Oj. Kirkeby et al., Cerebral nitric oxide concentration and microcirculation during hypercapnia, hypoxia, and high intracranial pressure in pigs, J CL NEUROS, 7(6), 2000, pp. 531-538
Intracerebral nitric oxide (NO) concentration was measured to establish the
technique and to investigate the response of the NO concentration to CO2 v
ariations, hypoxia, and reduced cerebral perfusion pressure. An intracerebr
al nitric oxide sensor was used in 10 pigs, Cerebral microcirculation was m
easured by laser Doppler flowmetry. Five pigs received 40 mg/kg nitro-1-arg
inine methyl ester (L-NAME), Baseline NO concentration was 246 +/- 42 nM. H
ypercapnia increased cerebral microcirculation (P < 0.05) and NO concentrat
ion (P< 0.05). Hypoxia decreased NO concentration (P < 0.05). During high i
ntracranial pressure, cerebral microcirculation decreased (P < 0.05) before
the NO concentration decreased (P < 0.05), and after normalisation of the
intracranial pressure the NO concentration increased, but more slowly than
the cerebral microcirculation. L-NAME caused a decrease in cerebral microci
rculation (P< 0.05) and NO concentration (P< 0.05) to a new steady state, a
nd L-NAME attenuated the changes in NO concentration after hypoxia (P < 0.0
5) and high intracranial pressure (P< 0.05). In conclusion, the electrochem
ical sensor appears to reliably detect changes in localised intracerebral N
O concentration and seems to be a promising tool for direct measurement of
this chemically unstable substance. (C) 2000 Harcourt Publishers Ltd.