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Dive into the research topics where William B. Forbes is active.

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Featured researches published by William B. Forbes.


Neuroscience & Biobehavioral Reviews | 1978

The effects of protein malnutrition on the developing central nervous system in the rat

Peter J. Morgane; Maravene Miller; T. Kemper; Warren C. Stern; William B. Forbes; R. Hall; J. Bronzino; J. Kissane; E. Hawrylewicz; Oscar Resnick

Abstract We have carried out a multi-disciplinary study of the effects of prenatal protein malnutrition on the developing rat brain. These experiments, involving anatomical, physiological, biochemical, and behavioral approaches, have revealed that malnutrition induced prenatally can affect various parameters of brain growth and development. Some of these effects can be reversed depending on when dietary restitutions are carried out. However, if protein malnutrition is maintained during the brain growth spurt or critical growth periods there are many permanent sequelae that cannot be reversed by subsequent restitution of high protein diets. We have reviewed the concept of critical periods of brain growth relative to the various aspects of neural morphogenesis in the rat, that is, the birth of neurons, migration of neurons, differentiation of neurons, and synapse formation. We have also discussed the rapid phases of brain growth in the rat as compared to similar phases in other species as a basis for determining whether the rat model can provide time-tables for brain growth in other species, including man. Different components of the brain, both morphological and chemical, have their own cycles of rapid development so that insults to the brain at particular periods affect particular aspects of brain chemistry and neuronal systems. Development of chemical circuits in the brain, such as the aminergic neurons, and their eventual adequate functioning, depends on development of the neurotransmitters themselves. These latter are markedly affected by protein malnutrition. Major physiological-behavioral states, such as the sleep-waking continuum, are markedly affected by protein malnutrition as are many behaviors. Some of these latter are merely late or retarded in development but others remain permanently altered. By approaching the problem of protein malnutrition from multiple points of view we have been able to pinpoint several brain areas showing the most drastic residua of early protein malnutrition and are beginning, by use of morphometric, electro-ontogenetic, biochemical development and behavioral studies, to define brain locales and basic mechanisms by which these insults produce their effects.


Brain Research Bulletin | 1977

Dorsal raphe, substantia nigra and locus coeruleus: Interconnections with each other and the neostriatum ☆

Daniel A. Pasquier; T. Kemper; William B. Forbes; Peter J. Morgane

Using a retrograde axonal transport method, direct projections to the neostriatum were demonstrated from the dorsal raphe nucleus, a large area of the ventral midbrain tegmentum (including the ventral tegmental area of Tsai, the substantia nigra pars compacta, reticulata and suboculomotoria), and the tegmentum ventral to the caudal red nucleus. A direct projection was also found from the mediodorsal part of the substantia nigra to the rostral part of the dorsal raphe nucleus. Projections from the entopeduncular nucleus (pallidum) and the lateral hypothalamic area to the lateral habenular nucleus, and from the latter to the dorsal raphe nucleus were also found. This habenular projection arises primarily from large neurons in the medial part of the lateral habenula and also from another group of small cells immediately adjacent to the medial habenular nucleus. A non-reciprocal connection of the dorsal raphe nucleus to the locus coernuleus was also found. On the basis of these results and the data available in the literature on the possible neurotransmitters used by these various structures, it is suggested that the dorsal raphe nucleus may play an important role in brain stem modulation of neostriatal function.


Experimental Neurology | 1975

Ontogeny of the levels of biogenic amines in various parts of the brain and in peripheral tissues in normal and protein malnourished rats.

Warren C. Stern; Maravene Miller; William B. Forbes; Peter J. Morgane; Oscar Resnick

Abstract The ontogenetic development of serotonin, 5-hydroxyindoleacetic acid, and norepinephrine in brain regions and in peripheral tissues was examined in normal and protein malnourished rats from birth to age 300 days. The malnourished rats, which received a diet low in protein starting 5 weeks prior to conception, showed significantly elevated brain and peripheral tissue levels of the biogenic amines and 5-hydroxyindoleacetic acid at birth. This is one of the earliest ages at which protein malnutrition has been reported to affect a major biochemical measure in the brain. In malnourished rats, brain concentrations of serotonin and 5-hydroxydoleacetic acid remained elevated at older ages, up to 300 days, with the largest effects (up to 200% increase) occurring in subtelencephalic brain regions. These changes in brain indole levels probably represent a general metabolic alteration of indoleamine metabolism since elevated indole concentrations were also observed in the heart, lung, and stomach. At most ages the increase in brain norepinephrine levels in malnourished rats was less pronounced than for the indoles. Also, no increase in norepinephrine concentration in the peripheral tissues were observed. With respect to norepinephrine concentrations, the brain appears to be more sensitive to the insult of protein malnutrition than do peripheral tissues. The present results demonstrate that rearing rats on a diet low in protein, but adequate in all other respects, significantly elevates the brain amine content at most ages from birth through 300 days of age.


