Search PubMed⌕ Search

Biomedical subjects

A J McDonald

Publications and source records attributed to A J McDonald.

At least 19 recordsLinked to original sources
PubMed1995

Neuropeptide Y and somatostatin-like immunoreactivity in neurons of the monkey amygdala.

Neurons in the monkey amygdala exhibiting neuropeptide Y-like immunoreactivity and somatostatin-like immunoreactivity were identified using an avidin-biotin immunohistochemical technique. Differential co-existence of the two peptides was demonstrated using two-color immunoperoxidase and adjacent section methods. Numerous neuropeptide Y-positive neurons were observed in the basolateral and superficial amygdaloid nuclei. A moderate number of neuropeptide Y-positive neurons was seen in the medial subdivision of the central nucleus, but only a few neurons were observed in the lateral subdivision. Numerous somatostatin-positive neurons were stained in all major amygdaloid nuclei and always outnumbered neuropeptide Y-positive cells. All amygdaloid nuclei contained numerous peptide-positive fibers whose density varied depending on the nucleus. Approximately 90% of neuropeptide Y-positive neurons also exhibited somatostatin-like immunoreactivity. The percentage of somatostatin-positive neurons that exhibited neuropeptide-Y immunoreactivity varied in different nuclei. In the superficial amygdaloid nuclei, medial subdivision of the central nucleus and most portions of the basolateral nuclei the predominant cell type stained with both the neuropeptide Y and somatostatin antibodies was a spine-sparse non-pyramidal neuron. In the dorsal portion of the lateral nucleus, however, most peptide-positive neurons had spiny dendrites. Only the cell bodies and proximal dendrites of somatostatin-positive neurons in the lateral subdivision of the central nucleus were immunostained. This study demonstrates that specific cell populations in the primate amygdala contain neuropeptide Y, somatostatin or both peptides. Most peptide-positive neurons in the basolateral and superficial amygdaloid nuclei appear to be local circuit neurons that contribute to the dense plexus of peptide-positive axons in these regions. The finding of neurons with spiny dendrites in the dorsal part of the lateral nucleus suggests that these cells may be functionally different from peptide-positive neurons in other portions of the basolateral amygdala. The lateral subdivision of the central nucleus is distinguished from other amygdaloid nuclei by containing a large population of somatostatin-positive neurons that do not exhibit neuropeptide Y immunoreactivity.

Amygdala↗
PubMed1994

Neuronal localization of glutamate receptor subunits in the basolateral amygdala.

Antibodies to the NMDAR1 glutamate receptor subunit and the GluR1 and GluR2/3 subunits of the AMPA glutamate receptor were used to localize these receptor components in the basolateral amygdala (ABL) of the rat and monkey. A similar localization pattern was observed in both species. Pyramidal neurons exhibited high levels of NMDAR1 and GluR2/3 immunoreactivity (ir), but low levels of GluR1-ir. Some non-pyramidal cells exhibited high levels of NMDAR1-ir or GluR1-ir, but none exhibited significant levels of GluR2/3-ir. This differential localization of receptor subunits suggests that glutamate receptors will exhibit specific functional properties in distinct subpopulations of ABL neurons.

Amygdala↗
PubMed1994

Calretinin immunoreactive neurons in the basolateral amygdala of the rat and monkey.

The calcium-binding protein calretinin was localized in the basolateral amygdala (BLA) of the rat and monkey using immunohistochemical techniques. In both species the predominant cell type exhibiting calretinin-like immunoreactivity (CR-ir) was a small non-pyramidal neuron with a bipolar or bitufted dendritic arborization pattern. Some pyramidal neurons also exhibited light CR-ir. In the monkey there was an additional population of large moderately-stained neurons with well-stained dendrites. These results indicate that calretinin is found in specific cell types in BLA. The small non-pyramidal CR-ir neurons are morphologically similar to BLA neurons that exhibit immunoreactivity for vasoactive intestinal polypeptide (VIP). These CR-ir neurons in BLA closely resemble the small bipolar CR-ir neurons of the cerebral cortex.

