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. 2015 Aug 14;409(1-2):243–253. doi: 10.1007/s11010-015-2528-6

Table 2.

Effect of dexamethasone (DEX) and mechanical stress on cGMP distribution in cultured rat podocytes

NS—non-stressed cells S—stressed cells
Control +DEX Control +DEX
nmol cGMP/105 cells/15 min
ANP [cGMP]t 89 ± 10 44 ± 5# 70 ± 7* 51 ± 6#
[cGMP]e 16 ± 3 14 ± 3 39 ± 6* 30 ± 1
[cGMP]e (%)
[cGMP]t
18 ± 3 38 ± 5# 52 ± 4* 61 ± 6*
ANP+Ang II [cGMP]t 66 ± 3 57 ± 3 49 ± 7 26 ± 5#*$
[cGMP]e 14 ± 2 19 ± 2 34 ± 3* 15 ± 2#
[cGMP]e (%)
[cGMP]t
21 ± 3 28 ± 4 72 ± 5†* 56 ± 2
SNAP [cGMP]t 20 ± 3 31 ± 2# 11 ± 2* 9 ± 2*
[cGMP]e 8 ± 1 14 ± 7 9 ± 2 7 ± 1*
[cGMP]e (%)
[cGMP]t
34 ± 2 36 ± 7 78 ± 5* 81 ± 4*$

The podocytes cultured in 6-well plates with flexible bottom were mechanically stressed for 24 h with or without (control) 1 μM DEX. ANP, SNAP, and Ang II were added for 15 min as described in Materials and Methods. [cGMP]e—extracellular cGMP, [cGMP]t—total cGMP. Results are presented as means from 3 to 4 independent experiments ±SEM

P < 0.05 versus respective non-stretched cells

#  P < 0.05 versus respective control cells

  P < 0.05 versus respective cells without Ang II

$  P < 0.05 versus respective (ANP + DEX) cells