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Forebrain Origins of Glutamatergic Innervation to the Rat Paraventricular Nucleus of the Hypothalamus: Differential Inputs to the Anterior Versus Posterior Subregions

Overview
Journal J Comp Neurol
Specialty Neurology
Date 2011 Apr 1
PMID 21452198
Citations 49
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Abstract

The hypothalamic paraventricular nucleus (PVN) regulates numerous homeostatic systems and functions largely under the influence of forebrain inputs. Glutamate is a major neurotransmitter in forebrain, and glutamate neurosignaling in the PVN is known to mediate many of its functions. Previous work showed that vesicular glutamate transporters (VGluTs; specific markers for glutamatergic neurons) are expressed in forebrain sites that project to the PVN; however, the extent of this presumed glutamatergic innervation to the PVN is not clear. In the present study retrograde FluoroGold (FG) labeling of PVN-projecting neurons was combined with in situ hybridization for VGluT1 and VGluT2 mRNAs to identify forebrain regions that provide glutamatergic innervation to the PVN and its immediate surround in rats, with special consideration for the sources to the anterior versus posterior PVN. VGluT1 mRNA colocalization with retrogradely labeled FG neurons was sparse. VGluT2 mRNA colocalization with FG neurons was most abundant in the ventromedial hypothalamus after anterior PVN FG injections, and in the lateral, posterior, dorsomedial, and ventromedial hypothalamic nuclei after posterior PVN injections. Anterograde tract tracing combined with VGluT2 immunolabeling showed that 1) ventromedial nucleus-derived glutamatergic inputs occur in both the anterior and posterior PVN; 2) posterior nucleus-derived glutamatergic inputs occur predominantly in the posterior PVN; and 3) medial preoptic nucleus-derived inputs to the PVN are not glutamatergic, thereby corroborating the innervation pattern seen with retrograde tracing. The results suggest that PVN subregions are influenced by varying amounts and sources of forebrain glutamatergic regulation, consistent with functional differentiation of glutamate projections.

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References
1.
Melis M, Succu S, Mascia M, Cortis L, Argiolas A . Extracellular excitatory amino acids increase in the paraventricular nucleus of male rats during sexual activity: main role of N-methyl-d-aspartic acid receptors in erectile function. Eur J Neurosci. 2004; 19(9):2569-75. DOI: 10.1111/j.0953-816X.2004.03362.x. View

2.
Ter Horst G, Luiten P . Phaseolus vulgaris leuco-agglutinin tracing of intrahypothalamic connections of the lateral, ventromedial, dorsomedial and paraventricular hypothalamic nuclei in the rat. Brain Res Bull. 1987; 18(2):191-203. DOI: 10.1016/0361-9230(87)90190-0. View

3.
Ribeiro-Barbosa E, Skorupa A, Cipolla-Neto J, Canteras N . Projections of the basal retrochiasmatic area: a neural site involved in the photic control of pineal metabolism. Brain Res. 1999; 839(1):35-40. DOI: 10.1016/s0006-8993(99)01685-6. View

4.
Eyigor O, Minbay Z, Cavusoglu I, Jennes L . Localization of kainate receptor subunit GluR5-immunoreactive cells in the rat hypothalamus. Brain Res Mol Brain Res. 2005; 136(1-2):38-44. DOI: 10.1016/j.molbrainres.2005.01.015. View

5.
Kenney M, Weiss M, Haywood J . The paraventricular nucleus: an important component of the central neurocircuitry regulating sympathetic nerve outflow. Acta Physiol Scand. 2002; 177(1):7-15. DOI: 10.1046/j.1365-201X.2003.01042.x. View