Amygdala↗
PubMed1994

A sexually dimorphic population of CRF neurons in the medial preoptic area.

The neuropeptide corticotropin-releasing factor (CRF) is thought to mediate the induction of a constellation of behavioral, endocrine, and autonomic responses which are important for an animal's adaptation to stressful events. We have found that the anteroventral periventricular preoptic nucleus (AVPv) and medial preoptic nucleus (MPN) of colchicine-injected female rats contained numerous intensely stained CRF-immunoreactive neurons. The AVPv/MPN in males contained very few CRF-immunoreactive neurons per section, even in colchicine-injected animals. This sexually dimorphic population of CRF-immunoreactive neurons in the AVPv may play some role in the sex-related differences in hormonal responses to stress and/or in the control of female reproductive events.

Animals↗
PubMed1993

Corticoamygdaloid and corticocortical projections of the rat temporal cortex: a Phaseolus vulgaris leucoagglutinin study.

The projections of the rat temporal cortex to the amygdala and cerebral cortex were studied using the sensitive anterograde tracer, Phaseolus vulgaris leucoagglutinin. These studies revealed that the core of temporal area 1 had no projections to the amygdala but did send efferents to several cortical fields that projected to the amygdala, including temporal area 2, temporal area 3, the lateral occipital area 2, and a cortical zone along the dorsal, rostral and caudal borders of temporal area 1 ("Tel fringe"). The temporal area 1 fringe cortex had light projections to the amygdala that were confined to the dorsolateral subdivision of the lateral amygdaloid nucleus. Temporal area 2 and the caudal portion of temporal area 3 had projections to both the dorsolateral and ventromedial subdivisions of the lateral nucleus; the projection from temporal area 2 targeted mainly the ventromedial subdivision, whereas the projection from the caudal portion of temporal area 3 terminated primarily in the dorsolateral subdivision. The rostral portion of temporal area 3 had projections to both subdivisions of the lateral nucleus and to the basal magnocellular nucleus. Temporal areas 2 and 3 also had light projections to the lateral capsular subdivision of the central amygdaloid nucleus. Temporal cortical areas exhibited extensive reciprocal connections with each other. Temporal areas with amygdaloid projections also had extensive projections to the perirhinal cortex. The results of the present investigation, in conjunction with other studies of temporal cortical connections, suggest that all temporal regions projecting to the amygdala are multimodal sensory areas. The core of temporal area 1, which is probably the primary auditory area, apparently has no direct projections to the amygdala. The differential projections of different temporal areas to the amygdala suggests the existence of several distinct multimodal pathways arranged in a parallel configuration.

Amygdala↗
PubMed1993

Identification of putative nitric oxide producing neurons in the rat amygdala using NADPH-diaphorase histochemistry.

Putative nitric oxide-containing neurons in the rat amygdala were studied using reduced nicotinamide adenine dinucleotide phosphate diaphorase histochemistry. All nuclei of the amygdala contained subpopulations of diaphorase-positive neurons, but the staining intensity of different subpopulations varied. Intensely stained neurons exhibited labeling of the cell body and the entire dendritic arborization. The lateral nucleus had the greatest concentration of intensely labeled cells. Many intensely labeled neurons were located along nuclear boundaries and fiber bundles. In addition to neuronal staining, there was a differential staining of the neuropil in different amygdaloid nuclei. In the basolateral and cortical nuclei the diaphorase-positive cells were non-pyramidal neurons that resembled those containing somatostatin and neuropeptide Y. The distribution and neuronal morphology of labeled neurons in the central nucleus and anterior amygdaloid area suggests that diaphorase-positive cells in these areas may be cholinergic. Recent studies have shown that the enzyme responsible for neuronal diaphorase activity is actually the synthetic enzyme for the newly discovered neurotransmitter nitric oxide. Since there is evidence that nitric oxide plays an important role in excitotoxic neuronal degeneration, the neurons identified in the present study may be involved in degenerative diseases of the amygdala.

