Abstract
Isolated rat aorta rings, labelled for 10 min with45Ca in control physiological saline solution (PSS), PSS with 10 μM noradrenaline (NA), or 80 mM potassium-PSS (80 K), were washed out into non-labelled, icecold PSS. NA and 80 K increased tissue45Ca. Retention of stimulated45Ca uptake during washout was studied by subtracting the control washout curve from the washout curves of the stimulated tissues. The measured stimulated uptake fell rapidly during the initial 15 min of washout, thereafter decreasing more slowly. These results suggested that a lengthy wash in icecold PSS would lead to an underestimate of stimulated cellular45Ca uptake. The cellular location of the stimulated uptake was confirmed by using diltiazem (10 μM) and forskolin (10 μM) to block specifically the45Ca influxes caused by 80 K and NA, respectively. A similar biphasic loss of stimulated45Ca uptake was seen in icecold lanthanum (50 mM) solution. These data suggest that established methods for measuring cellular Ca in isolated blood vessels may have markedly underestimated the amount of Ca entering cells during stimulation.
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Aaronson, P.I. Estimation of high K- and noradrenaline-induced45Ca uptakes in isolated rat aorta: effects of washing in icecold solutions. Pflugers Arch. 414, 579–583 (1989). https://doi.org/10.1007/BF00580994
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DOI: https://doi.org/10.1007/BF00580994