Abstract
α1-Adrenergic receptors (α1-ARs) modulate a large number of physiological functions in cardiovascular and noncardiovascular tissues. Because individual members of the α1-AR family (α1A-, α1B-, and α1D-ARs) have overlapping expression profiles in most tissues, elucidation of the precise physiological roles of individual α1-AR subtypes remains a challenging task. To alleviate this constraint, a gene targeting approach has been employed to generate mutant mice lacking one or two α1-AR genes. Recent studies on these mutant mouse strains are discussed in this article, with an emphasis on the role of α1-AR in the central nervous system and lower urinary tracts. These are two major tissues of particular interest for the development of new therapeutic strategies targeted to the α1-ARs. By combining gene targeting techniques with pharmacological tools, the specific roles of α1-AR subtypes could be delineated.
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