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Departments of Physiology, Pharmacology, and Biochemistry, Center for Perinatal Biology, Loma Linda University School of Medicine, Loma Linda, California 92350
G
protein-regulated Ca2+ sensitivity
of vascular contractile proteins plays an important role in
cerebrovascular reactivity. The present study examines the
intracellular mechanisms that govern G protein-regulated
Ca2+ sensitivity in cerebral
arteries of different size and age. We studied
-escin-permeabilized
segments of common carotid, basilar, and middle cerebral arteries from
nonpregnant adult and near-term fetal sheep. Activation of protein
kinase C (PKC) by (
)-indolactam V or a phorbol ester produced
receptor-independent increases in Ca2+ sensitivity. Such increases
were more marked in immature arteries and were inversely correlated
with artery size in both mature and immature arteries. However,
inhibitors of PKC did not significantly affect increases in
Ca2+ sensitivity in responses to
either serotonin (5-hydroxytryptamine, 5-HT) or guanosine
5'-O-(3-thiotriphosphate)
(GTP
S). Alternatively, deactivation of rho p21, a small G protein
associated with Rho kinase, by exotoxin C3 fully prevented increases in
Ca2+ sensitivity in responses to
5-HT or GTP
S in both adult and fetal arteries of all types. Neither
inhibitors of PKC nor exotoxin C3 altered baseline
Ca2+ sensitivity. We conclude that
patterns of receptor- and/or G protein-mediated modulation of
Ca2+ sensitivity are dependent on
an intracellular pathway that involves activation of small G proteins
and Rho kinase. In contrast, PKC has little, if any, role in
agonist-induced Ca2+ sensitization
under the present experimental conditions.
calcium sensitivity; G proteins; rho p21; maturation; serotonin; sheep
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