THE TIME-COURSE OF MYOSIN LIGHT-CHAIN PHOSPHORYLATION IN BLOOD-INDUCED VASOSPASM

Citation
T. Harada et al., THE TIME-COURSE OF MYOSIN LIGHT-CHAIN PHOSPHORYLATION IN BLOOD-INDUCED VASOSPASM, Neurosurgery, 36(6), 1995, pp. 1178-1182
Citations number
36
Categorie Soggetti
Surgery,Neurosciences
Journal title
ISSN journal
0148396X
Volume
36
Issue
6
Year of publication
1995
Pages
1178 - 1182
Database
ISI
SICI code
0148-396X(1995)36:6<1178:TTOMLP>2.0.ZU;2-7
Abstract
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.