Finn A. Geneser

Distribution and morphology of serotonin-immunoreactive neurons in the brainstem of the New Zealand white rabbit

The aim of the present study was to demonstrate the morphology and distribution of the serotonergic neurons in the brainstem of the New Zealand white rabbit by using a highly specific immunocytochemical procedure. It was possible to divide the serotonergic neurons into a rostral group, which is situated in the mesencephalon and the rostral part of the pons containing four serotonergic nuclei, and a caudal group, which is located in the medulla and the caudal part of the pons containing five serotonergic nuclei. The localization of the serotonergic neurons is presented in a detailed brainstem atlas, and the distribution of the serotonergic neurons is in accordance with results obtained by other authors in different species.

Postnatal development of zinc-containing cells and neuropil in the hippocampal region of the mouse

The present study describes the postnatal development of zinc‐containing boutons and their neurons of origin in the hippocampal region of the mouse. Ages investigated for the development of zinc‐containing neuropil were postnatal days 0 (P0), P3, P7, P11, P15, P21, and P28. For zinc‐containing cell bodies P7, P15, P21, and P28 were studied.

New strategies for the treatment of Parkinson's disease hold considerable promise for the future management of neurodegenerative disorders

Neurodegenerative diseases are often consideredincurable with no efficient therapies to modifyor halt the progress of disease, and ultimatelylead to reduced quality of life and to death.Our knowledge of the nervous system in healthand disease has, however, increasedconsiderably during the last fifty years andtoday, neuroscience reveals promising newstrategies to deal with disorders of thenervous system.Some of these results have been implementedwith success in the treatment of Parkinsonsdisease, a common neurodegenerative illnessaffecting approximately 1% of the populationaged seventy or more. Parkinsons disease ischaracterized by a massive loss of dopaminergicneurons in the substantia nigra, leading tosevere functional disturbance of the neuronalcircuitry in the basal ganglia. A thoroughdescription of basal ganglia circuitry inhealth and disease is presented. We describehow the functional disturbances seen inParkinsons disease may be corrected atspecific sites in this circuitry by medicaltreatment or, in advanced stages of Parkinsonsdisease, by neurosurgical methods. The latterinclude lesional surgery, neuraltransplantation and deep brain stimulation,together with future treatment strategies usingdirect or indirect implantation of geneticallymodified cell-lines capable of secretingneurotrophic factors or neurotransmitters.Advantages and disadvantages are brieflymentioned for each strategy and theimplications for the future and the possibleuse of these interventions in otherneurodegenerative diseases are discussed, withspecial emphasis on deep brain stimulation.

Oriented sectioning of irregular tissue blocks in relation to computerized scanning modalities:: Results from the domestic pig brain☆

We present a new method allowing direct comparison between images obtained by present digital scanning modalities and histological sections from the same object. More specifically the paper illustrates how to orientate, embed, and section large irregular tissue blocks after magnetic resonance imaging (MRI) in such a way that accurate correlation of the digital data sets to histological sections is possible. The functionality and capability of the described procedure and slicing machine is illustrated by results from the pig brain. Accordingly, three pigs were MR-scanned, followed by perfusion fixation. The brains were removed, oriented according to the MR scans, embedded in alginate, and cut on a newly developed slicing machine. The tissue blocks were then stained to reveal grey and white matter and photographed before final sectioning on a cryostat into 80 microm thick sections which were Nissl-stained with toluidine. The results demonstrate how our method enables direct comparison between the pig brain MR images and the later obtained histological sections. The alginate embedding method and slicing machine offer the same possibilities for other parenchymateous organs and soft tissues and may, in addition, be of use in stereological analysis.

Distribution of neurons of origin of zinc-containing projections in the amygdala of the rat

