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Biomedical subjects

L Medina

Publications and source records attributed to L Medina.

At least 55 records · Page 3Linked to original sources

The efferent connections of the nucleus accumbens in the lizard Gekko gecko. A combined tract-tracing/transmitter-immunohistochemical study.

The present investigation of connections in the basal ganglia of the lizard Gekko gecko has revealed that the efferent projections of the nucleus accumbens are far more elaborate than previously thought. The projections reach not only the ventral pallidum, the preoptic area, the lateral hypothalamic area and the ventral tegmental area, but also the bed nucleus of the stria terminalis, the dorsomedial thalamic nucleus, the substantia nigra and the retrorubral dopaminergic cell group. Additional projections were observed within the nucleus accumbens and, caudally, to the peribrachial region and the superior raphe nucleus. Moreover, the results of the present study indicate that the accumbal projections to both the ventral pallidum and midbrain dopaminergic cell groups have a medial-to-lateral topographical organization. This expanded view of the efferent projections of the nucleus accumbens of Gekko gecko suggests a great resemblance in accumbal output systems between reptiles and mammals. A notable difference, however, is observed in the "limbic loop", which in reptiles, in contrast to mammals, seems to lack a cortical involvement.

Animals↗

Brainstem motoneuron pools that are selectively resistant in amyotrophic lateral sclerosis are preferentially enriched in parvalbumin: evidence from monkey brainstem for a calcium-mediated mechanism in sporadic ALS.

Some brainstem motoneuron groups appear more resistant to the process of neurodegeneration in ALS (for example, oculomotor, trochlear, and abducens nuclei) than others (for example, trigeminal, facial, ambiguus, and hypoglossal nuclei). The possibility that the differential presence of the calcium-chelating protein parvalbumin might underlie this difference in vulnerability was examined immunohistochemically as a way to determine whether a calcium-mediated mechanism might be involved in ALS. In normal monkey brainstem, we found that the abundance of parvalbumin-containing neurons in the oculomotor, trochlear, and abducens nuclei was approximately 90% of the abundance of choline acetyltransferase (CHAT)-containing motoneurons. In contrast, the abundance of parvalbumin-containing neurons in the other brainstem motor nuclei innervating skeletal muscle (trigeminal, facial, ambiguus, and hypoglossal) was only about 30-60% of the abundance of CHAT-containing motoneurons. Since some of these motoneuron pools contain nonmotoneuron internuclear neurons that might be parvalbumin-containing, we also carried out double-label studies to specifically determine the percentage of cholinergic motoneurons that contained parvalbumin in each of these motoneuron pools. We found that 85-100% of the oculomotor, trochlear, and abducens motoneurons were parvalbumin-containing. In contrast, only 20-30% of the trigeminal, facial, ambiguus, and hypoglossal motoneurons were parvalbumin-containing. These results raise the possibility that motoneuron death in sporadic ALS is related to some defect that promotes cytosolic calcium accumulation in motoneurons. This excess calcium entry may promote cell death via an excitotoxic pathway. Motoneurons rich in parvalbumin may resist the deleterious effects of this putative calcium gating defect because they are better able to sequester the excess calcium.

Amyotrophic Lateral Sclerosis↗

Neurotransmitter organization and connectivity of the basal ganglia in vertebrates: implications for the evolution of basal ganglia.

