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J Cardiovasc Transl Res ; 5(3): 274-9, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22555965

ABSTRACT

Heparan sulfate proteoglycans are abundant matrix and membrane molecules. Smooth muscle specific deletion of one heparan sulfate biosynthetic enzyme, N-deacetylase-N-sulfotransferase1 leads to decreased vascular smooth muscle cell proliferation, and vascular wall thickness. We hypothesized that this may lead to changes in blood pressure in conscious mice. Blood pressure was measured via telemetry in SM22αCre(+)Ndst1(-/-)(n = 4) and wild type (n = 8) mice. Aorta and thoracodorsal artery luminal area is significantly smaller in SM22αCre(+)Ndst1(-/-) (n = 4-8, P = 0.02, P = 0.0002) compared to wild type (n = 7) mice. Diurnal differences were observed in both cohorts for systolic, diastolic, mean arterial blood pressure, and heart rate (P < 0.001 from T test). No significant differences were found in the above parameters between the cohorts in either light or dark times using a linear mixed model. In conclusion, deletion of N-deacetylase-N-sulfotransferase1 in smooth muscle did not influence any of the blood pressure parameters measured despite significant decrease in aorta and thoracodorsal artery luminal area.


Subject(s)
Blood Pressure , Consciousness , Gene Deletion , Muscle, Smooth, Vascular/enzymology , Sulfotransferases/deficiency , Animals , Aorta/enzymology , Blood Pressure Monitoring, Ambulatory , Circadian Rhythm , Genotype , Heart Rate , Integrases/genetics , Linear Models , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Microfilament Proteins/genetics , Muscle Proteins/genetics , Phenotype , Sulfotransferases/genetics , Telemetry , Thoracic Arteries/enzymology , Time Factors
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