VASCULAR EFFECTS OF HALOTHANE AND ISOFLURANE - CGMP DEPENDENT AND INDEPENDENT ACTIONS

Citation
M. Jing et al., VASCULAR EFFECTS OF HALOTHANE AND ISOFLURANE - CGMP DEPENDENT AND INDEPENDENT ACTIONS, Life sciences, 56(1), 1994, pp. 19-29
Citations number
25
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
Journal title
ISSN journal
00243205
Volume
56
Issue
1
Year of publication
1994
Pages
19 - 29
Database
ISI
SICI code
0024-3205(1994)56:1<19:VEOHAI>2.0.ZU;2-W
Abstract
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).