Hallbeck M, Hermanson O, Blomqvist A
Division of Cell Biology, Department of Biomedicine and Surgery, Faculty of Health Sciences, University of Linköping, S-581 85 Linköping, Sweden.
J Comp Neurol. 1999 Aug 23;411(2):181-200.
Vasopressin released in the central nervous system has been shown to be involved both in homeostatic mechanisms (e.g., water balance, thermoregulation, cardiovascular regulation, metabolism, and antinociception) and in higher brain functions (e.g., social recognition and communication, and learning and memory). Many nuclear groups have been proposed to synthesize vasopressin, but available data are conflicting. We have used a sensitive in situ hybridization technique to identify the distribution of the neurons that may be the origin of the vasopressin in the central nervous system of the male Sprague-Dawley rat. Vasopressin mRNA-expressing neurons were most abundant in the hypothalamus (e.g., the paraventricular, supraoptic, and suprachiasmatic nuclei) but were also seen in the medial amygdaloid nucleus, the bed nucleus of stria terminalis, and the nucleus of the horizontal diagonal band. Previously unreported vasopressinergic neurons were seen in the entorhinal and piriform cortices, the ventral lateral portion of the parabrachial nucleus, the pedunculopontine nucleus, and the rostral part of the ventral periaqueductal gray matter and the adjacent portion of the mesencephalic reticular nucleus. Vasopressin mRNA expression suggestive of neuronal labeling was seen in the pyramidal layer of the CA1-3 fields and the dentate gyrus of the hippocampus. In addition, vasopressin mRNA expression, probably representing axonal mRNA, was detected over the hypothalamopituitary tract. No or insignificant preprovasopressin mRNA expression was present in the cerebellum, locus coeruleus, subcoeruleus, or the spinal cord. These findings provide novel information on the distribution of vasopressin neurons that are important for our understanding of how vasopressin acts in the brain.
已证明在中枢神经系统中释放的血管加压素既参与稳态机制(如水平衡、体温调节、心血管调节、新陈代谢和抗伤害感受),也参与高级脑功能(如社会识别与交流以及学习与记忆)。许多神经核团被认为可合成血管加压素,但现有数据相互矛盾。我们使用了一种灵敏的原位杂交技术来确定雄性斯普拉格 - 道利大鼠中枢神经系统中可能是血管加压素起源的神经元分布。表达血管加压素mRNA的神经元在下丘脑(如室旁核、视上核和视交叉上核)中最为丰富,但在杏仁内侧核、终纹床核和水平对角带核中也可见到。在内嗅皮质和梨状皮质、臂旁核腹外侧部分、脚桥核、导水管周围灰质腹侧部的头端部分以及中脑网状核的相邻部分发现了以前未报道的血管加压素能神经元。在海马体CA1 - 3区的锥体细胞层和齿状回中可见提示神经元标记的血管加压素mRNA表达。此外,在下丘脑垂体束上检测到可能代表轴突mRNA的血管加压素mRNA表达。在小脑、蓝斑、蓝斑下核或脊髓中未检测到或仅有微量的前血管加压素原mRNA表达。这些发现为血管加压素神经元的分布提供了新信息,这对于我们理解血管加压素在大脑中的作用方式很重要。