Altered Cellular Calcium Metabolism in Hypertension: A Reassessment and a Hypothesis

Author(s):  
Massimo Cirillo ◽  
Giovambattista Capasso ◽  
Natale Gaspare De Santo
1989 ◽  
Vol 261 (3) ◽  
pp. 749-754 ◽  
Author(s):  
J Segal ◽  
J Hardiman ◽  
S H Ingbar

We have previously demonstrated that 3,5,3′-tri-iodo-L-thyronine (T3) produces a very rapid and transient increase in calcium uptake and cytoplasmic free calcium concentration in the rat thymocyte, and have postulated that Ca2+-ATPase may contribute to the overall effect of T3 on cellular calcium metabolism. In the present study, we show that in the rat thymocyte, T3 increased plasma membrane Ca2+-ATPase activity. This effect of T3 was very rapid, seen at 30 s after the addition of the hormone, and was concentration-related, evident at a physiological concentration as low as 1 pM. Evaluation of the effect of several thyronine analogues on Ca2+-ATPase activity revealed the following order of potency: D-T3 greater than or equal to 3′-isopropyl-L-T2 = L-T3 = L-T4 = D-T4 greater than L-rT3 greater than 3,5-L-T2 greater than DL-thyronine. Studies with the calmodulin antagonist trifluoperazine demonstrated that thymocyte Ca2+-ATPase activity and its stimulation by T3 are influenced by calmodulin. Other studies showed that several adrenergic agents, agonists and antagonists, had no effect on thymocyte Ca2+-ATPase activity and its stimulation by T3. From these and previous observations, we would suggest that in the rat thymocyte, the T3-induced increase in Ca2+-ATPase activity, which enhances the expulsion of calcium from the cell, plays a role in the diminution and transiency of the stimulatory effect of T3 on thymocyte calcium metabolism.


1978 ◽  
Vol 307 (1 Calcium Trans) ◽  
pp. 391-401 ◽  
Author(s):  
Howard Rasmussen ◽  
Michael C. Gustin

1979 ◽  
Vol 75 (1) ◽  
pp. 91-98
Author(s):  
Chieko KOHDA ◽  
Kazuyo NISHIMURA ◽  
Munekazu GEMBA

1983 ◽  
Vol 98 (5_Part_2) ◽  
pp. 809 ◽  
Author(s):  
HOWARD RASMUSSEN

1968 ◽  
Vol 36 (3) ◽  
pp. 567-582 ◽  
Author(s):  
André Bernard Borle

Calcium metabolism was investigated in HeLa cells. 90% of the calcium of the cell monolayer is bound to an extracellular cell coat and can be removed by trypsin-EDTA. The calcium concentration of the naked cell, freed from its coat, is 0.47 mM. The calcium concentration of the medium does not affect the concentration of the naked cell calcium. However, the calcium of the cell coat is proportional to the calcium concentration in the medium. Calcium uptake into the cell coat increases with increasing calcium concentration of the medium, whereas uptake by the naked cell is independent of the calcium of the medium. Anaerobic conditions and metabolic inhibitors do not inhibit calcium uptake by the cell, a fact suggesting that this transfer is a passive phenomenon. The calcium in the extracellular cell coat, was not affected by parathyroid hormone. In contrast, the hormone increased the cellular calcium concentration by stimulating calcium uptake or by enhancing calcium binding to some cell components. These results suggest that, contrary to current thinking, parathyroid hormone influences the cellular calcium balance by mobilizing calcium from the extracellular fluids in order to increase its concentration in some cellular compartment. It is proposed that these effects can enhance calcium transport.


1991 ◽  
pp. 523-532
Author(s):  
Paul Erne ◽  
Maryse Crabos ◽  
Dieter Engelkamp ◽  
Fritz R. Bühler ◽  
Claus W. Heizmann

Sign in / Sign up

Export Citation Format

Share Document