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1.
Histol Histopathol ; 18(3): 855-69, 2003 07.
Article in English | MEDLINE | ID: mdl-12792898

ABSTRACT

Dystrophic calcification of previously damaged areas of nervous tissue occurs in a wide range of human diseases. The relationship between astroglial and microglial reactions and deposits of calcium salts was studied for up to five months in rats with a brain lesion produced by systemic administration of kainate. The morphology and atomic composition of the calcium salt deposits was also studied. Two types of lesions, sclerotic and liquefactive, were observed. In sclerotic lesions hyperplasia and hypertrophy of astrocytes partially substituted for the lost neurons, reaching a maximum in about twenty-five days after treatment. In liquefactive lesions, the astrocytic reaction occurred only around the liquefactive area. Microglial reaction was similar in both types of lesion and reached its highest expression in about twenty-five days. Calcium deposits were observed in the sclerotic but not in the liquefactive lesions. Clearly distinguishable granules of calcium salts were observed in sclerotic lesions under scanning electron microscopy after only five days post-injection. The size of calcified granules increased with time reaching 40 micro m or more in diameter at five months. The atomic composition of these deposits, studied by X-ray microanalysis, showed a time-dependent increase in calcium concentration. While there was no clear relationship between astroglial and microglial reactions and calcium salt deposits, the systemic injection of kainate produced progressively larger and more concentrated calcium deposits in sclerotic, but not in liquefactive lesions.


Subject(s)
Brain Injuries/chemically induced , Brain/metabolism , Kainic Acid/administration & dosage , Animals , Astrocytes/metabolism , Brain/pathology , Calcium/metabolism , Excitatory Amino Acid Agonists/administration & dosage , Glial Fibrillary Acidic Protein/metabolism , Kainic Acid/metabolism , Lectins/metabolism , Male , Microglia/metabolism , Neurons/metabolism , Rats , Rats, Wistar , Time Factors
2.
Brain Res Dev Brain Res ; 122(1): 35-46, 2000 Jul 30.
Article in English | MEDLINE | ID: mdl-10915903

ABSTRACT

To establish if olfactory bulb sensitivity to functional deprivation is related to the degree of development at birth, we studied the effects of surgical closure of one naris in the gerbil olfactory bulb development. The naris closure was performed at three different ages: at birth, P7 and P14 and maintained for 30 or 60 days. In coronal sections we measured total bulbar surface area and surface area of the different bulbar layers establishing an estimate multiple regression model for the percentage of surface area decrease in the deprived bulb related to non deprived one. The internal and external plexiform layers are the most sensitive layers to deprivation and age and duration of deprivation were factors in their mathematical models. The glomerular layer showed a surface reduction of about 25% without dependence either on age or duration. The deprived glomerular layer showed a much lower tyrosine hydroxylase-immunoreactivity and immunoreactive cell density than those in the non deprived one. However, differences in calbindin-immunoreactive and NADPH-diaphorase positive cell density between deprived and non deprived glomerular layer were not significant. Our results indicate that olfactory bulb sensitivity to functional deprivation is not related to the degree of precocity and changes in age and duration of deprivation cause different effects on the olfactory bulb layers.


Subject(s)
Functional Laterality/physiology , Gerbillinae/physiology , Olfactory Bulb/growth & development , Sensory Deprivation/physiology , Animals , Animals, Newborn , Calbindins , Female , Male , NADPH Dehydrogenase/analysis , Neuronal Plasticity/physiology , Nose/surgery , Olfactory Bulb/cytology , Olfactory Bulb/physiology , Olfactory Receptor Neurons/chemistry , Olfactory Receptor Neurons/enzymology , S100 Calcium Binding Protein G/analysis , Smell/physiology , Species Specificity , Tyrosine 3-Monooxygenase/analysis
3.
Histol Histopathol ; 13(4): 927-37, 1998 10.
Article in English | MEDLINE | ID: mdl-9810485

ABSTRACT

Experimental structural dextroconvex scoliosis was produced in rabbits by costotransversolisis with transversectomy and releasing of paravertebral muscles between TVII and TX on the right side. Two compensatory curves developed on the upper dorsal and lumbar levels. Biopsies of paravertebral muscles in experimental animals included, besides areas of normal tissue, a considerable derangement of the cell contractile apparatus with sarcoplasmic dilation and eventual cell disintegration and necrosis. Histological changes varied along levels, the convexity being more affected. The severity of changes and reduction in body weight and length were correlated with the degree of scoliosis. A selective atrophy of slow-twitch fibers was observed in experimental animals, especially at the level of the main curve, whereas fast-twitch fiber atrophy was more important caudally. Control animal biopsies always appeared normal. Our experimental model shows an overt participation of paravertebral muscles in the establishment of compensatory processes following scoliosis, although the role that paravertebral muscles play in the etiopathogenesis of human idiopathic scoliosis requires further investigation.


