZF rats at 13 wks were orally administered azilsartan once daily for 10 wks. The vasodilation response in the superior-mesenteric arteries was determined in the presence or absence of PVAT, using organ bath methods. Azilsartan preserved both acetylcholine- and sodium nitroprusside-induced vasodilation independent of the presence or absence of PVAT, and did not improve the dysfunction in PVAT-mediated modulation of vascular tone in SHRSP.ZF rats.This study demonstrated that the protective effect of azilsartan is mediated by restoring the endothelium- and vascular smooth muscle-mediated mechanisms, and not by improving PVAT dysfunction in MetS. |
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AbstractList | Perivascular adipose tissue (PVAT) regulates vascular tone. We demonstrated that PVAT masks impaired vasodilation in the mesenteric arteries of SHRSP.Z-Leprfa/IzmDmcr rats (SHRSP.ZF) with metabolic syndrome (MetS); however, this enhanced vasodilation caused by PVAT disappears at around 23 weeks (wks) of age. Therefore, we investigated whether an angiotensin II type 1 receptor antagonist, azilsartan, protects against the deterioration in PVAT compensatory vasodilator function that occurs with aging in MetS.SHRSP.ZF rats at 13 wks were orally administered azilsartan once daily for 10 wks. The vasodilation response in the superior-mesenteric arteries was determined in the presence or absence of PVAT, using organ bath methods. Azilsartan preserved both acetylcholine- and sodium nitroprusside-induced vasodilation independent of the presence or absence of PVAT, and did not improve the dysfunction in PVAT-mediated modulation of vascular tone in SHRSP.ZF rats.This study demonstrated that the protective effect of azilsartan is mediated by restoring the endothelium- and vascular smooth muscle-mediated mechanisms, and not by improving PVAT dysfunction in MetS. |
Author | 島利, 美保 籠田, 智美 麓, 加菜 篠塚, 和正 |
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Title | AT1受容体拮抗薬によるメタボリックシンドロームラットの動脈拡張能低下の改善は動脈周囲脂肪組織を介する調節機構に依存しない |
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