Brain Research | 1974

Seizure susceptibility and brain amine levels following protein malnutrition during development in the rat

Warren C. Stern; William B. Forbes; Oscar Resnick; Peter J. Morgane

Abstract This report examines the change in seizure susceptibility in adult rats which were reared on a diet containing either normal or inadequate levels of protein. A significantly greater percentage of the protein malnourished rats convulsed at low to moderate intensities of electroconvulsive shock (ECS) than normals. Also, seizure duration in the malnourished subjects teneed to be longer than in the normals. Switching adult rats to the opposite diet, i.e. rats reared on normal diets now receive low protein diet and vice versa, had a moderating effect on seizure susceptibility, but full reversal of the effects of protein malnutrition was not achieved. In sum, protein malnutrition during development led to enhanced seizure susceptibility in adulthood, an effect which was only partially ameliorated by restoration of adequate dietary protein levels in adulthood. Prior studies have shown a strong inverse relationship between brain biogenic amine levels and seizure activity. In a second study we therefore investigated whether decreased regional brain levels of norepinephrine and serotonin were produced by chronic protein malnutrition. Suprrisingly, levels of these two amines were elevated in the brains of the protein malnourished rats and, therefore, changes in the levels of these neurochemicals cannot simply account for the increased seizure activity seen in rats reared on inadequate amounts of protein.


Neuroscience & Biobehavioral Reviews | 1979

Developmental protein malnutrition: Influences on the central nervous system of the rat ☆

Oscar Resnick; Maravene Miller; William B. Forbes; R. Hall; T. Kemper; Joseph D. Bronzino; Peter J. Morgane

Our group has been carrying out interdisciplinary studies on the effects of prenatal and postnatal protein malnutrition on the developing rat brain. Anatomical, physiological, biochemical and behavioral approaches using the same animal model have revealed that protein malnutrition affects the brain at various levels, i.e., (1) anatomical, as revealed by Golgi findings of deranged dendritic trees on analysis of cortical and subcortical areas; (2) physiological, as revealed by delayed sleep pattern maturation, disturbances in seizure thresholds, slowing of sensory cortico-cortical and thalamocortical evoked potentials, and changed power in hippocampal theta activity; (3) biochemical, as revealed by marked increases in biogenic amines dating from birth, as well as modifications in tryptophan metabolism; and (4) behavioral, as revealed by various changes in responses to different kinds of aversive stimulation. Reversal studies have revealed that many changes are permanent and not amenable to nutritional rehabilitation even at birth, which is before the brain growth spurt in the rat. Our paradigm closely mimicks the human condition of low level, chronic protein undernutrition and thus reveals the underlying disturbances due to malnutrition. The dietary reversal studies are attempts at pin-pointing critical brain growth periods, beyond which recovery of functions is not possible.


Brain Research Bulletin | 1994

The spatial organization of the peripheral olfactory system of the hamster. part I: Receptor neuron projections to the main olfactory bulb

Thomas A. Schoenfeld; Andrew N. Clancy; William B. Forbes; Foteos Macrides

The spatial organization of projections from olfactory receptor neurons to the main olfactory bulb (MOB) was studied in hamsters by using fluorescent stilbene isothiocyanates as retrograde tracers. Injections confined to small sectors of the MOB produce labeling of receptor neurons that is more restricted circumferentially (i.e., with respect to the medial-lateral and dorsal-ventral axes) than longitudinally (i.e., with respect to the rostral-caudal axis) along the mucosal sheet. This restricted labeling is also discontinuous, giving an initial impression that the peripheral input is only crudely organized with respect to the medial-lateral and dorsal-ventral axes of the nasal cavity. However, from analyses of serial sections, it is apparent that each set of mucosal segments shares convergent projections to a circumferential quadrant of the MOB with other segments that are positioned around a common domain of the nasal cavity airspace. The primary afferent projections to the MOB, thus, are organized rhinotopically (i.e., with respect to the three-dimensional position of receptor neurons in olfactory space) rather than mucosotopically.


