SYSTEMIC NITRIC-OXIDE SYNTHASE INHIBITION DOES NOT AFFECT BRAIN OXYGENATION DURING CORTICAL SPREADING DEPRESSION IN RATS - A NONINVASIVE NEAR-INFRARED SPECTROSCOPY AND LASER-DOPPLER FLOWMETRY STUDY
T. Wolf et al., SYSTEMIC NITRIC-OXIDE SYNTHASE INHIBITION DOES NOT AFFECT BRAIN OXYGENATION DURING CORTICAL SPREADING DEPRESSION IN RATS - A NONINVASIVE NEAR-INFRARED SPECTROSCOPY AND LASER-DOPPLER FLOWMETRY STUDY, Journal of cerebral blood flow and metabolism, 16(6), 1996, pp. 1100-1107
Cortical spreading depression (CSD) has been implicated in the migrain
e aura and in stroke. This study demonstrates near-infrared spectrosco
py (NIRS) for the first time as capable of noninvasive on-line detecti
on of CSD in the pentobarbital-anesthetized rat. CSD was accompanied b
y a brief and rapid increase of regional CBF (by laser-Doppler flowmet
ry) to 200-400% baseline. NIRS demonstrates that this hyperperfusion i
s associated with concentration increases of oxyhemoglobin, while deox
yhemoglobin decreases. Simultaneously, oxygen partial pressure, measur
ed on the brain surface with a solid-state polarographic probe, was sh
own to be raised by at least 14 mm HE during CSD. Oxygen-dependent pho
sphorescence life-time quenching measurements confirmed this finding.
NIRS data on cytochrome aa(3), however, showed a CSD-related shift tow
ard a more reduced state, despite raised blood oxygenation. This may s
uggest either limited O-2 transport from the blood to mitochondria or
decreased oxygen utilization during CSD as supposed by theories about
compartmentalization of energy metabolism favoring glycolytic rather t
han aerobic energy supply during CSD. However, the data on cytochrome
aa(3) warrant caution and rue discussed critically. Nitric oxide synth
ase inhibition by systemic application of N'-nitro-L-arginine had no s
ignificant effect on the perfusion response or the tissue Po-2 during
CSD. During most CSD episodes, a brief decrease in MABP by 4-8 mm Hg w
as noted that might be caused by functional decortication during CSD.