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NEUROHUMORAL CONTROL OF CARDIOVASCULAR FUNCTION
Department of Pharmacology and Experimental Therapeutics, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois
Submitted 14 September 2005 ; accepted in final form 24 December 2005
5-HT1A-receptor agonists rapidly restore blood pressure and sympathetic activity in conscious rats subjected to hypotensive hemorrhage. 5-HT1A-receptor activation has also been shown to produce a robust increase in baroreceptor-dependent, pulse-synchronous firing of cardiac sympathetic nerves in anesthetized cats. To determine whether 5-HT1A-receptor agonists reverse hemorrhage-induced suppression of sympathetic activity through facilitation of the arterial baroreflex, the effects of the 5-HT1A-receptor agonist, 8-OH-DPAT, were assessed in male Sprague-Dawley rats subjected to sinoaortic baroreceptor denervation and subsequent hypotensive hemorrhage. 8-OH-DPAT produced rapid pressor and sympathoexcitatory responses in hemorrhaged animals that were attenuated, but not blocked, by sinoaortic denervation (SAD) (+49 ± 4 vs. +37 ± 4 mmHg; +165 ± 30 vs. +92 ± 24% baseline, P < 0.01). Spectral analysis of sympathetic activity showed that SAD abolished the 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH-DPAT)-mediated increases in pulse-synchronous (13 ± 1 vs. 5 ± 1% total power for intact vs. SAD rats, P < 0.01) and Mayer wave-related bursting (18 ± 3 vs. 8 ± 1% total power, P < 0.05). However, 8-OH-DPAT continued to increase total power (+72 ± 22 vs. 63 ± 7% prehemorrhage total power, P < 0.05) and power at the respiratory frequency (35 ± 2 vs. 25 ± 4% total power) in SAD animals. These data indicate that full expression of the sympathoexcitatory effect of 8-OH-DPAT requires a functional arterial baroreflex. However, a portion of the effect is due to activation of arterial baroreflex-independent sympathetic pathways.
spectral analysis; 8-hydroxy-2-(di-n-propylamino)-tetralin; Mayer wave; respiration
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