The basal ganglia in modern mammals, birds and reptiles (i.e. modern amniotes) are very similar in connections and neurotransmitters, suggesting that the evolution of the basal ganglia in amniotes has been very conservative. For example, the basal ganglia in all amniotes possess a dorsal striatum containing two main populations of projection neurons, substance P-containing (SP+) and enkephalin-containing (ENK+) neurons, which have major projections to the dorsal pallidum and the tegmentum (ventral tegmental area and substantia nigra, or VTA/SN). The VTA/SN, in turn, has a major dopaminergic (DA+) projection to the striatum in all amniotes. In this paper, we review these data on the basal ganglia in amniotes and note points of similarity and difference in the functional circuitry of the basal ganglia among amniotes. In addition, we review recent findings on the neurotransmitter organization and connectivity of the basal ganglia in amphibians and fishes, with the goal of assessing whether a basal ganglia showing the same basic features as in amniotes is observed in anamniotes. Published data indicate that in at least two groups of fishes (cartilaginous fishes and lungfishes) and apparently in amphibians, the basal ganglia is present and consists of a distinct striatum and pallidum. The striatum of amphibians, cartilaginous fishes, and lungfishes contain SP+ and ENK+ neurons that seem to project to the pallidum as well as to a brainstem cell group that appears comparable to the VTA/SN of amniotes. Data for ray-finned fishes also suggest the presence of a striatum containing SP+ and ENK+ neurons that projects to VTA/SN-like brainstem cell group. In the basal ganglia of ray-finned fishes, however, a distinct pallidum had not been identified. Finally, the brainstem cell group receiving striatal input in all anamniotes contains DA+ neurons that seem to project to the striatum. The present analysis suggests that a rudimentary basal ganglia was already present in the brain of the ancestral jawed vertebrates. This rudimentary basal ganglia likely consisted of a striatum and a pallidum, and the striatum probably already possessed the same basic connections and some of the same basic cell types as the basal ganglia of modern jawed vertebrates.

Animals↗

Development of catecholamine systems in the brain of the lizard Gallotia galloti.

For a better insight into general and derived traits of developmental aspects of catecholaminergic (CA) systems in amniotes, we have studied the development of these systems in the brain of a lizard, Gallotia galloti, with tyrosine hydroxylase (TH)- and dopamine (DA) immunohistochemical techniques. Two main groups of TH-immunoreactive (THi) perikarya appear very early in development: one group in the midbrain which gives rise to the future ventral tegmental area, substantia nigra and retrorubral cell groups, and another group in the tuberomammillary hypothalamus. Somewhat later in development, TH/DA-immunoreactive cells are observed in the thalamus, rostrodorsal hypothalamus and spinal cord, and, with another delay, in the suprachiasmatic nucleus, the periventricular organ, and the pretectal posterodorsal nucleus. CA cell groups that appear rather late in development include the cells in the olfactory bulb, the locus coeruleus and the caudal brainstem. As expected, the development of immunoreactive fibers stays behind that of the cell bodies, but reaches the adult-like pattern just prior to hatching. The present study revealed considerable variation in the relation between the state of cytodifferentiation and first expression of TH/DA immunoreactivity between CA cell groups. Catecholamine cells in the midbrain and tuberomammillary hypothalamus are still migrating, immature (absence of dendrites) and express only TH immunoreactivity at the time of first detection. Cells which appear at later developmental stages lie already further away from the ventricle, possess two or more dendritic processes, and generally express both TH- and DA immunoreactivity.

Animals↗

Leukotriene C4 upregulates collagenase expression and synthesis in human lung fibroblasts.

Leukotriene C4 (LTC4), a mediator generated by a variety of inflammatory cells, participates in several physiological and pathological processes. It has been shown that LTC4 stimulates collagen synthesis by fibroblasts, suggesting a role in collagen turnover. However, the possible effect of this mediator on collagen degradation has not been examined. In this study we explored the role of LTC4 in the modulation of fibroblast interstitial collagenase and TIMP-1. Confluent cultures of three human normal lung fibroblast cell lines, and one derived from idiopathic pulmonary fibrosis (IPF) were exposed to LTC4 0.1, 1 and 10 nM, and to IL-1 beta as positive control. Collagenase and TIMP mRNAs expression were analyzed by Northern blot followed by densitometric scanning. Immunoreactive procollagenase was detected by immunoblot, and collagenase activity was measured using [3H]collagen. Our results showed that LTC4 enhanced several-fold collagenase mRNA expression in collagenase-producing fibroblasts, and induced the expression of the enzyme mRNA in collagenase-nonproducing fibroblasts, both in normal and IPF derived cell lines. LTC4 1 nM induced the highest response. Collagenolytic activity and immunoreactive collagenase paralleled collagenase mRNA expression. Interestingly, simultaneous exposure of fibroblasts to LTC4 plus IL-1 failed to show additive effects. Moreover, in two cell lines the combination resulted in a decrease of collagenase mRNA expression compared with both mediators separately. TIMP mRNA levels were not significantly modified by LTC4, nor IL1 beta. Our findings suggest that LTC4 plays a role in the modulation of fibroblast collagenase, and it may participate in extracellular matrix remodeling during lung inflammation.