Brain Research Bulletin | 1976

Horseradish peroxidase tracing of the lateral habenular-midbrain raphe nuclei connections in the rat

Daniel A. Pasquier; Clint Anderson; William B. Forbes; Peter J. Morgane

Connections of the habenular complex to the nuclei of the midline in the midbrain (interpeduncularis, medianus raphe, and dorsalis raphe) have been studied classically by anterograde degeneration in the monkey, the cat, and marsupials. Passing fibers from the medial septal nucleus and lateral preoptic area, however, have also been demonstrated which can complicate interpretation of these results. In this paper the habenular projections were studied in the rat by the retrograde axonal transport of horseradish peroxidase (HRP). After HRP injections in the medianus raphe nucleus labelled neurons appeared in the lateral habenular nucleus and parafascicular nucleus. Labelled neurons were also found in the lateral habenular nucleus after injections in either the dorsalis raphe nucleus or the caudal central gray substance. The habenular projections were always bilateral. There were no labelled neurons in the medial habenular nucleus after HRP injections in the medianus raphe especially on the dorsalis raphe neurons which have usually been thought of as functionally related to other brainstem structures. The present results suggest also that in the rat the lateral habenular nucleus might be the link between basal forbrain inputs and the limbic midbrain area. Thus, the raphe nuclei of the midbrain appear to be crucial regions for integrating two descending circuits: first, a limbic (through septum) circuit, and, second, a basal forebrain (through lateral habenular-preoptic area) circuit.


Brain Research Bulletin | 1977

Locus coeruleus-to-dorsal raphe input examined by electrophysiological and morphological methods☆

C.D. Anderson; Daniel A. Pasquier; William B. Forbes; Peter J. Morgane

In order to examine the hypothesis that the locus coeruleus (LC) projects directly to the nucleus raphe dorsalis (DR), electrical stimulation was applied to the LC of rats while recording from single neurons in the region of the DR. Slow firing units of the DR were not influenced by the stimulation, although faster firing units in the nearby substantia grisea centralis (SGC) were. These latter cells become oscillatory in their firing rates during LC stimulation. In parallel studies a retrograde transport technique was imployed to obtain morphological evidence regarding projections to DR. Placements of horseradish peroxidase precisely in the DR resulted in very sparse labeling in the LC, although positive transport occurred to other areas. The results indicate that the LC does not project directly to slow firing DR neurons, but does influence faster firing celles in the region of the SGC, probably by complex routes. Suggestions are made for the integration of these findings with earlier fluorescence studies.


Brain Research Bulletin | 1994

The spatial organization of the peripheral olfactory system of the hamster. Part II: Receptor surfaces and odorant passageways within the nasal cavity

Andrew N. Clancy; Thomas A. Schoenfeld; William B. Forbes; Foteos Macrides

The spatial organization of olfactory receptor surfaces and odorant passageways within the nasal cavity was studied in hamsters through descriptive and morphometric analyses of a complete stereotaxically defined series of coronal, sagittal, and horizontal sections through the snout. These analyses reveal that the caudal two-thirds of each cavity is divided into two longitudinally oriented medial and lateral channels. The olfactory mucosa that lines these two channels projects selectively onto the medial and lateral halves of the main olfactory bulb (MOB), respectively. Moreover, the ethmoturbinates of the caudal recesses create highly convoluted channels, lined by ventrally projecting mucosa, that lie ventral, lateral, and dorsal to a relatively smooth central channel lined by dorsally projecting mucosa. The rhinotopic map makes equivalent representations of medial and lateral olfactory space to the MOB but gives the smooth space lined by dorsally projecting mucosa a disproportionately larger representation on the MOB than the convoluted space lined by the more expansive ventrally projecting mucosa. Recent descriptions of the spatial distribution of probes for odorant receptor proteins conform closely to this organization, giving credence to the idea that rhinotopy is a basis for representing to the MOB the specific molecular features of odorant molecules.


Physiology & Behavior | 1974

Absence of ponto-geniculo-occipital (PGO) spikes in rats

Warren C. Stern; William B. Forbes; Peter J. Morgane

Abstract In contrast to the cat, EEG recordings from macroelectrodes in the lateral geniculate nucleus and occipital neocortex of rats (a) failed to show spiking activity during REM sleep, and (b) failed to show spiking activity after reserpine, i.p., during wakefulness or sleep. Other phasic activities during REM sleep, such as eye movements or muscle twitches, were present in rats. The absence of the ponto-geniculo-occipital spikes in rats, at least in the latter two regions, suggests that these monophasic events are not essential or fundamental characteristics of mammalian REM sleep.

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Oscar Resnick

Worcester Foundation for Biomedical Research

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Warren C. Stern

Worcester Foundation for Biomedical Research

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C. Tracy

Worcester Foundation for Biomedical Research

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Joseph D. Bronzino

Worcester Foundation for Biomedical Research

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Foteos Macrides

Worcester Foundation for Biomedical Research

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Maravene Miller

Worcester Foundation for Biomedical Research

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Daniel A. Pasquier

Worcester Foundation for Biomedical Research

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T. Kemper

Worcester Foundation for Biomedical Research

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Andrew N. Clancy

Worcester Foundation for Biomedical Research

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