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1 Department of Anesthesiology, Allegheny General Hospital, Pittsburgh, Pennsylvania 15212-4772; and Departments of 2 Neurology and 3 Neurological Surgery, Cleveland Clinic Foundation, Cleveland, Ohio 44195
The maintenance
of constant cerebral blood flow (CBF) as arterial blood pressure is
reduced, commonly referred to as CBF-pressure autoregulation, is
typically characterized by a plateau until the vasodilatory capacity is
exhausted at the lower limit, after which flow falls linearly with
pressure. We investigated the effect of cortical, as opposed to
systemic, nitric oxide synthase (NOS) inhibition on the lower limit of
CBF-pressure autoregulation. Forty-four Sprague-Dawley rats were
anesthetized with halothane and
N2O in
O2. With a closed cranial window
placed the previous day in a ventilated and physiologically stable
preparation, we determined the CBF using laser-Doppler flowmetry.
Animals with low reactivity to inhaled
CO2 and suffused ADP or ACh were
excluded. Five arterial pressures from 100 to 40 mmHg were obtained
with controlled hemorrhagic hypotension under cortical suffusion with artificial cerebrospinal fluid (aCSF) and then again after suffusion for 35 (n = 5) and 105 min
(n = 10) with aCSF,
10
3 M
N
-nitro-L-arginine
(L-NNA;
n = 12), or
10
3 M
N
-nitro-D-arginine
(D-NNA;
n = 5). An additional group
(n = 7) was studied after a 105-min
suffusion of L-NNA followed by a
single blood withdrawal procedure. The lower limit of autoregulation was identified visually by four blinded reviewers as a change in the
slope of the five-point plot of CBF vs. mean arterial blood pressure.
The lower limit of 90 ± 4.3 mmHg after 105 min of 1 mM
L-NNA suffusion was increased
compared with the value in the time-control group of 75 ± 5.3 mmHg
(P < 0.01; ANOVA) and the initial
value of 67 ± 3.7 mmHg (P < 0.001). The lower limit of 84 ± 5.9 mmHg in seven animals with 105 min of suffusion of 1 mM L-NNA
without previous blood withdrawal was significantly increased (P < 0.01) in comparison with 70 ± 1.9 mmHg from those with just aCSF suffusion
(n = 37). No changes in lower limit
for the other agents or conditions, including 105 or 35 min of aCSF or
35 min of L-NNA suffusion, were
detected. The lack of effect on the lower limit with
D-NNA suffusion suggests an
enzymatic mechanism, and the lengthy
L-NNA exposure of 105 min, but
not 35 min, suggests inhibition of a diffusionally distant NOS source
that mediates autoregulation. Thus cortical suffusion of
L-NNA raises the lower limit of
autoregulation, strongly suggesting that nitric oxide is at least one
of the vasodilators active during hypotension as arterial pressure is
reduced from normal.
cerebrovascular circulation; nitric oxide; blood pressure autoregulation; hemorrhagic hypotension; nitric oxide synthase; rats
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