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Department of Physiology, School of Medicine, University of Hiroshima, Hiroshima 734-8551, Japan
The purposes of this study were to investigate
the level of the sympathetic nervous system in which nitric oxide (NO)
mediates regional sympathetic vasoconstriction and to determine whether neural mechanisms are involved in vasoconstriction after NO inhibition. Ganglionic blockade (hexamethonium),
1-receptor blockade (prazosin), and spinal section at T1 were used
to study sympathetic involvement. NO was blocked with
N
-nitro-L-arginine
methyl ester (L-NAME). Regional
blood flow in the mesenteric and renal arteries and terminal aorta was
monitored by electromagnetic flowmetry in conscious rats.
L-NAME (3-5 mg/kg iv)
increased arterial pressure and peripheral resistance. Ganglionic blockade (25 mg/kg iv) significantly reduced the increase in resistance in the mesentery and kidney in intact and spinal-sectioned rats. Ganglionic blockade significantly decreased hindquarter resistance in
intact rats but not in spinal-sectioned rats. Prazosin (200 µg/kg iv)
significantly reduced the increased hindquarter resistance. We
concluded that NO suppresses sympathetic vasoconstriction in the
mesentery and kidney at the spinal level, whereas hindquarter tone is
mediated at supraspinal and synaptic levels.
nitric oxide synthase inhibitor
N
-nitro-L-arginine
methyl ester; mesenteric, renal, and hindquarter tones; spinal
transection; ganglionic blockade;
1-receptor blockade
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