TL;DR: It is demonstrated that OT acts in the medial amygdala during the initial exposure to facilitate social recognition in the mouse, and OT given before, but not after, the initial encounter restores social Recognition in OT knock-out mice.
Abstract: Oxytocin (OT) knock-out mice fail to recognize familiar conspecifics after repeated social exposures, despite normal olfactory and spatial learning abilities. OT treatment fully restores social recognition. Here we demonstrate that OT acts in the medial amygdala during the initial exposure to facilitate social recognition. OT given before, but not after, the initial encounter restores social recognition in OT knock-out mice. Using c-Fos immunoreactivity (Fos-IR) as a marker of neuronal activation in this initial encounter, we found similar neuronal activation in the wild-type (WT) and OT knock-out mouse in olfactory bulbs, piriform cortex, cortical amygdala, and the lateral septum. Wild-type, but not OT knock-out mice exhibited an induction of Fos-IR in the medial amygdala. Projections sites of the medial amygdala also failed to show a Fos-IR induction in the OT knock-out mice. OT knock-out, but not WT, mice showed dramatic increases in Fos-IR in the somatosensory cortex and the hippocampus, suggesting alternative processing of social cues in these animals. With site-specific injections of OT and an OT antagonist, we demonstrate that OT receptor activation in the medial amygdala is both necessary and sufficient for social recognition in the mouse.
TL;DR: The fates of adult OLPs are followed in Pdgfra-creERT2/Rosa26-YFP double-transgenic mice and it is found that they generated many myelinating oligodendrocytes during adulthood, but there is no evidence for astrocyte production in gray or white matter.
Abstract: About 4% of the cells in the adult rodent brain are PDGFRA+ NG2+ glia, derived from the oligodendrocyte lineage. Rivers and colleagues constructed a transgenic mouse to fate map the PDGFRA+ glia. In the adult corpus callosum, these cells generated substantial numbers of late-myelinating oligodendrocytes. In the cortex, little late myelination was observed; instead, PDGFRA+ precursors seemed to continuously generate small numbers of projection neurons mainly in piriform cortex.
TL;DR: The results confirm and extend previous observations that 5-HT2C receptor mRNA is present in many brain areas in addition to those autoradiographically shown to have the corresponding binding sites and that 4-HT1C receptor subtype is a principal 5- HT receptor in the brain.
TL;DR: A system of extensive corticocortical projections was revealed and it was indicated that different areas of the MD‐projection cortex have distinctive patterns in both their corticOCortical and subcortical projection.
Abstract: The efferent connections of the cortex projected upon by the mediodorsal thalamic nucleus (MD-projection cortex) have been re-examined autoradiographically in the rat following the microelectrophoretic injection of 3H-proline-leucine into different parts of the medial and sulcal MD-projection cortex. Contrary to previous negative findings, the present experiments revealed a system of extensive corticocortical projections and indicated that different areas of the MD-projection cortex have distinctive patterns in both their corticocortical and subcortical projections. Thus, cell of Brodmann's area 32 send axons to the retrosplenial cortex, area 29d, the peri- and entorhinal cortices, and the presubiculum. Both supragenual and more posterior regions of area 24 project to the retrosplenial cortex and area 29d, but only the posterior portion projects additionally to the entorhinal area and presubiculum. The cortical targets of axons from the sulcal MD-projection cortex are mainly the anterior part of the piriform cortex and, for the posterolateral part of the sulcal cortex (insular area), the retrosplenial area, lateral entorhinal area, and presubiculum. While the medial and sulcal divisions of the MD-projection cortex project upon one another, the medial-to-sulcal projection is in general denser than its reciprocal.
Earlier findings of projections to subcortical structures affiliated with the limbic system such as midline thalamic nuclei, hypothalamus, and paramedian mesencephalic tegmentum are confirmed, and appear to originate primarily in area 32 and the insular part of the sulcal cortex. The corticothalamic projection to MD in general terms reciprocates the organization seen in the thalamocortical projection from the various subnuclei within MD. Previously undocumented projections are demonstrated mainly from area 32 of the medial cortex and the insular part of the sulcal cortex to the lateral and basal amygdaloid nuclei, the medial part of the lateral septal nucleus, the nucleus accumbens, and the deep layers of the olfactory tubercle; the medial part of the lateral habenular nucleus receives a projection from areas 32 and 24. Projections to the pretectal area and superior colliculus appear to originate from all parts of the medial MD-projection cortex, but are markedly denser when the posterior part of area 24 is injected. The distribution of this corticotectal projection shows a highly characteristic configuration in which areas of high grain concentration surround areas of lower grain concentration.
TL;DR: It is suggested that DNPI functions in heterogeneous neuron populations as a neuron-specific Na(+)-dependent inorganic phosphate cotransport system predominantly expressed in the diencephalon of the rat.