The present study describes the distribution of neurons of origin of zinc-containing pathways in the amygdaloid complex of the rat, using the selenium method for simultaneous retrograde labeling of all zinc-containing neurons. With this method, vesicular ionic zinc is precipitated intravitally with selenium compounds and transported retrogradely to the parent neurons, where it can be visualized by silver amplification. Neurons labeled retrogradely with silver-amplified precipitate were observed in all amygdaloid nuclei except for the lateral olfactory tract nucleus, the accessory olfactory tract nucleus and the central nucleus. Very few labeled cell bodies were seen in the anterior amygdaloid area and the medial nucleus. The amygdalo-hippocampal area and the amygdalo-piriform transition area both showed a substantial number of labeled somata throughout their rostrocaudal extent. In the anterior cortical nucleus, very few labeled cell bodies were found in the rostral pole, whereas they were abundant in the caudal quarter of the nucleus. In the posterolateral cortical nucleus, the number of labeled cell bodies increased gradually; there were none in the rostral pole, but most of the neurons in the caudal part were labeled. The posteromedial cortical nucleus contained a great number of labeled somata, but with some variation in the rostrocaudal extent of the nucleus. Considerable numbers of labeled neurons were observed throughout the lateral nucleus. In the basolateral nucleus, a small number of labeled cell bodies was present in the rostral half, but a gradual increase was observed in the caudal direction. Finally, in the basomedial nucleus, very few labeled cell bodies were present in the rostral two-thirds, whilst a considerable number was encountered in the caudal one-third. Possible functional implications of neuronal zinc are considered. The distribution of neurons of origin of zinc-containing projections has been compared with previously described intrinsic connections of the rat amygdala, and tracts that may possibly be zinc-containing are outlined and discussed. It is concluded that in all probability a substantial proportion of the intrinsic connectivity of the rat amygdaloid complex is zinc-containing.

Histochemical distribution of zinc in the brain of the zebra finch (Taenopygia guttata)

The distribution of zinc was studied in the brain of the zebra finch (Taenopygia guttata) by means of the selenium histochemical method. A specifie pattern was seen, which usually correlated with the main known architectonic subdivisions. In addition, a few as yet unidentified structures were observed. In the telencephalon, the pallial components were stained with moderate to strong intensity. The only exceptions were the hyperstriatum intercalatus superior, a small medial area in the hyperstriatum accessorium and in the dorsolateral cortex, and the dorsomedial part of the hippocampal complex, which were virtually devoid of staining. Staining of the dorsal ventricular ridge components varied considerably. The archistriatum, the nucleus accumbens, the nucleus of the stria terminalis, the hyperstriatum ventrale and the lateral septum showed moderate to strong staining. The medial septum was weakly stained. The neostriatum showed a rather complex pattern of staining with unstained areas, such as the magnocellular nucleus of the anterior neostriatum, and other parts intensely stained, especially in its caudal region. Both paleostriatii primitivum and augmentatum showed a rostro-caudal gradient that was increasingly stained. We also observed an intensely stained area ventral to the fasciculus prosencephali lateralis and lateral to the tractus septomesencephalicus, a weakly to moderately stained band ventral to the lobus parolfactorius, an intensely stained zone along the lateral ventricle in the hyperstriatum ventrale, and an unstained almond-shaped nucleus in the lateral hyperstriatum ventrale. In the diencephalon, the hypothalamus showed a moderate to strong, rather uniform staining, whereas the thalamus was usually weakly to moderately stained, with the exception of a few unstained nuclei. Only the lateral nucleus of the habenula was stained, and with strong intensity. Most of the mesencephalon stained rather uniformly with a moderate to strong intensity. The most intense staining was seen in the substantia grisea centralis, the substantia grisea et fibrosa periventricularis, the torus semicircularis and the nucleus intercollicularis. The tectum opticum was virtually devoid of stain except for two light bands in the stratum griseum et fibrosum superficiale. The formatio reticularis was moderately stained. All the other structures were either weakly stained or unstained. Some staining was seen in the Purkinje and the granular layers of tha cerebellum, as well as around its internal nuclei. The pons and the medulla oblongata showed an overall moderate to intense staining, with the exception of a few unstained nuclei. When compared in three bird species belonging to different genera, zinc distribution shows remarkable similarities, despite species, age and methodological differences. The pattern of zinc staining suggests that this element may play an important role in integrative and autonomic functions.

Difference in monoamine oxidase B activity between C57 black and albino NMRI mouse strains may explain differential effects of the neurotoxin MPTP

Monoamine oxidase B (MAO-B) is the key enzyme in the conversion of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine(MPTP) to N-methyl-4-phenyl-pyridinium ion (MPP+) which causes degeneration of dopaminergic nigral neurons. Using a histochemical tetrazolium method for MAO-B with tyramine as substrate and chlorgyline for the inhibition of MAO-A, black C57 mice were found to have a higher brain MAO-B activity than similar aged albino NMRI mice. The difference, which was in general density rather than distribution, included the basal ganglia and the substantia nigra. The higher activity in C57 mice may explain differences in the susceptibility to MPTP.