Amygdala↗
PubMed1993

Oral labetalol versus oral nifedipine in hypertensive urgencies in the ED.

Therapy in hypertensive urgencies is debated and complicated by the side effects of available agents. In a prospective, randomized, open labeled study, the use of oral labetalol, an alpha- and beta-adrenergic blocker, with oral nifedipine in hypertensive urgencies in the emergency department was compared. Patients with diastolic blood pressures (DBP) of more than 120 mm Hg without criteria for a hypertensive emergency were eligible. The drugs were given in a loading manner with doses and timing based on their respective pharmacokinetics until a DBP of 110 mm Hg or lower was obtained or 4 hours had passed. Either an initial labetalol dose of 200 mg and a repeat dose of 100 to 200 mg at 2 hours, depending on the DBP or nifedipine, 10-mg bite and swallow every hour up to a total dose of 20 mg were given. Ten patients were enrolled into each study group. A 100% response rate was defined as a DBP of 110 mm Hg or less was observed for nifedipine and an 80% response rate for labetalol (P > .2) was observed. The mean time to control was 67.5 minutes for labetalol and 60.0 minutes for nifedipine (P > .2). The pretreatment pressure for labetalol was 195/127 mm Hg and for nifedipine was 198/128 mm Hg (P > .2), which decreased to a posttreatment pressure for labetalol of 154/100 mm Hg and for nifedipine of 163/100 mm Hg (P > .2). The mean decrease in systolic (SBP)/DBP was 42.6/26.5 mm Hg with labetalol and 34.9/28.4 mm Hg for nifedipine (P > .2). No significant side effects occurred with either drug.(ABSTRACT TRUNCATED AT 250 WORDS)

Administration, Oral↗
PubMed1992

The inferior colliculus: calbindin and parvalbumin immunoreactivity in neural grafts.

The inferior colliculus was selected as a brain stem site for study of neural grafting and identification of calcium binding proteins. Unilateral ablation sites of eight midbrain inferior colliculus in adult Long-Evans rats were implanted with E17-18 caudal tectum. After 2 to 9 months animals were sacrificed and sections reacted using antibodies for calbindin and parvalbumin. The central nucleus of normal inferior colliculus shows high density of neuronal and fiber staining for parvalbumin. Typical graft cores had similar staining distributions including discoid and stellate neuron populations. Graft cores showed low densities of reactivity for calbindin comparable to central nucleus. In surrounding graft regions there was substantive-neuronal and fiber labeling for calbindin and parvalbumin including stellate neuron populations normally found in the dorsal and lateral nuclei of inferior colliculus. These results demonstrate that the expression of calcium binding proteins in tectal grafts resembles that of inferior colliculus.

Animals↗
PubMed1992

Projection neurons of the basolateral amygdala: a correlative Golgi and retrograde tract tracing study.

This study analyzed the projection neurons of the anterior subdivision of the rat basolateral amygdaloid nucleus (BLa) by correlating the morphology of Golgi-stained neurons with the morphology of neurons that were retrogradely labeled by injections into the main terminal fields of BLa. In each animal multiple injections of horseradish peroxidase (HRP) and wheat germ agglutinin-conjugated HRP were made into the prefrontal cortex and rostral striatum. These injections labeled approximately 85% of BLa neurons. The great majority of labeled neurons were the same shape and relative size as the pyramidal (class I) neurons described in previous Golgi studies. The unlabeled neurons appeared to correspond to the nonpyramidal (class II and class III) neurons described in Golgi studies. Thus this investigation provides experimental evidence that the pyramidal neurons are the main projection neurons of BL, whereas most of the nonpyramidal cells are local circuit neurons.

