Changes in motoric, exploratory and emotional behaviours and neuronal acetylcholine content and 5-HT turnover in histidine decarboxylase-KO mice

被引:73
作者
Dere, E
De Souza-Silva, MA
Spieler, RE
Lin, JS
Ohtsu, H
Haas, HL
Huston, JP [1 ]
机构
[1] Univ Dusseldorf, Inst Physiol Psychol, Ctr Biol & Med Res, D-40225 Dusseldorf, Germany
[2] Nova SE Univ, Oceanog Ctr, Ft Lauderdale, FL 33314 USA
[3] Univ Lyon 1, INSERM U628, IFR19, Dept Med Expt,Fac Med, F-69373 Lyon, France
[4] Tohoku Univ, Sch Med, Dept Cellular Pharmacol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[5] Univ Dusseldorf, Inst Neurophysiol, Ctr Biol & Med Res, D-40225 Dusseldorf, Germany
关键词
acetylcholine; arousal; habituation; histamine; knockout;
D O I
10.1111/j.1460-9568.2004.03546.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Histamine has been implicated, inter alia, in mechanisms underlying arousal, exploratory behaviour and emotionality. Here, we investigated behavioural and neurochemical parameters related to these concepts, including open-field activity, rotarod performance and anxiety, as well as brain acetylcholine and 5-HT concentrations of mice deficient for the histidine decarboxylase (HDC) gene. These mice are unable to synthesize histamine from its precursor histidine. The HDC-knockout mice showed reduced exploratory activity in an open-field, but normal habituation to a novel environment. They behaved more anxious than the controls, as assessed by the height-fear task and the graded anxiety test, a modified elevated plus-maze. Furthermore, motor coordination on the rotarod was superior to controls. Biochemical assessments revealed that the HDC-knockout mice had higher acetylcholine concentrations and a significantly higher 5-HT turnover in the frontal cortex, but reduced acetylcholine levels in the neostriatum. These results are suggestive of important interactions between neuronal histamine and these site-specific neurotransmitters, which may be related to the behavioural changes found in the HDC-deficient animals.
引用
收藏
页码:1051 / 1058
页数:8
相关论文
共 52 条
[1]   Pharmacology of sensory stimulation-evoked increases in frontal cortical acetylcholine release [J].
Acquas, E ;
Wilson, C ;
Fibiger, HC .
NEUROSCIENCE, 1998, 85 (01) :73-83
[2]   HISTAMINE IN DORSAL AND VENTRAL HIPPOCAMPUS .2. EFFECTS OF H-1 AND H-2 HISTAMINE-ANTAGONISTS ON EXPLORATORY-BEHAVIOR IN MALE-RATS [J].
ALVAREZ, EO ;
BANZAN, AM .
PHYSIOLOGY & BEHAVIOR, 1986, 37 (01) :39-45
[3]   Chemical kindling induced by pentylenetetrazol in histamine H1 receptor gene knockout mice (H1 KO), histidine decarboxylasedeficient mice (HDC-/-) and mast cell-deficient W/Wv mice [J].
Chen, Z ;
Li, ZY ;
Sakurai, E ;
Mobarakeh, JI ;
Ohtsu, H ;
Watanabe, T ;
Watanabe, T ;
Inuma, K ;
Yanai, K .
BRAIN RESEARCH, 2003, 968 (01) :162-166
[4]   Histamine and spontaneous motor activity: Biphasic changes, receptors involved and participation of the striatal dopamine system [J].
Chiavegatto, S ;
Nasello, AG ;
Bernardi, MM .
LIFE SCIENCES, 1998, 62 (20) :1875-1888
[5]   THIOPERAMIDE, THE SELECTIVE HISTAMINE-H-3 RECEPTOR ANTAGONIST, ATTENUATES STIMULANT-INDUCED LOCOMOTOR-ACTIVITY IN THE MOUSE [J].
CLAPHAM, J ;
KILPATRICK, GJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 259 (02) :107-114
[6]   The anxiolytic-like properties of two selective MAOIs, moclobemide and selegiline, in a standard and an enhanced light/dark aversion test [J].
De Angelis, L ;
Furlan, C .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 65 (04) :649-653
[7]   Histidine-decarboxylase knockout mice show deficient nonreinforced episodic object memory, improved negatively reinforced water-maze performance, and increased neo- and ventro-striatal dopamine turnover [J].
Dere, E ;
De Souza-Silva, MA ;
Topic, B ;
Spieler, RE ;
Haas, HL ;
Huston, JP .
LEARNING & MEMORY, 2003, 10 (06) :510-519
[8]   The graded anxiety test: a novel test of murine unconditioned anxiety based on the principles of the elevated plus-maze and light-dark test [J].
Dere, E ;
Topic, B ;
Silva, MAD ;
Srejic, M ;
Frisch, C ;
Buddenberg, T ;
Huston, JP .
JOURNAL OF NEUROSCIENCE METHODS, 2002, 122 (01) :65-73
[9]  
DICHIARA G, 1991, MESOLIMBIC DOPAMINE SYSTEM : FROM MOTIVATION TO ACTION, P367
[10]   Histaminergic facilitation of electrocorticographic activation: role of basal forebrain, thalamus, and neocortex [J].
Dringenberg, HC ;
Kuo, MC .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 18 (08) :2285-2291