Hyperpallium Apicale Research Articles

Female stimuli trigger gene expression in male pigeons

The immediate early gene zenk encodes transcriptional regulators and is believed to be one of the first steps in the formation of long-term memories associated with a given stimulus. In this study, we investigated the expression of ZENK protein product in brain regions that are likely involved in the processing of social stimuli, such as a potential mate. Male pigeons (Columba livia) were exposed to one of the following: (1) a live female pigeon, (2) a video playback of a female pigeon, (3) a video playback of a female cockatoo, or (4) an empty stimulus chamber. The brains were then processed immunohistochemically using an antibody against ZENK protein. When the stimulus was a live pigeon compared to all other stimuli, there were more numerous and more darkly-stained ZENK-positive cells in three “association” regions of the telencephalon: the hyperpallium apicale, the lateral portion of the intermediate nidopallium, and the medial nidopallium. There were no significant differences among the video-playback stimuli. The results suggest that the level of ZENK expression in these “association” regions was influenced not only by the visual presence of a potential mate, but by the presence of non-visual signals, the quality of the image, and the real-time interaction with the stimulus.

Connections of the ventrobasal forebrain in the domestic chick (Gallus domesticus)

Event Abstract Back to Event Connections of the ventrobasal forebrain in the domestic chick (Gallus domesticus) Eszter Bálint1* and Andras Csillag1 1 Department of Anatomy, Semmelweis University, Hungary The ventrobasal forebrain of the avian brain includes the olfactory tubercle (TO). Recent investigation has indicated greater behavioural significance of this region even in microsmatic avian species. The pathway tracer Fast Blue was injected in six two-week-old chicks and the retrogradely labelled cell bodies were detected and charted using confocal laser scanning fluorescent microscopy. Telencephalic sources of TO projections were found in several arcopallial divisions (representing parts of the avian amygdala), nucleus accumbens, medial striatum (MSt), ventral pallidum (VP), hippocampus, hyperpallium apicale, lateral septum, temporoparietal cortex and piriform cortex. Diencephalic projections arose from the nucleus dorsomedialis anterior (DMA) and nucleus dorsolateralis anterior (DLA) of thalamus and the lateral hypothalamus (LHy). In the mesencephalon, labelled cells were abundant in the ventral tegmental area (VTA), nucleus interpeduncularis and periaqueductal gray (PAG). In the rest of the brainstem, the most prominent accumulation of labelled cells was observed in the locus coeruleus (LoC). In certain cases, anterograde tracer (biotinylated dextrane amine) injections were deposited in the TO/ventral striatal border region. In the telencephalon, labelled fibers were abundant in the MSt, hyperpallium densocellulare, VP, mesopallium and in the nucleus taeniae amygdalopallii. In the diencephalon, high amount of labelled fibers were found in the LHy, paraventricular nucleus and DLA. In the midbrain, the bulk of fibers were found in the VTA, nucleus papillioformis, substantia nigra and PAG. In the rest of the brainstem, the most prominent accumulation of labelled fibers were found in the LoC, subcoeruleus nuclei and the raphe. Conference: 12th Meeting of the Hungarian Neuroscience Society, Budapest, Hungary, 22 Jan - 24 Jan, 2009. Presentation Type: Poster Presentation Topic: Developmental neurobiology and subcortical functions Citation: Bálint E and Csillag A (2009). Connections of the ventrobasal forebrain in the domestic chick (Gallus domesticus). Front. Syst. Neurosci. Conference Abstract: 12th Meeting of the Hungarian Neuroscience Society. doi: 10.3389/conf.neuro.01.2009.04.043 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 27 Feb 2009; Published Online: 27 Feb 2009. * Correspondence: Eszter Bálint, Department of Anatomy, Semmelweis University, Budapest, Hungary, pupalibera@yahoo.com Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Eszter Bálint Andras Csillag Google Eszter Bálint Andras Csillag Google Scholar Eszter Bálint Andras Csillag PubMed Eszter Bálint Andras Csillag Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

Greater hippocampal neuronal recruitment in food‐storing than in non‐food‐storing birds

