Analysis of cardiovascular function with mutant mice lacking for single or multiple alpha 1 adrenergic receptor.
| Project/Area Number |
17500296
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Laboratory animal science
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| Research Institution | NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT |
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Principal Investigator |
TANOUE Akito NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT, DEPARTMENT OF PHARMACOLOGY, DIRECTOR, 薬剤治療研究部, 部長 (60301800)
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| Co-Investigator(Kenkyū-buntansha) |
KITAGAWA Yoko NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT, RESEARCHER, 薬剤治療研究部, 流動研究員 (50392494)
HIROYAMA Masami NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT, RESEARCHER, 薬剤治療研究部, 共同研究員 (30392492)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2006: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2005: ¥2,600,000 (Direct Cost: ¥2,600,000)
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| Keywords | α1 adrenergic receptor / blood pressure / knockout mouse / 血圧 / α1アドレナリン受容体 / ノックアウトマウス |
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| Research Abstract |
To study the functional role of individual alpha1-adrenergic (AR) subtypes in blood pressure (BP) regulation, we used mice lacking the alpha1B-AR and/or alpha1D-AR with the same genetic background and further studied their hemodynamic and vasoconstrictive responses. Both the alpha1B-AR knockout and alpha1B-/alpha1D-AR double knockout mice, but not the alpha1A-AR knockout mice, had significantly (p < 0.05) lower levels of basal systolic and mean arterial BP than wild-type mice in non-anesthetized condition, and they showed no significant change in heart rate or in cardiac function, as assessed by echocardiogram. Furthermore, triple knockout of three subtypes showed reduced blood pressure. All mutants showed a significantly (p < 0.05) reduced catecholamine-induced pressor and vasoconstriction responses. It is noteworthy that the infusion of norepinephrine did not elicit any pressor response at all in alpha1B-/alpha1D-AR double knockout mice. In an attempt to further examine alpha1-AR subtype, which is involved in the genesis or maintenance of hypertension, BP after salt loading was monitored by tail-cuff readings and confirmed at the endpoint by direct intra-arterial recording. After salt loading, alpha1B-AR knockout mice developed a comparable level of hypertension to wild-type mice, whereas mice lacking alpha1D-AR had significantly (p < 0.05) attenuated BP and lower levels of circulating catecholamines. Our data indicated that alpha1B-and alpha1D-AR subtypes participate cooperatively in BP regulation ; however, the deletion of the functional alpha1D-AR, not alpha1B-AR, leads to an antihypertensive effect. The study shows differential contributions of alpha1B-and alpha1D-ARs in BP regulation.
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Report
(3 results)
Research Products
(24 results)
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[Journal Article] Two α_1-adrenergic receptor subtypes regulating the vasopressor response have differential roles in blood pressure regulation.2005
Author(s)
Hosoda C, Koshimizu T, Tanoue A, Nasa Y, Oikawa R, Tomabechi T, Fukuda S, Shinoura H, Oshikawa S, Takeo S, Kitamura T, Cotecchia S, Tsujimoto G
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Journal Title
Mol. Pharmacol. 67
Pages: 912-922
Description
「研究成果報告書概要(和文)」より
Related Report
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[Journal Article] Two α1-adrenergic receptor subtypes regulating the vasopressor response have differential roles in blood pressure regulation.2005
Author(s)
Hosoda C, Koshimizu T, Tanoue A, Nasa Y, Oikawa R, Tomabechi T, Fukuda S, Shinoura H, Oshikawa S, Takeo S, Kitamura T, Cotecchia S, Tsujimoto G.
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Journal Title
Mol Pharmacol. 67
Pages: 912-922
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Journal Article] Two α_1-adrenergic receptor subtypes regulating the vasopressor response have differential roles in blood pressure regulation.2005
Author(s)
Hosoda C, Koshimizu T, Tanoue A, Nasa Y, Oikawa R, Tomabechi T, Fukuda S, Shinoura H, Oshikawa S, Takeo S, Kitamura T, Cotecchia S, Tsujimoto G.
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Journal Title
Mol.Pharmacol. 67
Pages: 912-922
Related Report
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