Skip to main content
. 2018 Jun 29;315(4):H871–H878. doi: 10.1152/ajpheart.00292.2018

Fig. 1.

Fig. 1.

Removal of extracellular Ca2+ inhibits Ca2+ waves. A–C: typical records of Ca2+ waves recorded in arteriolar smooth muscle cells (SMCs). A: image of a Fluo-4-loaded arteriole with regions of interest (ROIs) used for measuring Ca2+ waves shown on 20 SMCs. The ROIs have been colored and enlarged for display purposes. B: Ca2+ waves recorded in an arteriole in physiological salt solution (PSS) containing 1.8 mM Ca2+ from the 20 ROIs shown in A. C: recordings from 20 ROIs from the same arteriole as in A and B after exposure to nominally Ca2+-free PSS (0 mM Ca2+ PSS). D and E: pseudocolored images of a Fluo-4-loaded arteriole (average projection of a stack of 500 images cropped to show images of the vessels only) in PSS and in 0 mM Ca2+ PSS. F–H: means ± SE (n = 9). F: global Fluo-4 intensity relative to the mean value in PSS (a measure of global myoplasmic Ca2+ concentration). G: diameter. H: occurrence (number of waves/cell), amplitude (F/Fo), and frequency (Hz) of Ca2+ waves in the presence of 1.8 mM Ca2+ (PSS) and after exposure to nominally Ca2+-free PSS (0 mM Ca2+ PSS). *P < 0.05 compared with PSS via paired t-tests. Scale bars in D and E are 20 μm. F, fluorescence intensity; Fo, baseline fluorescence.