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Publication : Heterozygous disruption of activin receptor-like kinase 1 is associated with increased arterial pressure in mice.

First Author  González-Núñez M Year  2015
Journal  Dis Model Mech Volume  8
Issue  11 Pages  1427-39
PubMed ID  26398936 Mgi Jnum  J:226550
Mgi Id  MGI:5697750 Doi  10.1242/dmm.019695
Citation  Gonzalez-Nunez M, et al. (2015) Heterozygous disruption of activin receptor-like kinase 1 is associated with increased arterial pressure in mice. Dis Model Mech 8(11):1427-39
abstractText  The activin receptor-like kinase 1 (ALK-1) is a type I cell-surface receptor for the transforming growth factor-beta (TGF-beta) family of proteins. Hypertension is related to TGF-beta1, because increased TGF-beta1 expression is correlated with an elevation in arterial pressure (AP) and TGF-beta expression is upregulated by the renin-angiotensin-aldosterone system. The purpose of this study was to assess the role of ALK-1 in regulation of AP using Alk1 haploinsufficient mice (Alk1(+/-)). We observed that systolic and diastolic AP were significantly higher in Alk1(+/-) than in Alk1(+/+) mice, and all functional and structural cardiac parameters (echocardiography and electrocardiography) were similar in both groups. Alk1(+/-) mice showed alterations in the circadian rhythm of AP, with higher AP than Alk1(+/+) mice during most of the light period. Higher AP in Alk1(+/-) mice is not a result of a reduction in the NO-dependent vasodilator response or of overactivation of the peripheral renin-angiotensin system. However, intracerebroventricular administration of losartan had a hypotensive effect in Alk1(+/-) and not in Alk1(+/+) mice. Alk1(+/-) mice showed a greater hypotensive response to the beta-adrenergic antagonist atenolol and higher concentrations of epinephrine and norepinephrine in plasma than Alk1(+/+) mice. The number of brain cholinergic neurons in the anterior basal forebrain was reduced in Alk1(+/-) mice. Thus, we concluded that the ALK-1 receptor is involved in the control of AP, and the high AP of Alk1(+/-) mice is explained mainly by the sympathetic overactivation shown by these animals, which is probably related to the decreased number of cholinergic neurons.
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