Amygdala↗
PubMed1992

Biocytin injections produce selective neuronal labeling in the rat CNS.

Large injections of biocytin into the lateral ventricle or brain resulted in the labeling of particular neuronal subpopulations in the rat CNS. Localization was accomplished using the avidin-biotin-peroxidase technique. In many cases the staining of neurons was totally complete and resembled that obtained with the Golgi technique. Regions containing labeled cells included the olfactory bulb, cerebral cortex, hippocampus, amygdala, striatum, hypothalamus, superior and inferior colliculi, cerebellar cortex, and dorsal horn of the spinal cord. Only particular cell types were labeled in each of these regions. The results of this study suggest that there is selective uptake and/or retention of biocytin, or a biotinylated metabolite of biocytin, by subpopulations of CNS neurons.

Animals↗
PubMed1992

Neuroanatomical labeling with biocytin: a review.

Recent studies have shown that biocytin may have multiple applications in neuroanatomical studies. Biocytin may be injected into the brain by iontophoresis or by pressure injection methods, and localized in tissue sections using avidin-conjugated labels. It is taken up by neurons and rapidly transported down axons in an anterograde fashion. Axons are completely labeled in a Golgi-like manner and can be examined at both light and electron microscopic levels. Biocytin can also be used in retrograde tract tracing experiments, although in some cases it appears that fibers must be damaged to produce such labeling. Retrogradely labeled cells may be completely labeled, resembling neurons stained with the Golgi technique. Individual neurons can also be labeled in a Golgi-like manner by uptake of biocytin from the extracellular space. Thus, it appears that biocytin is an especially versatile marker for neuroanatomical investigations.

Animals↗
PubMed1991

Organization of amygdaloid projections to the prefrontal cortex and associated striatum in the rat.

The organization of connections between the amygdala, prefrontal cortex and striatum was studied using anterograde and retrograde tract tracing techniques in the rat. The anterograde transport of Phaseolus vulgaris leucoagglutinin and wheat germ agglutinin conjugated to horseradish peroxidase was used to examine the striatal projections of the prefrontal cortex. These studies revealed that the prelimbic area of the medial prefrontal cortex projects mainly to the medial part of the striatum, whereas the dorsal agranular insular area of the lateral prefrontal cortex projects mainly to the ventrolateral part of the striatum. The organization of amygdaloid projections to the prefrontal cortex and its associated portions of the striatum was investigated using the fluorescence retrograde tract tracing technique. Different color fluorescent dyes, True Blue and Diamidino Yellow, were injected into the prefrontal cortex and striatum. These studies demonstrated that medial portions of the basolateral nucleus, and adjacent portions of the lateral, basomedial and amygdalo-hippocampal nuclei, project to both the medial prefrontal cortex and its associated medial striatal region. The rostral pole and lateral portions of the basolateral nucleus project to both the lateral prefrontal cortex and its associated lateral striatal region. Many neurons in the basolateral amygdaloid nucleus, and to a lesser extent other amygdaloid nuclei, were double-labeled in these experiments, indicating that these cells send collaterals to both the prefrontal cortex and striatum. These findings indicate that discrete areas of the amygdala, and in some cases individual amygdaloid neurons, can modulate information processing in the first two links of distinct cortico-striato-pallidal systems arising in the medial and lateral prefrontal cortex.

Afferent Pathways↗
PubMed1991

Topographical organization of amygdaloid projections to the caudatoputamen, nucleus accumbens, and related striatal-like areas of the rat brain.

