THE PHOSPHORYLATION OF an M(r) 20,000 myosin light chain (MLC(20)) pro
motes the generation of contractile force through actin-myosin adenosi
ne triphosphatase in most agonist-mediated vascular smooth muscle cell
contraction. However, the role of calcium-mediated contractile proces
ses in sustained arterial narrowing after subarachnoid hemorrhage rema
ins unknown. In a femoral artery model of vasospasm, whole blood was a
pplied to arteries in 54 rats for periods of 2 to 10 days; the contral
ateral artery treated with platelet-rich plasma served as matched cont
rol. During the early stage of vasospasm (Days 2-5), in the media of a
rteries exposed to blood, MLC(20) phosphorylation (including diphospho
rylated forms) increased significantly (30-38%; P < 0.05); total media
l MLC(20) during this interval was comparable to that in controls. Aft
er 5 days, however, total MLC(20) decreased markedly (>90%; P < 0.01)
compared with controls; phosphorylated MLC(20) was undetectable during
this interval. MLC(20)-mediated contractile processes may be prominen
t in the early stages of arterial narrowing after subarachnoid hemorrh
age; later stages are associated with the loss of MLC(20) and the poss
ible persistence of arterial narrowing by other mechanisms.