Title of article :
Identification of a polymorphic glutamic acid stretch in the α2b-adrenergic receptor and lack of linkage with essential hypertension
Author/Authors :
Clinton T. Baldwin، نويسنده , , Faina Schwartz، نويسنده , , Jader Baima، نويسنده , , Michael Burzstyn، نويسنده , , Anita L. DeStefano، نويسنده , , Irene Gavras، نويسنده , , Diane E. Handy، نويسنده , , Oscar Joost، نويسنده , , Timothy Martel، نويسنده , , Athanasios Manolis، نويسنده , , Michael Nicolaou، نويسنده , , Margaret Bresnahan، نويسنده , , Lindsay Farrer، نويسنده , , Haralambos Gavras، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1999
Pages :
5
From page :
853
To page :
857
Abstract :
Essential hypertension, a clinically significant elevation in blood pressure with no recognizable cause, is believed to be attributable to the collective effect of genetic predisposing factors in combination with specific environmental factors, such as diet and stress. Of the genetic causes, genes coding for proteins involved in blood pressure regulation, such as the α- and β-adrenergic receptors, are obvious candidates. The α2-adrenergic receptor plays a key role in the sympathetic nervous system by mediating the effects of epinephrine and norepinephrine. To evaluate the potential role between the α2B receptor and essential hypertension, we scanned the α2B-receptor gene for genetic variation in 108 affected sibling pairs. The screening revealed two major forms of the receptor. They differ by the presence of either 9 or 12 glutamic acid residues in the acidic domain of the third cytoplasmic loop of the protein. Investigation of the pattern of this variation in hypertensive sibling pairs suggests that the α2B receptor locus does not contribute substantially to genetic susceptibility for essential hypertension.
Keywords :
Essential hypertension , genetics , a2-adrenergic receptor , sympathetic nervous system.
Journal title :
American Journal of Hypertension
Serial Year :
1999
Journal title :
American Journal of Hypertension
Record number :
647291
Link To Document :
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