The topographical organization of amygdaloid projections to the caudatoputamen, nucleus accumbens, and lateral portions of the bed nucleus of the stria terminalis and central amygdaloid nucleus was investigated, in the rat, using the retrograde transport of wheat germ agglutinin-conjugated horseradish peroxidase. Although the caudatoputamen and nucleus accumbens are the principal components of the striatum, there is evidence that lateral portions of the bed nucleus of the stria terminalis and central amygdaloid nucleus may be striatal-like structures. The basolateral nucleus was the main source of amygdaloid fibers to all of these structures. In many instances labeled areas of the basolateral nucleus were continuous with labeled areas in the adjacent lateral and basomedial nuclei. Amygdaloid neurons projecting to the striatum and striatal-like areas exhibited an overlapping topographical organization. In general, the medial-to-lateral coordinate in the striatum corresponds to the medial-to-lateral coordinate in the basolateral nucleus. There was also a partial reversed sagittal topography in that the caudal caudatoputamen receives its principal projection from the rostral basolateral nucleus. However, the rostral basolateral nucleus had a stronger projection to the rostral caudatoputamen and lateral nucleus accumbens than the caudal basolateral nucleus. The principal striatal projection of the caudal basolateral nucleus was to the medial nucleus accumbens. Amygdaloid labeling produced by injections into the medial nucleus accumbens was very similar to that seen with injections into the lateral portions of the bed nucleus of the stria terminalis and central amygdaloid nucleus. The retrograde amygdaloid labeling seen in this investigation, when compared to labeling seen with cortical injections in previous studies, suggests that specific amygdaloid domains project to particular cortical areas as well as to the principal striatal targets of the same areas.

Afferent Pathways↗
PubMed1990

Anatomy of the rat medial geniculate body: II. Dendritic morphology.

The medial geniculate body (MGB) of the rat was studied with Golgi methods to determine the distribution of neurons identified by dendritic morphology. These findings were compared with major divisions and constituent nuclei established by somatic and fiber architectonics, and by connections with temporal neocortex (Clerici et al.: Society of Neuroscience Abstracts 12:1272, 1986; 13:325, 1987; Anatomical Record 218:23, 1987; Winer and Larue: Journal of Comparative Neurology 257:282-315, 1987; Clerici and Coleman: Journal of Comparative Neurology 297:14-31, 1990). It was found that an elaboration of the prototypical scheme proposed by Morest (Journal of Anatomy 98:611-630, 1964) for partitioning the mammalian MGB is valid for characterizing the rat MGB. Two predominant categories of principal neuron dendritic patterning were identified: a bushy cell having tufted dendritic fields and a stellate cell with a radiate dendritic domain. Tufted neurons have large caliber dendritic trunks that divide profusely into daughter branches close to the soma with intertwining higher order branches that maintain a relatively restricted dendritic field. Stellate neurons typically emit primary dendrites in all directions that then divide dichotomously at wide angles at subsequent orders of branching to produce a somewhat spheroidal dendritic field. In the present study, the rat MGB is found to be a tripartite structure composed of ventral (MGv), dorsal (MGd), and medial (MGm) divisions, each uniquely characterized by constituent dendritic morphology. The paramount neuronal class of the MGv is the tufted principal cell. In the ventral and ovoid nuclei of the MGv the neuronal orientation of highly oriented bitufted cells is in register with afferent brachial axons. In the ventral nucleus, this arrangement approximates vertical with a dorsomedial tilt most prominent rostrally; in the ovoid nucleus, tufted cells adhere to the double spiraled course of afferent axons. The transition zone between ventral and ovoid nuclei contains tufted neurons that align with radially oriented fibers issuing from the junction of the ovoid and midgeniculate bundles. Bitufted neurons of the marginal zone parallel fibers at the lateral margin of the geniculate. Within the MGd the dorsal and caudodorsal nuclei are characterized by stellate cells with extensive dendritic arbors and busy neurons with dendritic branches less tufted than those observed in the MGv. The deep dorsal nucleus contains bitufted neurons that polarize with the long axis of the midgeniculate bundle and intermingle with stellate neurons. The suprageniculate nucleus includes neurons with large somata and long, sparsely branched and dorsoventrally oriented dendrites orthagonal to corticothalamic axons, as well as smaller neurons and classical stellate cells.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1990

Social emergencies in the elderly.