Previous research has shown heightened recruitment of new neurons to the chickadee hippocampus in the fall. The present study was conducted to determine whether heightened fall recruitment is associated with the seasonal onset of food-storing by comparing neurogenesis in chickadees and a non-food-storing species, the house sparrow. Chickadees and house sparrows were captured in the wild in fall and spring and received multiple injections of the cell birth marker bromodeoxyuridine (BrdU). Birds were held in captivity and the level of hippocampal neuron recruitment was assessed after 6 weeks. Chickadees showed significantly more hippocampal neuronal recruitment than house sparrows. We found no seasonal differences in hippocampal neuronal recruitment in either species. In chickadees and in house sparrows, one-third of new cells labeled for BrdU also expressed the mature neuronal protein, NeuN. In a region adjacent to the hippocampus, the hyperpallium apicale, we observed no significant differences in neuronal recruitment between species or between seasons. Hippocampal volume and total neuron number both were greater in spring than in fall in chickadees, but no seasonal differences were observed in house sparrows. Enhanced neuronal recruitment in the hippocampus of food-storing chickadees suggests a degree of neurogenic specialization that may be associated with the spatial memory requirements of food-storing behavior.

Annual Cycle of the Black-Capped Chickadee: Seasonality of Food-Storing and the Hippocampus

Previous research presents a mixed picture of seasonal variation in the hippocampus of food-storing black-capped chickadees. One field study has shown an October peak in hippocampus volume, although laboratory studies conducted to determine whether photoperiod regulates this seasonal growth have failed to find changes in the size of the hippocampus. To resolve the discrepancy between field and lab reports we examined caching activity, hippocampal volume, and neurogenesis in adult male black-capped chickadees at four times over the annual cycle: October, January, April and July. We found that more birds stored food in October than at other times of year, but did not observe a significant change in the size of the hippocampus over the annual cycle. Telencephalon volume, however, was larger in October than in July. Hippocampal neuronal recruitment showed a significant peak in January, but there was no seasonal change in neuronal recruitment in the adjacent hyperpallium apicale. These results indicate that there might be seasonal variation in the recruitment of new neurons into the hippocampus of chickadees without overall seasonal change in hippocampal size.

Organization of telencephalotectal projections in pigeons: Impact for lateralized top-down control

Birds display hemispheric specific modes of visual processing with a dominance of the right eye/left hemisphere for detailed visual object analysis. In pigeons, this behavioral lateralization is accompanied by morphological left–right differences in the ascending tectofugal pathway. This system is also asymmetrically modulated by descending telencephalotectal input whereby the left forebrain displays a much more pronounced physiological control over ipsilateral left and contralateral right visual thalamic processes. In the present study we aimed to answer the question if this top-down asymmetry that up to now had been demonstrated in single cell recording studies is due to anatomical asymmetries in the size of the fiber systems descending from the telencephalon to the tectum.We approached this question by means of a quantitative retrograde tracing study. Cholera toxin subunit B (CtB) was injected unilaterally into either the left or right optic tectum of adult pigeons. After immunohistochemical detection of CtB-positive cells, the number of ipsi- and contralaterally projecting neurons was estimated. Retrogradely labeled cells were located within the arcopallium, the hyperpallium apicale (HA) and the temporo-parieto-occipital area (TPO). Descending projections from HA, arcopallium, and TPO were mainly or exclusively ipsilateral with the contralateral projection being extremely small. Moreover, there was no difference between left and right hemispheric projections. These anatomical data sharply contrast with behavioral and electrophysiological ones which reveal an asymmetric and bilateral top down control. Therefore, contralateral and lateralized forebrain influences onto tectofugal processing are possibly not the direct result of asymmetrical descending axon numbers. Those influences emerge by a lateralized intra- and/or interhemispheric integration of ascending and descending input onto the rotundus.

C-fos induction in forebrain areas of two different visual pathways during consolidation of sexual imprinting in the zebra finch ( Taeniopygia guttata)

Two forebrain areas in the hyperpallium apicale and in the lateral nidopallium of isolated male zebra finches are highly active (2-deoxyglucose technique) on exposure to females for the first time, that is first courtship. These areas also demonstrate enhanced neuronal plasticity when screened with c-fos immunocytochemistry. Both are areas involved in the processing of visual information conveyed by the two major visual pathways in birds, strengthening our hypothesis that courtship in the zebra finch is a visually guided behaviour. First courtship and chased birds show enhanced c-fos induction in the hyperpallial area, which could represent neuronal activity reflecting changes in the immediate environment. The enhanced expression of fos in first courtship birds in lateral nidopallial neurons indicates imminent long-lasting changes at the synaptic level that form the substrate for imprinting, a stable form of learning in birds.