Subject(s)
Muscle, Skeletal/pathology , Scoliosis/pathology , Animals , Disease Models, Animal , Female , Male , Muscle, Skeletal/ultrastructure , Rabbits , Radiography , Scoliosis/diagnostic imaging , Spine/diagnostic imaging
4.
Brain Res ; 653(1-2): 92-100, 1994 Aug 08.
Article in English | MEDLINE | ID: mdl-7982081

ABSTRACT

The relationship between hippocampal damage and spatial learning deficiencies was studied in rats injected with kainic acid (10 mg/kg i.p.). A single injection was given either before or after the acquisition phase of the Morris water-maze task. In this acquisition phase, the animals were required to find a hidden underwater platform starting from four different points. The task was repeated twice a day for 10 days. In the retention phase after 10 days rest, the rats repeated the same task. The damage caused by the treatment occurred in several prosencephalic areas, including the piriform and enthorhinal cortices, the thalamus and the hippocampus. In the latter, greatest damage was seen in CA1 followed by CA3 while CA2 and the gyrus dentatus appeared almost unaffected. The behavioural results indicated that kainic acid impaired but did not preclude the acquisition of the water-maze task. During the retention phase, no significant differences in latencies were found between animals that were treated before and after acquisition, thus, indicating that pretraining does not play an important role in the recovery of these spatial abilities following hippocampal lesions.


Subject(s)
Brain/drug effects , Kainic Acid/pharmacology , Learning/drug effects , Motor Activity/drug effects , Animals , Brain/metabolism , Brain/pathology , Brain Mapping , Glial Fibrillary Acidic Protein/metabolism , Immunohistochemistry , Injections, Intraperitoneal , Male , Rats , Rats, Wistar , Reaction Time/drug effects , Retention, Psychology/drug effects
5.
Acta Otorrinolaringol Esp ; 42(6): 465-71, 1991.
Article in Spanish | MEDLINE | ID: mdl-1790070

ABSTRACT

Utilizing 26 Wistar albino rats, an anterograde and retrograde study has been performed on the connections between the first neuron of the olfactory pathway located in the olfactory epithelium and the second neuron in the glomeruli of the bulb. In the experiment we used horse radish peroxidase (HRP) in free form and combined with wheat lectin. In anterograde transport (epithelium-bulb), the HRP is deposited in preestablished sites in the olfactory epithelium of the nasal fossa. In retrograde transport (bulb-epithelium), HRP combined with wheat lectin is injected by means of a Hamilton microsyringe, glass micropipette and stereotaxic apparatus, in foreseen sites of the glomerular layer of the bulb.


Subject(s)
Axons/metabolism , Horseradish Peroxidase/metabolism , Olfactory Bulb/metabolism , Olfactory Mucosa/metabolism , Smell , Animals , Rats , Rats, Inbred Strains
6.
Brain Res Dev Brain Res ; 57(1): 43-53, 1990 Dec 01.
Article in English | MEDLINE | ID: mdl-1708707

ABSTRACT

This paper deals with the postnatal development of afferent and efferent connections of the rat striatum as revealed by the transport of horseradish peroxidase conjugated with wheat germ agglutinin (WGA-HRP). Tracer was injected weekly from birth to the end of the first postnatal month in the head of the caudate nucleus. To control for transport from cortical areas contaminated by the micropipette, injections in newborn rats were made by either vertical or lateral penetrations. In addition some newborn and 14-day-old animals were injected only in the cortex. The results showed that at birth there was retrograde transport to the thalamus, substantia nigra and raphe nuclei. Labelling in the cortex was seen at birth but was probably due to cortical contamination. Transport from the striatum was clearly established on day 7, when a few labelled neurons were observed on both the ipsi and contralateral sides. These neurons increased in number and were distributed through layers III to VI by day 14. At this time labelled cell bodies were observed in the claustrum and lateral amygdaloid nucleus as well as in the globus pallidus and entopeduncular nucleus. On day 21 the contralateral labelling of the lateral amygdaloid nucleus was apparent. The anterograde transport from the striatum to globus pallidus, entopeduncular nucleus and substantia nigra was already visible at birth although its intensity increased during the first postnatal month.


Subject(s)
Corpus Striatum/growth & development , Aging/physiology , Animals , Animals, Newborn/physiology , Biological Transport, Active , Corpus Striatum/anatomy & histology , Corpus Striatum/metabolism , Horseradish Peroxidase , Neural Pathways/physiology , Neurons, Afferent/physiology , Neurons, Efferent/physiology , Rats , Rats, Inbred Strains , Stereotaxic Techniques , Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate , Wheat Germ Agglutinins
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