Drastic increase in nitric oxide content in rat brain under halothane anesthesia revealed by EPR method

被引:29
作者
Sjakste, N [1 ]
Baumane, L [1 ]
Meirena, D [1 ]
Lauberte, L [1 ]
Dzintare, M [1 ]
Kalvins, I [1 ]
机构
[1] Latvian Inst Organ Synth, Biochem Grp, LV-1006 Riga, Latvia
关键词
spin trapping; nitric oxide; anesthetics; halothane;
D O I
10.1016/S0006-2952(99)00281-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A drastic increase in nitric oxide (NO) content was revealed by the EPR method in rat brain cortex and cerebellum under halothane anesthesia. The NO scavenger diethyldithiocarbamate sodium salt (DETC) and ferrous citrate were injected into adult rats 30-60 min before anesthesia. Rats were anesthetized by inhalation of a halothane-oxygen mixture (1%, 1.5%, 2%, or 4%). After different times of anesthesia, rats were decapitated, and brain cortex and cerebellum were dissected, frozen in liquid nitrogen, and subjected to EPR spectroscopy. The concentration of NO was determined from the NO-Fe-DETC radical spectrum. In control animals, NO content in the cerebellum was only 68% of that in the cortex. We observed a rime-dependent increase in NO content in the cortex and cerebellum of rats anesthetized with 1.5% halothane. In brain cortex, the NO level increased to six times that of waking animals after 30 min and remained at this level up to 60 min of anesthesia. In cerebellum the changes were less drastic, the NO level showing only a 2-fold increase. The same effect was produced by 1% and 2% halothane. Ketamine, chloral hydrate, and pentobarbital were used as reference drugs. None of these anesthetics produced effects similar to those of halothane. In ketamine-anesthetized rat brain, the NO content slightly decreased. Pentobarbital and chloral hydrate produced an insignificant increase in NO. Data are discussed in the context of possible interference of halothane in the regulation of nitric oxide synthase activity. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:1955 / 1959
页数:5
相关论文
共 41 条
[1]   Cardiac and regional hemodynamic interactions between halothane and nitric oxide synthase activity in dogs [J].
Chelly, JE ;
Doursout, MF ;
Lechevalier, T ;
Liang, YY ;
Chelly, F ;
Hartley, C ;
Kilbourn, RG .
ANESTHESIOLOGY, 1996, 85 (01) :142-149
[2]   Nitric oxide neurotoxicity [J].
Dawson, VL ;
Dawson, TM .
JOURNAL OF CHEMICAL NEUROANATOMY, 1996, 10 (3-4) :179-190
[3]  
FUJIBAYASHI T, 1994, ACTA ANAESTH SCAND, V38, P413
[4]   ANESTHETIC AGENTS DECREASE THE ACTIVITY OF NITRIC-OXIDE SYNTHASE FROM HUMAN POLYMORPHONUCLEAR LEUKOCYTES [J].
GALLEY, HF ;
NELSON, LR ;
WEBSTER, NR .
BRITISH JOURNAL OF ANAESTHESIA, 1995, 75 (03) :326-329
[5]   NITRIC-OXIDE SIGNALING IN THE CENTRAL-NERVOUS-SYSTEM [J].
GARTHWAITE, J ;
BOULTON, CL .
ANNUAL REVIEW OF PHYSIOLOGY, 1995, 57 :683-706
[6]   ENDOTHELIUM-DEPENDENT CIRCULATORY CONTROL - A MECHANISM FOR THE DIFFERING PERIPHERAL VASCULAR EFFECTS OF ISOFLURANE VERSUS HALOTHANE [J].
GREENBLATT, EP ;
LOEB, AL ;
LONGNECKER, DE .
ANESTHESIOLOGY, 1992, 77 (06) :1178-1185
[7]   DISTRIBUTION OF CEREBRAL BLOOD-FLOW DURING HALOTHANE VERSUS ISOFLURANE ANESTHESIA IN RATS [J].
HANSEN, TD ;
WARNER, DS ;
TODD, MM ;
VUST, LJ ;
TRAWICK, DC .
ANESTHESIOLOGY, 1988, 69 (03) :332-337
[8]   Halothane-induced dilatation of intraparenchymal arterioles in rat brain slices: A comparison to sodium nitroprusside [J].
Harkin, CP ;
Hudetz, AG ;
Schmeling, WT ;
Kampine, JP ;
Farber, NE .
ANESTHESIOLOGY, 1997, 86 (04) :885-894
[9]   EPR CHARACTERIZATION OF MOLECULAR TARGETS FOR NO IN MAMMALIAN-CELLS AND ORGANELLES [J].
HENRY, Y ;
LEPOIVRE, M ;
DRAPIER, JC ;
DUCROCQ, C ;
BOUCHER, JL ;
GUISSANI, A .
FASEB JOURNAL, 1993, 7 (12) :1124-1134
[10]   Appearance of electron spin resonance signals in the interaction of dithiocarbamate-Fe(II) with nitrogen dioxide and nitrite [J].
Hiramoto, K ;
Tomiyama, S ;
Kikugawa, K .
FREE RADICAL RESEARCH, 1997, 27 (05) :505-509