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The α1D-adrenergic receptor directly regulates arterial blood pressure via vasoconstriction
Akito Tanoue, … , Satoshi Takeo, Gozoh Tsujimoto
Akito Tanoue, … , Satoshi Takeo, Gozoh Tsujimoto
Published March 15, 2002
Citation Information: J Clin Invest. 2002;109(6):765-775. https://doi.org/10.1172/JCI14001.
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Categories: Article Genetics

The α1D-adrenergic receptor directly regulates arterial blood pressure via vasoconstriction

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Abstract

To investigate the physiological role of the α1D-adrenergic receptor (α1D-AR) subtype, we created mice lacking the α1D-AR (α1D–/–) by gene targeting and characterized their cardiovascular function. In α1D–/– mice, the RT-PCR did not detect any transcript of the α1D-AR in any tissue examined, and there was no apparent upregulation of other α1-AR subtypes. Radioligand binding studies showed that α1-AR binding capacity in the aorta was lost, while that in the heart was unaltered in α1D–/– mice. Non-anesthetized α1D–/– mice maintained significantly lower basal systolic and mean arterial blood pressure conditions, relative to wild-type mice, and they showed no significant change in heart rate or in cardiac function, as assessed by echocardiogram. Besides hypotension, the pressor responses to phenylephrine and norepinephrine were decreased by 30–40% in α1D–/– mice. Furthermore, the contractile response of the aorta and the pressor response of isolated perfused mesenteric arterial beds to α1-AR stimulation were markedly reduced in α1D–/– mice. We conclude that the α1D-AR participates directly in sympathetic regulation of systemic blood pressure by vasoconstriction.

Authors

Akito Tanoue, Yoshihisa Nasa, Takaaki Koshimizu, Hitomi Shinoura, Sayuri Oshikawa, Takayuki Kawai, Sachie Sunada, Satoshi Takeo, Gozoh Tsujimoto

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Figure 1

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Generation of α1D-AR–deficient mice. (a) Simplified restriction map arou...
Generation of α1D-AR–deficient mice. (a) Simplified restriction map around exon 1 of the α1D-AR gene and structure of the targeting vector. The coding region of the exon is boxed. Neo, PGK-neo cassette; DT, diphtheria toxin-A fragment gene; B, BamHI; E, EcoRI; EV, EcoRV; H, HindIII; Sa, SalI; SI, SacI; SII, SacII. (b) Southern blot analysis of tail DNA. DNA was digested with EcoRV, and the blot was hybridized with the 3′ probe shown in a. The 7-kb band is derived from the wild-type allele (wild) and the 4-kb band from the targeted allele (mutant).
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