Distribution and onset of retinaldehyde dehydrogenase (zRalDH) expression in zebra finch brain: Lack of sex difference in HVC and RA at early posthatch ages

Using in situ hybridization to detect the expression of the retinoic acid synthesizing enzyme (retinaldehyde dehydrogenase: zRalDH) mRNA, we mapped the distribution of its expression in adult zebra finch brain. In the neural song circuit, strong expression was found in high vocal center (HVC), para-HVC, and at a very low level in the robust nucleus of the arcopallium (RA). The expression in HVC and RA was found in both males and females. Outside of the song system, major areas of expression were in medial nidopallium (N), hyperpallium apicale (HA), mesopallium ventrale (MV), taenial amygdala (TnA), cerebellar Purkinje cells, and nucleus isthmo-opticus (IO). In nestlings, we found zRalDH mRNA expression in HVC and RA as early as posthatch day 4 or 5 (P4-5), although the expression varied among individuals. Thus, retinoic acid synthesis in HVC and RA could participate in song system formation and development. However, we found no sex difference in volume or intensity of zRalDH and androgen receptor (AR) expression in HVC and RA at P11 prior to the development of significant size dimorphisms in these nuclei. The size of HVC in females at P11 defined by zRalDH expression was greater than that in adult females, suggesting that HVC might experience net cell loss between P11 and adulthood.

An examination of avian hippocampal neurogenesis in relationship to photoperiod

More neurons are recruited into the hippocampus of adult black-capped chickadees in the fall than at other times of year. To determine whether declining photoperiod and photorefractoriness are cues stimulating this neuronal recruitment; we examined three groups of chickadees receiving bromodeoxyuridine injections 10 days before being killed: one group was photostimulated with long days (15L), a second group was held on 15L until photorefractory and another group was held on 15L until photorefractory, then moved to short days (8L). Measures of neurogenesis revealed no significant differences in hippocampal neuronal recruitment. However, neuronal recruitment was increased in the hyperpallium apicale of photostimulated birds. These results suggest that declining photoperiod per se is not a major factor regulating enhanced neuronal recruitment to the hippocampus in the fall.

Topological relation of chick thalamofugal visual projections with hyper pallium revealed by three color tracers

In birds, there are two visual projections from retina to higher pallium, i.e., tectofugal and thalamofugal pathways. The latter one is lateralized in chick and suggested to be involved in visually evoked social behavior, like recognition of novelty, predator, and conspecific animals. We wanted to establish functionally relevant topological connection map between thalamic nuclei and hyperpallium apicale (HA) and carried out tracing study with three color fluorescent tracers. The tracers were serially injected in HA either along with the medial–lateral (M–L) or anterior–posterior (A–P) axis. We found that M–L axis and A–P axis in HA were transferred into the dorsal–ventral axis and the medial–lateral axis, respectively within the nucleus geniculatus lateralis pars dorsalis (GLd). In another word, the medial part of nucleus dorsolateralis anterior thalami pars lateralis (DLLv) projected to anterior part of HA and the ventral part of nucleus dorsolateralis anterior thalami pars lateralis pas ventralis (DLLd) projects to lateral HA. This result suggests that thalamus would process information in parallel through each subnuclei and elaborate coordination among them in relation to topological map presented in higher pallium.

Telencephalic projections to the nucleus of the basal optic root and pretectal nucleus lentiformis mesencephali in pigeons

In birds, the nucleus of the basal optic root (nBOR) of the accessory optic system (AOS) and the pretectal nucleus lentiformis mesencephali (LM) are involved in the analysis of optic flow and the generation of the optokinetic response. In several species, it has been shown that the AOS and pretectum receive input from visual areas of the telencephalon. Previous studies in pigeons using anterograde tracers have shown that both nBOR and LM receive input from the visual Wulst, the putative homolog of mammalian primary visual cortex. In the present study, we used retrograde and anterograde tracing techniques to further characterize these projections in pigeons. After injections of the retrograde tracer cholera toxin subunit B (CTB) into either LM or nBOR, retrograde labeling in the telencephalon was restricted to the hyperpallium apicale (HA) of the Wulst. From the LM injections, retrograde labeling appeared as a discrete band of cells restricted to the lateral edge of HA. From the nBOR injections, the retrograde labeling was more distributed in HA, generally dorsal and dorso-medial to the LM-projecting neurons. In the anterograde experiments, biotinylated dextran amine (BDA) was injected into HA and individual axons were reconstructed to terminal fields in the LM and nBOR. Those fibers projecting to the nBOR also innervated the adjacent ventral tegmental area. However, tracing of BDA-labeled axons revealed no evidence that individual neurons project to both LM and nBOR. In summary, our results suggest that the nBOR and LM receive input from different areas of the Wulst. We discuss how these projections may transmit visual and/or somatosensory information to the nBOR and LM.