Literature DB >> 7631962

Halothane, enflurane, and isoflurane do not affect the basal or agonist-stimulated activity of partially isolated soluble and particulate guanylyl cyclases of rat brain.

Z Zuo1, R A Johns.   

Abstract

BACKGROUND: Evidence suggests that inhalational anesthetics interact with the nitric oxide-guanylyl cyclase signaling pathway in the central nervous system and that the inhibitation of this pathway in brain may result in an anesthetic, analgesic, or sedative effect. The mechanism of the effects inhalational anesthetics on this signaling pathway is not clear. This study attempted to determine whether inhalational anesthetics directly affect soluble or particulate guanylyl cyclase activity in a partially isolated enzyme system.
METHODS: The effects of halothane (0.44-4.4%), enflurane (1.34-6.7%), and isoflurane (0.6-5.0%) on basal or stimulated soluble or particulate guanylyl cyclase activity were examined. Soluble guanylyl cyclase was isolated from whole rat brain and was stimulated by sodium nitroprusside or nitric oxide. Particulate guanylyl cyclase was isolated from rat olfactory bulb and was stimulated by rat atrial natriuretic peptide(1-28). Cyclic guanosine monophosphate content was measured by radiommunoassay. The concentrations of anesthetics in the incubation solution were confirmed by gas chromatography methods.
RESULTS: None of the three anesthetics affected the activity of basal or stimulated soluble or particulate guanylyl cyclase at the concentrations examined in the current experimental conditions.
CONCLUSIONS: These results suggest that halothane, enflurane, and isoflurane do not directly interact with soluble or particulate guanylyl cyclases of rat brain.

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Year:  1995        PMID: 7631962     DOI: 10.1097/00000542-199508000-00020

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  5 in total

1.  Attenuation of nitric oxide-stimulated soluble guanylyl cyclase from the rat brain by halogenated volatile anesthetics.

Authors:  Eiji Masaki; Ichiro Kondo
Journal:  J Anesth       Date:  1998-06       Impact factor: 2.078

2.  Pretreatment with volatile anesthetics, but not with the nonimmobilizer 1,2-dichlorohexafluorocyclobutane, reduced cell injury in rat cerebellar slices after an in vitro simulated ischemia.

Authors:  Chengbin Wang; Jeong Jin Lee; Hae-Hyuk Jung; Zhiyi Zuo
Journal:  Brain Res       Date:  2007-03-15       Impact factor: 3.252

3.  Isoflurane preconditioning reduces mouse microglial activation and injury induced by lipopolysaccharide and interferon-gamma.

Authors:  X Xu; J A Kim; Z Zuo
Journal:  Neuroscience       Date:  2008-04-16       Impact factor: 3.590

4.  Postconditioning with isoflurane reduced ischemia-induced brain injury in rats.

Authors:  Jeong Jin Lee; Liaoliao Li; Hae-Hyuk Jung; Zhiyi Zuo
Journal:  Anesthesiology       Date:  2008-06       Impact factor: 7.892

5.  High-fat diet reduces neuroprotection of isoflurane post-treatment: Role of carboxyl-terminal modulator protein-Akt signaling.

Authors:  Hai Yu; Jiao Deng; Zhiyi Zuo
Journal:  Obesity (Silver Spring)       Date:  2014-08-20       Impact factor: 5.002

  5 in total

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