Collagenases↗

Distribution of choline acetyltransferase immunoreactivity in the pigeon brain.

We have investigated the distribution of cholinergic perikarya and fibers in the brain of the pigeon (Columba livia). With this aim, pigeon brain sections were processed immunohistochemically by using an antiserum specific for chicken choline acetyltransferase. Our results show cholinergic neurons in the pigeon basal telencephalon, the hypothalamus, the habenula, the pretectum, the midbrain tectum, the dorsal isthmus,the isthmic tegmentum, and the cranial nerve motor nuclei. Cholinergic fibers were prominent in the dorsal telencephalon, the striatum, the thalamus, the tectum, and the interpeduncular nucleus. Comparison of our results with previous studies in birds suggests some major cholinergic pathways in the avian brain and clarifies the possible origin of the cholinergic innervation of some parts of the avian brain. In addition, comparison of our results in birds with those in other vertebrate species shows that the organization of the cholinergic systems in many regions of the avian brain (such as the basal forebrain, the epithalamus, the isthmus, and the hindbrain) is much like that in reptiles and mammals. In contrast, however, birds appear largely to lack intrinsic cholinergic neurons in the dorsal ("neocortex-like") parts of the telencephalon.

Animals↗

Distribution of choline acetyltransferase immunoreactivity in the brain of the lizard Gallotia galloti.

The aim of the present study is to provide a complete description of the distribution of choline acetyltransferase (ChAT) immunoreactivity (i) in the brain of the lizard Gallotia galloti, on the basis of two different primary antisera: rat anti-ChAT and rabbit anti-chicken ChAT. Considering that the brain is a segmented structure, we have analysed our data with respect to transverse segmental domains (or neuromeres), which have been previously described by several authors in the brain of vertebrates. In the telencephalon, ChATi neurons are seen in the cortex, anterior dorsal ventricular ridge, basal ganglia, diagonal band, and bed nucleus of the stria terminalis. Further caudally, ChATi cell bodies are located in the preoptic area, hypothalamus, habenula, isthmus, and all motor efferent centers of the brainstem and spinal cord. Plexuses of ChATi fibers are observed in the areas containing cholinergic cell bodies. In addition, distinct plexuses are found in the cortex, the posterior dorsal ventricular ridge, the neuropiles of all primary visual centers of the diencephalon and mesencephalon, and several non-visual nuclei of the brainstem. The distribution of ChAT immunoreactivity in the brain of G. galloti resembles in many respects that of other vertebrates, and differences are mainly observed in the pretectum and midbrain tectum. Transverse segmental domains were identified in the brainstem and forebrain of Gallotia when the cranial nerve roots and fiber tracts were used as a reference, and most cranial motor nuclei were found to occupy the same segmental positions as have been reported in the chick.

Animals↗

Distribution of neuropeptide Y-like immunoreactivity in the brain of the lizard Gallotia galloti.

The distribution of neuropeptide Y (NPY)-like immunoreactivity was studied in the brain of the lizard Gallotia galloti, in order to gain insight into the comparative topography of this peptide. Antisera against both NPY and its C-terminal flanking peptide (C-PON) were used, demonstrating a general coexistence of both peptides, as described in other vertebrates. Most NPY-like immunoreactive (NPY-LI) cell bodies were observed in the telencephalon, specifically in various olfactory structures, all cortices, septum, basal ganglia (except for the globus pallidus), the nucleus of the diagonal band of Broca, the amygdaloid complex, and the bed nucleus of the anterior commissure. NPY-LI cells were also seen in the preoptic and hypothalamic regions and the dorsal thalamus (mainly in the perirotundal belt), as well as in the mesencephalic tegmentum (in the ventral tegmental area, the substantia nigra, and the retrorubral area). NPY-LI fibers and terminals were widely distributed in the brain. All visual and auditory neuropiles were densely innervated. Specially dense plexuses were seen in the nucleus accumbens, the ventral pallidum, the suprachiasmatic and ventromedial hypothalamic nuclei, the nucleus medialis thalami, the left habenula, and the central nucleus of the torus semicircularis. Our analysis shows that the distribution of NPY-like immunoreactivity in the forebrain of Gallotia largely resembles that of other vertebrates, whereas differences are mainly observed in the brainstem. The widespread distribution of NPY in the lizard brain suggests several modulatory functional roles, either in local-circuit systems of the forebrain, or in various limbic, neuroendocrine, and sensory pathways.

