Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
33
pubmed:dateCreated
2005-8-15
pubmed:abstractText
Androgen has anabolic effects on cardiac myocytes and has been shown to enhance left ventricular enlargement and function. However, the physiological and patho-physiological roles of androgen in cardiac growth and cardiac stress-induced remodeling remains unclear. We aimed to clarify whether the androgen-nuclear androgen receptor (AR) system contributes to the cardiac growth and angiotensin II (Ang II)-stimulated cardiac remodeling by using systemic AR-null male mice. AR knock-out (ARKO) male mice, at 25 weeks of age, and age-matched wild-type (WT) male mice were treated with or without Ang II stimulation (2.0 mg/kg/day) for 2 weeks. ARKO mice with or without Ang II stimulation showed a significant reduction in the heart-to-body weight ratio compared with those of WT mice. In addition, echocardiographic analysis demonstrated impairments of both the concentric hypertrophic response and left ventricular function in Ang II-stimulated ARKO mice. Western blot analysis of the myocardium revealed that activation of extracellular signal-regulated kinases (ERK) 1/2 and ERK5 by Ang II stimulation were lower in ARKO mice than those of WT mice. Ang II stimulation caused more prominent cardiac fibrosis in ARKO mice than in WT mice with enhanced expression of types I and III collagen and transforming growth factor-beta1 genes and with increased Smad2 activation. These results suggest that, in male mice, the androgen-AR system participates in normal cardiac growth and modulates cardiac adaptive hypertrophy and fibrosis during the process of cardiac remodeling under hypertrophic stress.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Angiotensin II, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 1, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 7, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Androgen, http://linkedlifedata.com/resource/pubmed/chemical/Smad2 Protein, http://linkedlifedata.com/resource/pubmed/chemical/Smad2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Tgfb1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta, http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta1
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
19
pubmed:volume
280
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
29661-6
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15961403-Angiotensin II, pubmed-meshheading:15961403-Animals, pubmed-meshheading:15961403-Blood Pressure, pubmed-meshheading:15961403-Cardiomegaly, pubmed-meshheading:15961403-DNA-Binding Proteins, pubmed-meshheading:15961403-Fibrosis, pubmed-meshheading:15961403-Heart Rate, pubmed-meshheading:15961403-Male, pubmed-meshheading:15961403-Mice, pubmed-meshheading:15961403-Mice, Inbred C57BL, pubmed-meshheading:15961403-Mice, Inbred CBA, pubmed-meshheading:15961403-Mice, Knockout, pubmed-meshheading:15961403-Mitogen-Activated Protein Kinase 1, pubmed-meshheading:15961403-Mitogen-Activated Protein Kinase 3, pubmed-meshheading:15961403-Mitogen-Activated Protein Kinase 7, pubmed-meshheading:15961403-Myocardium, pubmed-meshheading:15961403-RNA, Messenger, pubmed-meshheading:15961403-Receptors, Androgen, pubmed-meshheading:15961403-Smad2 Protein, pubmed-meshheading:15961403-Trans-Activators, pubmed-meshheading:15961403-Transforming Growth Factor beta, pubmed-meshheading:15961403-Transforming Growth Factor beta1, pubmed-meshheading:15961403-Ventricular Remodeling
pubmed:year
2005
pubmed:articleTitle
Androgen receptor gene knockout male mice exhibit impaired cardiac growth and exacerbation of angiotensin II-induced cardiac fibrosis.
pubmed:affiliation
Department of Medicine and Bioregulatory Sciences, Institute of Health Biosciences, The University of Tokushima Graduate School, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't