Distribution of 5-HT2A receptor immunoreactivity in the rat amygdaloid complex and colocalization with γ-aminobutyric acid

被引:28
作者
Bombardi, Cristiano [1 ]
机构
[1] Univ Bologna, Dept Vet Morphophysiol & Anim Prod, I-40064 Bologna, Italy
关键词
Amygdala; Double-immunohistochemistry; Immunoperoxidase; Interneurons; Pyramidal neurons; Serotonin; NUCLEUS RAPHE DORSALIS; CORTICAL AFFERENT CONNECTIONS; CALCIUM-BINDING PROTEINS; CENTRAL-NERVOUS-SYSTEM; SEROTONIN; 5-HT2A; PYRAMIDAL CELLS; IMMUNOHISTOCHEMICAL CHARACTERIZATION; LATERAL AMYGDALA; MIDBRAIN RAPHE; IMMUNOCYTOCHEMICAL LOCALIZATION;
D O I
10.1016/j.brainres.2010.11.055
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The 5-HT2A receptor (5-HT2Ar) is located in a variety of excitatory and inhibitory neurons in many regions of the central nervous system and is a major target for atypical antipsychotic drugs. In the present study, an immunoperoxidase experiment was used to investigate the distribution of 5-HT2Ar immunoreactivity in the rat amygdaloid complex. In the basolateral amygdala, the colocalization of 5-HT2Ar with inhibitory transmitter gamma-aminobutyric acid (GABA) was studied using double-immunofluorescence confocal microscopy. The staining pattern obtained was colchicine-sensitive. In fact, pretreatment with colchicine increased the number of 5-HT2Ar-immunoreactive somata. Accordingly, with the exception of the intercalated nuclei, the amygdaloid complex of colchicine-injected rats exhibited a high density of 5-HT2Ar-IR somata. Morphological analyses indicated that 5-HT2Ar was located on both excitatory and inhibitory neurons in the rat amygdaloid complex. In addition, double-immunofluorescence observations revealed that the great majority of GABA-immunoreactive neurons in the basolateral amygdala exhibited 5-HT2Ar immunoreactivity (66.3%-70.6% depending on the nucleus). These data help to clarify the complex role of the 5-HT2Ar in the amygdaloid complex suggesting that this receptor can regulate amygdaloid activity by acting on different neuronal populations. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 128
页数:17
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