Acute Effects of Thyroid Hormone on Vascular Smooth Muscle

Thyroid ◽  
1996 ◽  
Vol 6 (5) ◽  
pp. 505-512 ◽  
Author(s):  
KAIE OJAMAA ◽  
JOHN D. KLEMPERER ◽  
IRWIN KLEIN
Keyword(s):  
Smooth Muscle ◽  
Thyroid Hormone ◽  
Vascular Smooth Muscle ◽  
Acute Effects

scholarly journals Thyroid Hormone Activation in Human Vascular Smooth Muscle Cells

2001 ◽  
Vol 88 (3) ◽  
pp. 313-318 ◽  
Author(s):  
Haruo Mizuma ◽  
Masami Murakami ◽  
Masatomo Mori
Keyword(s):  
Smooth Muscle ◽  
Thyroid Hormone ◽  
Vascular Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Vascular Smooth Muscle Cells ◽  
Muscle Cells

scholarly journals Direct, Acute Effects of Klotho and FGF23 on Vascular Smooth Muscle and Endothelium

PLoS ONE ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. e93423 ◽  
Author(s):  
Isabelle Six ◽  
Hirokazu Okazaki ◽  
Priscilla Gross ◽  
Joanna Cagnard ◽  
Cédric Boudot ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Vascular Smooth Muscle ◽  
Acute Effects

scholarly journals Thyroid hormone affects both endothelial and vascular smooth muscle cells in rat arteries

2015 ◽  
Vol 747 ◽  
pp. 18-28 ◽  
Author(s):  
Yin Cai ◽  
Michael M. Manio ◽  
George P.H. Leung ◽  
Aimin Xu ◽  
Eva H.C. Tang ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Thyroid Hormone ◽  
Vascular Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Vascular Smooth Muscle Cells ◽  
Muscle Cells

scholarly journals Thyroid Hormone Targets Matrix Gla Protein Gene Associated With Vascular Smooth Muscle Calcification

2005 ◽  
Vol 97 (6) ◽  
pp. 550-557 ◽  
Author(s):  
Yoji Sato ◽  
Ryo Nakamura ◽  
Mitsutoshi Satoh ◽  
Kayoko Fujishita ◽  
Satoko Mori ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Thyroid Hormone ◽  
Vascular Smooth Muscle ◽  
Protein Gene ◽  
Matrix Gla Protein

Acute effects of cyclosporin and cremophor EL on endothelial function and vascular smooth muscle in the isolated rat heart

1992 ◽  
Vol 6 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Pankaj Mankad ◽  
Jaroslav Spatenka ◽  
Zdenek Slavik ◽  
Gregory O'Neil ◽  
Adrian Chester ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Vascular Smooth Muscle ◽  
Endothelial Function ◽  
Rat Heart ◽  
Isolated Rat Heart ◽  
Cremophor El ◽  
Acute Effects ◽  
Isolated Rat

scholarly journals Thyroid Hormone Activation in Vascular Smooth Muscle Cells Is Negatively Regulated by Glucocorticoid

Thyroid ◽  
2009 ◽  
Vol 19 (7) ◽  
pp. 755-763 ◽  
Author(s):  
Nagaoki Toyoda ◽  
Saori Yasuzawa-Amano ◽  
Emiko Nomura ◽  
Azusa Yamauchi ◽  
Kumiko Nishimura ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Thyroid Hormone ◽  
Vascular Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Vascular Smooth Muscle Cells ◽  
Muscle Cells

Modulation by the steroid/thyroid hormone superfamily of TGF-β-stimulated VEGF release from vascular smooth muscle cells

2006 ◽  
Vol 99 (1) ◽  
pp. 187-195 ◽  
Author(s):  
Kumiko Tanabe ◽  
Haruhiko Tokuda ◽  
Shinji Takai ◽  
Rie Matsushima-Nishiwaki ◽  
Yoshiteru Hanai ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Thyroid Hormone ◽  
Vascular Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Vascular Smooth Muscle Cells ◽  
Muscle Cells ◽  
Vegf Release

Neuronal and Extraneuronal Uptake of 3H-Norepinephrine in the Heart of the Active Bat: An Electron Microscopic Radioautographic Study

1973 ◽  
Vol 31 ◽  
pp. 522-523
Author(s):  
Martin Hagopian ◽  
Michael D. Gershon ◽  
Eladio A. Nunez
Keyword(s):  
Smooth Muscle ◽  
Monoamine Oxidase ◽  
Vascular Smooth Muscle ◽  
Cardiac Muscle ◽  
Maximum Rate ◽  
External Medium ◽  
Extraneuronal Uptake ◽  
Electron Microscopic ◽  
Cardiac Tissues ◽  
High Affinity

The ability of cardiac tissues to take up norepinephrine from an external medium is well known. Two mechanisms, called Uptake and Uptake respectively by Iversen have been differentiated. Uptake is a high affinity system associated with adrenergic neuronal elements. Uptake is a low affinity system, with a higher maximum rate than that of Uptake. Uptake has been associated with extraneuronal tissues such as cardiac muscle, fibroblasts or vascular smooth muscle. At low perfusion concentrations of norepinephrine most of the amine taken up by Uptake is metabolized. In order to study the localization of sites of norepinephrine storage following its uptake in the active bat heart, tritiated norepinephrine (2.5 mCi; 0.064 mg) was given intravenously to 2 bats. Monoamine oxidase had been inhibited with pheniprazine (10 mg/kg) one hour previously to decrease metabolism of norepinephrine.

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