Interrelations between monoaminergic afferents and corticotropin-releasing factor-immunoreactive neurons in the rat central amygdaloid nucleus: ultrastructural evidence for dopaminergic control of amygdaloid stress systems

被引:33
作者
Eliava, M
Yilmazer-Hanke, D
Asan, E
机构
[1] Univ Wurzburg, Inst Anat & Cell Biol, D-97070 Wurzburg, Germany
[2] Univ Magdeburg, Inst Anat, D-39106 Magdeburg, Germany
关键词
tyrosine hydroxylase; serotonin transporter; dopamine receptors; anxiety; fear;
D O I
10.1007/s00418-003-0557-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ample evidence implicates corticotropin-releasing factor (CRF)-producing neurons of the central amygdaloid nucleus (CeA) in vegetative, endocrine, and behavioral responses to stress and anxiety in laboratory rats. Monoaminergic systems are involved in modulating these responses. In the present paper, interrelations between CRF-immunoreactive (ir) neurons, and noradrenergic, serotonergic, and dopaminergic afferents were studied using single and double immunolabeling for light and electron microscopy in the rat CeA. Dopaminergic axons formed dense plexus in the CeA overlapping with the localization of CRF-ir neurons, and their terminals formed frequent associations with CRF-ir somata. Contacts of serotonergic axons on CRF-ir neurons were few, and contacts of noradrenergic axons were the exception. Ultrastructurally, symmetric synapses of dopaminergic terminals on CRF-ir somata and dendrites were found. More than 83% of CRF-ir somata were contacted in single ultrathin sections. About half of these possessed two or more contacts. Of non-ir somata, 37% were contacted by dopaminergic terminals, and only 13% of these had two or more contacts. Correlative in situ hybridization indicated that CeA CRF-ir neurons may express receptor subtype dopamine receptor subtype 2. In conclusion, dopaminergic afferents appear to specifically target CeA CRF neurons. They are thus in a position to exert significant influence on the rat amygdaloid CRF stress system.
引用
收藏
页码:183 / 197
页数:15
相关论文
共 113 条
[1]   DEPRESSION AS A CONSEQUENCE OF INADEQUATE NEUROCHEMICAL ADAPTATION IN RESPONSE TO STRESSORS [J].
ANISMAN, H ;
ZACHARKO, RM .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 160 :36-43
[2]  
[Anonymous], NEUROANATOMICAL TRAC
[3]  
ASAN E, 1993, HISTOCHEMISTRY, V99, P427
[4]  
Asan E, 1998, Adv Anat Embryol Cell Biol, V142, P1
[5]   QUALITATIVE AND QUANTITATIVE DETECTION OF ALKALINE-PHOSPHATASE COUPLED TO AN OLIGONUCLEOTIDE PROBE FOR SOMATOSTATIN MESSENGER-RNA AFTER IN-SITU HYBRIDIZATION USING UNFIXED RAT-BRAIN TISSUE [J].
ASAN, E ;
KUGLER, P .
HISTOCHEMISTRY AND CELL BIOLOGY, 1995, 103 (06) :463-471
[6]   Ultrastructural features of tyrosine-hydroxylase-immunoreactive afferents and their targets in the rat amygdala [J].
Asan, E .
CELL AND TISSUE RESEARCH, 1997, 288 (03) :449-469
[7]   Interrelationships between tyrosine hydroxylase-immunoreactive dopaminergic afferents and somatostatinergic neurons in the rat central amygdaloid nucleus [J].
Asan, E .
HISTOCHEMISTRY AND CELL BIOLOGY, 1997, 107 (01) :65-79
[8]   Reduction of stress-induced behavior by antagonism of corticotropin-releasing hormone 2 (CRH2) receptors in lateral septum or CRH1 receptors in amygdala [J].
Bakshi, VP ;
Smith-Roe, S ;
Newman, SM ;
Grigoriadis, DE ;
Kalin, NH .
JOURNAL OF NEUROSCIENCE, 2002, 22 (07) :2926-2935
[9]   Corticotropin-releasing factor antagonist attenuates the "anxiogenic-like" effect in the defensive burying paradigm but not in the elevated plus-maze following chronic cocaine in rats [J].
Basso, AM ;
Spina, M ;
Rivier, J ;
Vale, W ;
Koob, GF .
PSYCHOPHARMACOLOGY, 1999, 145 (01) :21-30
[10]   IMPORTANCE OF FIXATION IN IMMUNOHISTOCHEMISTRY - USE OF FORMALDEHYDE SOLUTIONS AT VARIABLE PH FOR THE LOCALIZATION OF TYROSINE-HYDROXYLASE [J].
BEROD, A ;
HARTMAN, BK ;
PUJOL, JF .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1981, 29 (07) :844-850