Animals↗

Cholinergic, monoaminergic and peptidergic innervation of the primary visual centers in the brain of the lizards Gekko gecko and Gallotia galloti.

In order to study the relationship between retinal projections and immunohistochemically identified neurotransmitter systems in the primary visual centers of the brain in lizards, intraocular injections of horseradish peroxidase were combined with immunohistochemistry. Antibodies raised against six substances were applied: choline acetyltransferase (ChAT), serotonin (5-HT), tyrosine hydroxylase (TH), dopamine (DA), substance P (SP), and leu-enkephalin (LENK). In the primary visual centers of the lizards Gekko gecko and Gallotia galloti, notable overlap was observed between retinofugal fibers with: 1) ChAT-immunoreactive fibers in almost all primary visual centers; 2) 5-HT-immunoreactive fibers in the ventral lateral geniculate body and the basal optic nucleus; 3) TH-immunoreactive fibers in the nucleus ovalis and the dorsal lateral geniculate body; 4) SP- and LENK-immunoreactive fibers in the perirotundal belt; and 5) TH- and SP-immunoreactive fibers in the pretectal posterodorsal nucleus. The latter nucleus also contains dopaminergic cell bodies that lie outside the retinal target area but have dendrites extending into it. Several differences were noted in the distribution of 5-HT, TH-, DA-, and LENK-immunoreactive fibers in the tectum of the midbrain in the two species studied. Distinct laminae of 5-HT-immunoreactive fibers (layer 9) and TH- and DA-immunoreactive fibers (layers 9 and 11) are present in G. gecko but absent or, at least, less distinct in G. galloti. On the contrary, the optic layers in the tectum of G. galloti show a rather dense plexus of LENK immunoreactive fibers, whereas the corresponding layers in G. gecko are devoid of LENK-immunoreactivity. Since only a very few ChAT immunoreactive fibers were observed in the optic nerve of G. galloti, most of the observed immunoreactive fibers in the primary visual centers are considered to have an extraretinal origin. Putative sources of the cholinergic, the monoaminergic, and the peptidergic innervation of the primary visual centers in reptiles include the isthmic nucleus, the raphe nuclei, the substantia nigra and the nucleus of the posterior commissure, as reported in other amniotes.

Animals↗

Comparative aspects of the basal ganglia-tectal pathways in reptiles.

To determine how the basal ganglia in reptiles may influence visuomotor behavior, the connections from the basal ganglia to the tectum of the midbrain were studied in several species of reptiles. Immunohistochemical studies by means of antibodies against Leu-enkephalin (LENK) as well as experimental hodological studies with anterograde (PHA-L) and retrograde (HRP, Fluorogold, Cholera toxin) tracers were carried out. The results indicate that within the class of Reptilia, two different patterns occur: one in which information from the basal ganglia is relayed to the tectum via the substantia nigra as well as via a pretectal, enkephalinergic cell group, and another one in which only the ventral route, via the substantia nigra, is present. The former pattern is found in turtles, crocodiles, and the lacertid lizards Podarcis and Gallotia, and the latter pattern in the gekkonid lizards Gekko and Eublepharis, in Varanus, and in the snakes Python and Thamnophis. The presence or absence of the pretectal relay center is reflected in the laminar distribution of LENK immunoreactivity in the tectum. The apparent lack of a pretectal relay in nocturnal gekkonids and in snakes underlines the hypothesis (Reiner et al., '84: T.I.N.S. 7:320-325) that a de-emphasis of visual-basal ganglia mechanisms has occurred during the evolution of ancestral reptiles to modern mammals.

Animals↗

Phenanthrylalkanoic acids, IV: Syntheses and antiinflammatory activity of 2-, 3-, and 9-phenanthryl- and 9-chloro-3-phenanthryl derivatives of propanoic acid.

