Androgen receptor expressing neurons that project to the paraventricular nucleus of the hypothalamus in the male rat

被引:44
|
作者
Williamson, Martin [1 ]
Viau, Victor [1 ]
机构
[1] Univ British Columbia, Life Sci Ctr, Dept Cellular & Physiol Sci, Vancouver, BC V6T 1Z3, Canada
关键词
androgen receptor; FluoroGold; paraventricular nucleus of the hypothalamus; hypothalamic-pituitary-adrenal axis; catecholamine neurons;
D O I
10.1002/cne.21411
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Androgen receptors are distributed throughout the central nervous system and are contained by a variety of nuclei that are known to project to or regulate the paraventricular nucleus (PVN) of the hypothalamus, the final common pathway by which the brain regulates the hypothalamic-pituitary-adrenal (HPA) response to homeostatic threat. Here we characterized androgen receptor staining within cells identified as projecting to the PVN in male rats bearing iontophoretic or crystalline injections of the retrograde tracer FluoroGold aimed at the caudal two-thirds of the nucleus, where corticotropin-releasing hormone-expressing neurons are amassed. Androgen receptor (AR) and FluoroGold (FG) double labeling was revealed throughout the limbic forebrain, including scattered numbers of cells within the anterior and posterior subdivisions of the bed nuclei of the stria terminalis; the medial zone of the hypothalamus, including large numbers of AR-FG-positive cells within the anteroventral periventricular and medial preoptic cell groups. Strong and consistent colabeling was also revealed throughout the hindbrain, predominantly within the periaqueductal gray and the lateral parabrachial nucleus, and within various medullary cell groups identified as catecholaminergic, predominantly C1 and A1 neurons of the ventral medulla. These connectional data predict that androgens can act on a large assortment of multimodal inputs to the PVN, including those involved with the processing of various types of sensory and limbic information, and provide an anatomical framework for understanding how gonadal status could contribute to individual differences in HPA function.
引用
收藏
页码:717 / 740
页数:24
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