An examination of the social concerns of the elderly reinforces the importance of a thorough social assessment and the availability of skilled staff in an Emergency Department to make appropriate community referrals. The resolution of disposition problems brought about through caregiver exhaustion, patients no longer able to care for themselves in the community, and abandonment by individuals and institutions require a complex array of skills. The serious problem of drug and alcohol abuse among the elderly must be recognized by Emergency Department staff. Physical problems often disguise the existence of a problem of substance abuse. Clinicians in the Emergency Department should evaluate elderly patients using social and family history information in addition to a thorough physical assessment. Elder abuse manifests as physical abuse, psychological abuse, material abuse, and active and passive neglect. The problem is growing, and there is a need for skilled observation and detection of elderly patients presenting for emergency care. As the proportion of the elderly population in this country increases, social policies and program development must reflect these changes. Experts in fields such as gerontology, geriatric medicine, psychiatry, nursing, and social work must make recommendations for changes in the medical and social service delivery systems. The availability of coordinated, comprehensive services for the elderly will expand as the movement toward geriatric treatment centers grows. These centers will provide medical, psychiatric, social, and residential care through the concept of a continuum of care. They will employ a multidisciplinary team of geriatric specialists and include outreach as well as treatment services. Communities with a geriatric treatment center provide a valuable resource for patients identified through Emergency Department visits. The Emergency Department must play an active role in assisting hospitals, area agencies on aging, and other concerned members of the community plan programs for elderly patients with physical and social concerns. While these changes are implemented, the Emergency Department will continue to remain responsive to the social concerns of the elderly through deliberate organizational efforts designed to maintain a high quality of care for elderly patients.

Aged↗
PubMed1989

Coexistence of somatostatin with neuropeptide Y, but not with cholecystokinin or vasoactive intestinal peptide, in neurons of the rat amygdala.

A two-color immunoperoxidase procedure was used to determine whether somatostatin (SOM) containing neurons in the amygdala also contain neuropeptide Y (NPY), vasoactive intestinal peptide (VIP), or cholecystokinin (CCK). There was no evidence that SOM-containing neurons in any of the amygdaloid nuclei contain VIP or CCK. In contrast, there was extensive colocalization of SOM and NPY in all of the amygdaloid nuclei with the exception of the intercalated masses and the lateral subdivision of the central nucleus. The greatest number of SOM-NPY double-labeled cells was observed in the medial nucleus, lateral nucleus, and intra-amygdaloid portion of the bed nucleus of the stria terminalis. The morphology of these SOM-NPY neurons was similar in all nuclei. Most exhibited fusiform or ovoid cell bodies with one or two sparsely branched dendrites emerging from each pole of the cell. The extensive coexistence of SOM and NPY in non-pyramidal neurons of the basolateral amygdala is similar to that seen in the cerebral cortex and supports the concept that these brain regions share many important characteristics. The extensive colocalization of SOM and NPY in the medial amygdala, in conjunction with the results of previous studies, suggests that some of these cells may project to the bed nucleus of the stria terminalis and hypothalamus.

Amygdala↗
PubMed1989

Coexistence of GABA and peptide immunoreactivity in non-pyramidal neurons of the basolateral amygdala.

Colocalization of gamma-aminobutyric acid (GABA) immunoreactivity with somatostatin (SOM), neuropeptide Y (NPY), cholecystokinin (CCK), and vasoactive intestinal polypeptide (VIP) immunoreactivity was demonstrated in non-pyramidal neurons of the basolateral amygdala using a two-color immunoperoxidase procedure. Approximately 80-90% of SOM- and NPY-positive neurons in the basolateral amygdala were also immunoreactive for GABA. Virtually all large CCK-positive neurons also exhibited GABA-like immunoreactivity. About one-half of VIP-positive neurons and small CCK-positive cells were also immunoreactive for GABA.

Amygdala↗