Y. Moritatsuzuki et al., EFFECTS OF NITRIC-OXIDE SYNTHESIS BLOCKADE AND ANGIOTENSIN-II ON BLOOD-FLOW AND SPONTANEOUS VASOMOTION IN THE RAT CEREBRAL MICROCIRCULATION, Acta Physiologica Scandinavica, 148(4), 1993, pp. 449-454
The effects of N(omega)-nitro-L-arginine methyl ester (L-NAME) an inhi
bitor of NO synthesis, or angiotensin II on the frequency and amplitud
e of rhythmic variations (vasomotion) in blood flow of the intact rat
cerebral circulation were investigated using laser-Doppler flowmetry (
LDF). Experiments were performed on Sprague-Dawley rats anaesthetized
with alpha-chloralose. The rat's head was fixed on a stereotaxic frame
and the microvascular blood flow of the parietal cortex on the right
or on both sides was measured via a small hole in the parietal bone, k
eeping the dura and a thin bone layer intact. Following the intravenou
s injection Of L-NAME, the mean arterial blood pressure (MABP) increas
ed to 123 +/- 1 mmHg (1.25 mg kg-1) or to 144 +/- 3 mmHg (5.0 mg kg-1)
but no significant changes in cerebral blood flow (CBF) or vasomotion
could be detected. The observed increase in MABP was sustained until
L-arginine was administered. In the presence Of L-NAME, during stepwis
e reduction of MABP, CBF remained constant when MABP was kept between
60 and 130 mmHg, the vasomotion frequency was lower when MABP was abov
e 80 mmHg but its amplitude was two times higher than in the control g
roup. In another group of animals, angiotensin was infused to give com
parable increments in blood pressure. In contrast to L-NAME, angiotens
in II had no effect on either frequency or amplitude of vasomotion, co
mpared to the control group, within the whole range of MABP studied. O
ur study suggests that NO might be a significant modulator of the micr
ovascular tonus in the brain and that it plays a significant role in c
ontrolling vasomotion frequency and amplitude.