The phenanthrylethanols 2a-d were obtained by reduction of the acetyl derivatives 1a-d and converted, through the phenanthrylethyl halides 3a-d and 4b, into the nitriles 5a-d, whose acid hydrolysis afforded the acids of the title, 6a-d. The antiinflammatory activity of these acids was measured on the carrageenin-induced edema and found as 1/3 (6a), 1/43 (6b), 1/5 (6c), and 1/7 (6d) of that of fenbufen.

Animals↗

MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.

MR studies were correlated with biochemical results in nine children who presented with lactic acidosis and/or abnormal MR findings in the basal ganglia. Neurologic development was delayed in all nine children. Seven of these patients were diagnosed as having subacute necrotizing encephalomyelopathy (SNE, or Leigh syndrome) on the basis of history, clinical findings, and biochemical studies; of the remaining two, one had congenital lactic acidosis and the other had familial bilateral striatal necrosis with no known biochemical correlate. Although the clinical presentation of these patients was similar, we found distinctive MR abnormalities in characteristic locations in the seven patients with SNE, with or without detectable specific mitochondrial enzyme deficiency in cultured skin fibroblast assays. In our case studies of SNE patients with detectable enzyme deficiency states, defects in pyruvate dehydrogenase complex and cytochrome c oxidase have been found. The MR finding of note in SNE is the remarkably symmetrical involvement, most frequently of the putamen. In our study, lesions were also commonly found in the globus pallidus and the caudate nucleus, but never in the absence of putaminal abnormalities. Other areas of involvement included the paraventricular white matter, corpus callosum, substantia nigra, decussation of superior cerebellar peduncles, periaqueductal region, and brainstem. In patients who present with lactic acidosis and whose MR findings show symmetrical abnormalities in the brain, but with sparing of the putamen, the diagnosis of SNE is in doubt.

Acidosis, Lactic↗

The various scintigraphic patterns of Warthin's tumor.

The authors' experience with salivary gland imaging in patients with Warthin's tumor was reviewed and the scans correlated with the pathologic findings of each tumor in an attempt to explain the scintigraphic variants found. Most Warthin's tumors show increased perfusion on imaging. The predischarge static images have a low sensitivity, detecting only 33% of the tumors. Warthin's tumors may appear hot, warm, or cold on the predischarge images but invariably become hot in the postdischarge study, for a 100% sensitivity. Many tumors reveal internal warm or cold areas. These focal defects correlate well with the presence of intratumoral cysts. The presence of these mixed lesions should not lead the physician away from the diagnosis of Warthin's tumor.

Adenolymphoma↗

[Hepatic laparoscopy and biopsy in the diagnosis of hepatic cirrhosis].

316 cases of proved hepatic cirrhosis (HC) which underwent Laparoscopy (L) were analysed. In 94 cases, hepatic biopsy by needle (HBN) was also practised under laparoscopic view, 96 cases were controlled until death, with a follow-up of almost 90 months. In 54 of these, there is a complete necropsy study. The performance in diagnosis of cirrhosis, L and HBN are compared separately. L gave the exact result of 96.6% and HBN 74.7%. HBN commonly practised with a Menghini needle (1.2 or 1.4 mm) as it is one that produces less complications, gives and insufficient sample, which determines that in 25.3% of the cases under biopsy, the HC diagnosis could not be proved, while L only fails in this aspect, in 3.38%. To this disadvantage of HBN, we must add another negative factor, the frequency which HBN can not be practised due to prothrombin under 50%, which nevertheless is not an obstacle for practising an L. In this series we have not reported any deaths with this two techniques. L has the additional advantage to contribute other useful data which can not be obtained with HBN alone. as revealing signs of portal hypertension, and hepatobiliary or peritoneal pathology which can coexist with HC. Due to this reasons, in the study of HC, we preferred as the first method of diagnosis, L, instead of HBN. When through this endoscopy we obtain the typical aspect, we omit adding HBN, which we only practised in doubtful cases of not very nodular livers (glabra cirrhosis) or when a probable post-hepatis, Wilson disease or hemochromatosis is being investigated. In the present conditions, we believe that the new methods of diagnosis "of non invasive images" can not substitute L or HBN in precising the diagnosis of HC.

Biopsy, Needle↗