This study investigated the effects of halothane and isoflurane on cGM
P-dependent and independent regulation of vascular contraction of the
isolated rat aorta and on NO-stimulated soluble guanylate cyclase (sGC
) isolated from the perfused rat liver. For the studies of the aorta,
isometric tension of isolated rings, with and without, endothelium was
recorded and cGMP content measured. ACh was used to initiate endothel
ial-dependent relaxation of norepinephrine (NE)-contracted rings while
NO was used to directly stimulate isolated aortic ring sGC which cata
lyzes the isolated aortic ring formation of cGMP. Both halothane and i
soflurane interfered with ACh and NO relaxations and with NO-stimulate
d increases in cGMP. Halothane was more potent, having significant att
enuating effects at 0.34 mM (1 MAC) and 0.72 mM (2 MAC) while isoflura
ne had effects only at 0.53 mM (2 MAC). For the isolated sGC studies,
a soluble liver fraction was prepared from perfused rat livers. In the
absence of NO stimulation, neither halothane nor isoflurane modified
the activity of the sGC. However, during NO-stimulation halothane prod
uced significant, concentration-dependent, inhibition of sGC activity
over a wide range of NO concentrations. Isoflurane also inhibited sGC
activity, but to a lesser extent than halothane. The mechanism whereby
the anesthetics could interfere with sGC from liver and blood vessels
is unknown. It could result from anesthetic interaction at hydrophobi
c sites that may exist in GC. However, the results of both the aorta a
nd liver sGC enzyme studies support the suggestion that these anesthet
ics can compete with NO for its binding site on the ferrous heme of sG
C, with chemical structural differences accounting for the potency var
iations. Both anesthetics also had cGMP independent effects, causing c
oncentration dependent relaxations of NE-contracted vessels without en
dothelium. Isoflurane was about 5 times more effective at 1 MAC than h
alothane. Therefore, the net effects of these anesthetics involve the
sum of two opposite effects on tension of vessels with intact endothel
ium: 1) interference with NO-stimulated cGMP relaxation and 2) direct
stimulation of relaxation (not dependent on changes in cGMP).