AMPK is involved in endogenous NO production. A and
B, HUVECs were pretreated with compound C (compC, 20
μm, 30 min) prior to stimulation with SNP (50 μm,
1 h). Cell lysates were subjected to Western blot analysis using antibodies
against phospho-AMPK (Thr-172), AMPK-α, phospho-eNOS (Ser-1177), eNOS,
or β-actin. Typical blots and densitometric analysis (means ±
S.E., n >= 3) are presented. C, PTIO (0.3 mm,
30 min) or A23187 (2μm, 10 min) was added to primary cultured
AMPK-α2 knock-out and WT mouse aorta endothelium cells, and NO
production was measured as described under “Experimental
Procedures.” *, p < 0.05 versus vehicle.