Regulation of the crossbridge cycle in vascular smooth muscle by cAMP signalling

2006 ◽  
Vol 27 (5-7) ◽  
pp. 445-454 ◽  
Author(s):  
G. Pfitzer ◽  
L. T. Lubomirov ◽  
K. Reimann ◽  
H. Gagov ◽  
R. Schubert
2017 ◽  
Vol 35 ◽  
pp. 118-128 ◽  
Author(s):  
M. Belacel-Ouari ◽  
L. Zhang ◽  
F. Hubert ◽  
R. Assaly ◽  
R. Gerbier ◽  
...  

Author(s):  
Martin Hagopian ◽  
Michael D. Gershon ◽  
Eladio A. Nunez

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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