Vasopressor peptides and depolarization stimulated Ca 2+-entry into cultured vascular smooth muscle
45Ca-uptake was measured in monolayers of cultured rat aortic smooth muscle cells. Sufficient extracellular 45Ca could be removed by a 90 second cold La 3+ wash to reveal stimulation of 45Ca-uptake by high K +-depolarization and the vasopressor peptides angiotensin II and vasopressin. The high K +-s...
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Published in | Biochemical and biophysical research communications Vol. 148; no. 1; pp. 225 - 231 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
14.10.1987
|
Online Access | Get full text |
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Summary: | 45Ca-uptake was measured in monolayers of cultured rat aortic smooth muscle cells. Sufficient extracellular
45Ca could be removed by a 90 second cold La
3+ wash to reveal stimulation of
45Ca-uptake by high K
+-depolarization and the vasopressor peptides angiotensin II and vasopressin. The high K
+-stimulated
45Ca-influx was blocked by a dihydropyridine-type Ca
2+-antagonist while that stimulated by angiotensin II or vasopressin was not. The
45Ca-influx stimulated by high K
+ - depolarization was additive to that stimulated by angiotensin II. Vasopressin and angiotensin II stimulated
45Ca-fluxes were not additive. It is concluded that vasopressor peptides stimulate Ca
2+-entry through receptor operated Ca
2+-channels which are distinct from voltage gated Ca
2+-channels. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/0006-291X(87)91099-0 |