Neurosurgery · 2002
Role of nitric oxide in the regulation of spinal arteriolar tone.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Ishikawa Mami, Sekizuka Eiichi, Krischek Boris, Sure Ulrich, Becker Ralf, Bertalanffy Helmut
Аннотация
OBJECTIVE: The important role played by nitric oxide (NO) in the maintenance of cerebral arterial tone, both in the resting state and after injury, has been demonstrated, but the role of NO in spinal arteries is unknown. The aim of this study was to verify, by topical application of a NO synthase inhibitor in vivo, the hypothesis that NO plays an important role in the maintenance of spinal arteriolar tone.
METHODS: Closed spinal windows were prepared at the C6 level, for observation of arteriolar reactivity. Male Wistar rats were divided into four groups in the resting state and three groups in the compressed state (which was produced by increasing the intrathecal window pressure). The control group underwent superfusion of artificial cerebrospinal fluid into the spinal window. The nitro-L-arginine-methyl ester (L-NAME) and nitro-D-arginine-methyl ester groups underwent superfusion of the NO synthase inhibitor L-NAME and its inactive enantiomer nitro-d-arginine-methyl ester, respectively. The L-NAME/S-nitroso-acetylpenicillamine (SNAP) group underwent mixed superfusion of L-NAME and the direct NO donor SNAP, for investigation of the effects of an exogenous NO donor.
RESULTS: In the resting state, the arterioles constricted significantly in the L-NAME group, compared with values before L-NAME superfusion and those for the other groups. In the L-NAME/SNAP group, the arterioles dilated significantly after SNAP superfusion, compared with values before superfusion and those for the other groups. In the compressed state, the arterioles dilated after compression in all three groups but the dilation was significantly attenuated in the L-NAME group, compared with values for the control and nitro-D-arginine-methyl ester groups.
CONCLUSION: It is suggested that NO plays an important role in the maintenance of spinal arteriolar tone in the resting and compressed states of the spinal cord.
METHODS: Closed spinal windows were prepared at the C6 level, for observation of arteriolar reactivity. Male Wistar rats were divided into four groups in the resting state and three groups in the compressed state (which was produced by increasing the intrathecal window pressure). The control group underwent superfusion of artificial cerebrospinal fluid into the spinal window. The nitro-L-arginine-methyl ester (L-NAME) and nitro-D-arginine-methyl ester groups underwent superfusion of the NO synthase inhibitor L-NAME and its inactive enantiomer nitro-d-arginine-methyl ester, respectively. The L-NAME/S-nitroso-acetylpenicillamine (SNAP) group underwent mixed superfusion of L-NAME and the direct NO donor SNAP, for investigation of the effects of an exogenous NO donor.
RESULTS: In the resting state, the arterioles constricted significantly in the L-NAME group, compared with values before L-NAME superfusion and those for the other groups. In the L-NAME/SNAP group, the arterioles dilated significantly after SNAP superfusion, compared with values before superfusion and those for the other groups. In the compressed state, the arterioles dilated after compression in all three groups but the dilation was significantly attenuated in the L-NAME group, compared with values for the control and nitro-D-arginine-methyl ester groups.
CONCLUSION: It is suggested that NO plays an important role in the maintenance of spinal arteriolar tone in the resting and compressed states of the spinal cord.