Distribution of acetylcholinesterase and zinc in the visual cortex of the mouse

SummaryThe distributions of acetylcholinesterase (AChE) and zinc-containing boutons and their cells of origin in the visual cortex of the house mouse (Mus museulus domestieus) are described. The primary visual area is defined by both acetylcholinesterase and zinc staining. The AChE staining pattern is dark in upper layer I and layers IV and VI. It is light in layers II/III and V. The lack of a densely stained layer IV in the secondary visual cortices defines the borders between primary and secondary areas. Large, multipolar AChE-positive neurons are located throughout the cortical layers, but preferentially in layer VI. Dense zinc-positive neuropil in the primary visual cortex is apparent in layer lb, upper layer II/III, and layers V and VI. Neurons that give rise to zinc-containing boutons are situated in layers II/111 and VI. The medial and lateral borders can be distinguished by a bold contrast of staining in lower layer II/III; the secondary areas have more zinc-positive neurons, and the neuropil stains darker. A surprising observation of this study is the disparity between the mouse and rat visual cortex of the AChE staining pattern. Layer V is very light in the mouse, whereas a dark stain has been described in layer V of the rat. Layer VI stains heavily in the mouse while less AChE activity has been observed in layer VI of the rat.

Distribution and morphology of serotonin-immunoreactive axons in the retrohippocampal areas of the New Zealand white rabbit

This study provides a detailed light microscopic description of the morphology and distribution of serotonin-immunoreactive axons in the paleocortical retrohippocampal areas, viz. the subiculum, presubiculum, parasubiculum and entorhinal area, and the adjoining neocortical perirhinal and retrosplenial cortices of the New Zealand white rabbit. Serotonergic axons could be segregated into three different fiber types named fine fibers, beaded fibers and stem-axons. Fine fibers were evenly distributed thin axons with small fusiform/granular varicosities. Beaded fibers were thin axons with large varicosities, predominantly located in the retrohippocampal supragranular layers, where they often formed pericellular arrays. Stem-axons were thick straight, nonvaricose axons seen in the white matter of psalterium dorsale, alveus and the plexiform layer. The paleocortical retrohippocampal areas had a dense supragranular innervation with numerous tortuous fine and beaded fibers, intermingled in conglomerates with conspicuous varicosities forming pericellular arrays. In contrast, the neocortical area 17 and the lateral part of the perirhinal cortex (area 36) were innervated by evenly distributed fine fibers with a moderate number of small varicosities and few ramifications, whereas, the retrosplenial cortex (areas 29e, 29ab and 29cd), and the medial part of the perirhinal cortex (area 35) displayed an intermediate innervation pattern, probably reflecting the transitional nature of these areas being located between the paleo- and the neocortex. The described dualistic innervation pattern may functionally enable the serotonergic system to exert a strong influence on the supragranular layers of the retrohippocampal areas and thus on the neural input entering these areas from the perirhinal and neighboring polymodal association neocortices, whereas the innervation pattern in the adjoining neocortical areas points towards a more diffuse and general modulation of neural activity herein.

Convergence of Thalamic and Cholinergic Projections in the ‘Dentate Area’ of Lizards

The small-celled part of the medial cortex (Cxms) in lizards is comparable to the hippocampal area dentata in mammals. As in mammals, most of the afferents to this cortical area are arranged in sharply delimited laminae. In reptiles this lamination pattern is species-specific. In the lizard Tupinambis nigropunctatus projections from the multisensory dorsolateral thalamic nucleus (Dla) terminate in the middle one-third of the outer plexiform layer throughout the whole rostrocaudal extent of Cxms. In Podarcis hispanica the thalamic projections terminate not only in the middle one-third of Cxms but also in the inner plexiform layer. To find out whether the species-related variation of thalamic projections to Cxms is a solitary phenomenon or is related to variations of other afferents of Cxms, we studied the relationships between the thalamic and cholinergic projections from the basal telencephalon in the medial cortex of three lizard families: the Lacertidae, the Teiidae and the Gekkonidae. In the gekkonid lizards Gekko gecko and Eublepharius macularius, Dla projections were studied with the anterograde tracer Phaseolus vulgaris-leucoagglutinin. Projections were found in only the rostral one-third of Cxms where the fibers terminate in the superficial half of the outer plexiform layer and in the deep half of the inner plexiform layer. From acetylcholinesterase staining in the Cxms of representatives of these three lizard families, it appeared that the main cholinergic afferents terminate in the same subregions and the same laminae as the Dla projections. Therefore, there seems to be a close association between thalamic and cholinergic afferents in the Cxms of lizards, irrespective of their precise location in the cortex of the various species. This suggests a functional relationship between these two afferents of the dentate area in lizards.