A swift response to a "modest" proposal.
Explore the source record for details and available documents.
Clinical Trials as Topic↗
Biomedical subjects
J L Cova
Publications and source records attributed to J L Cova.
Synaptic detachment from hypoglossal neurons after different types of nerve injury in the cat.
Quantitative electron microscopy was used to examine synaptic numbers and total relative synaptic coverage on hypoglossal neuronal perikarya following transection or crush of the hypoglossal nerve in the cat. In cats subjected to nerve transection there was a statistically significant decrease in total synaptic coverage as well as in number of synaptic contacts/soma profile. After nerve crush there was a statistically significant decrease in total synaptic coverage but not in the number of synaptic contacts. These results indicate that the degree of synaptic detachment on motor neurons in the cat is influenced by the type of nerve injury.
Animals↗
Changes in microglial cell numbers in the spinal cord dorsal horn following brachial plexus transection in the adult rat.
The effect of peripheral nerve transection on the size of the microglial cell population in cytoarchitecturally distinct regions of the spinal cord dorsal horn of rats was evaluated at selected intervals 2 through 35 days after unilateral brachial plexotomy. The identification of cells was verified by electron microscopic examination of a representative random sample of cells included in the counts. Microglial cell numbers were increased in laminae I, II as well as the arbitrarily defined deeper laminae 3.5 days after surgery. Although microglial cell numbers in laminae I were within normal range 35 days after axotomy, those of the more ventrally located laminae remained significantly greater than control values for the duration of the experimental period. These findings demonstrate that: 1) microglial cell proliferation in the dorsal horn is an early event in the central changes that are attendant to peripheral nerve injury 2) the time course of the response varies in cytoarchitecturally different regions.
Animals↗
Effect of axotomy on perineuronal glial cells in the hypoglossal and dorsal motor vagal nuclei of the cat.
An approximate twofold increase in microglial cell densities occurred in the hypoglossal and dorsal motor vagal nuclei of the cat after transection of their respective nerves. The densities of astrocytes and oligodendrocytes were unaffected. A significant loss of neurons was demonstrated in both nuclei. These findings indicate that a perineuronal microglial cell reaction occurs in craniomotor nuclei of the cat following nerve transection, but to a considerably lesser extent than in rats and rabbits. We suggest that the different glial response after nerve transection compared with nerve crush in the cat may be related to differences in the degree of axotomy-induced neuronal degeneration.
Animals↗
A morphological study of glial cells in the hypoglossal nucleus of the cat during nerve regeneration.
The cat hypoglossal nerve and nucleus have been used as a model for the study of the occurrence and time course of modifications in the size and composition of the perineuronal glial cell population as they relate to cytological changes in the nerve cell body and the initiation and progress of axon regeneration. Animals were killed at 2, 5, 10, 20, 35, 65, and 115 days after crush injury to the hypoglossal nerve. At 5 days after surgery, growth cones and regenerating unmyelinated axons were present at the lesion site, but no conspicuous changes were apparent in the nerve cell bodies. At 10 days after surgery, the granular endoplasmic reticulum was disaggregated and depleted. The elongation phase appeared to be completed at 20 days, as judged by the bilateral retrograde labeling of the hypoglossal nuclei with horseradish peroxidase. By 35 days, the cytoarchitecture of the nerve cell bodies and maturation of axons, as determined by a comparison of the relative frequency distribution of cross sectional areas proximal and distal to the lesion, were completely restored. Comparative quantitative light microscopic examination of the hypoglossal nuclei of intact and experimental animals failed to reveal any statistically significant differences in the total number of glial cells, number of glial cells/unit area of neuropil, or relative proportions of glial cell types at any of the postoperative time intervals. Moreover, electron microscopic quantitation of the microglial cell population did not reveal any significant alterations in the number, density, location, or morphology of these cells.(ABSTRACT TRUNCATED AT 250 WORDS)
Animals↗
Pigmented cells in the leptomeninges of the cat.
Cells laden with pigment granules are described in the leptomeningeal tissues of the cat and kitten. These cells can be identified consistently by gross observation following vascular perfusion. The fusiform or stellate pigmented cells are most often found in association with the outermost layers of the arteries of the subarachnoid space. They are typically separated from the cerebrospinal fluid by an attenuated layer of pial cells. Vessels that are described as having pigmented cells along their course are the anterior and posterior cerebellar; the anterior, middle, and posterior cerebral; and the basilar. Electron microscopic studies confirm the presence of abundant pigment granules. The pigment granules are the predominant component of the cytoplasm. Few organelles are demonstrable except for a large central nucleus. The data provide support for the concept of neural crest contribution to leptomeningeal structures. Identification of this isolated, easily defined population of melanocytes may provide a model for further studies of neural crest distribution as well as experimental approaches to melanogenesis and melanoma production and control.
Animals↗
Effect of nerve section on perineuronal glial cells in the CNS of rat and cat.
The effect of axotomy on the numbers and density of perineuronal cell populations was evaluated in rats, cats and kittens. Cats were sacrificed at different postoperative time intervals two through 90 days after unilateral plexotomy. Kittens (6-10 weeks of age) were subjected to the same surgical procedure and sacrificed one through 28 days after surgery. Rats were sacrificed 10 and 15 days after unilateral section of the brachial plexus or at 7 or 10 days after section of the left hypoglossal nerve. A marked increase in the total number and density of perineuronal cells occurred in the rat ventral horn 10 and 15 days after axotomy. A similar response was noted in the rat hypoglossal nucleus 7 and 10 days after neurotomy. In contrast, no significant change in these parameters was observed in the ventral horns of cats and kittens at any of the postoperative time intervals. Although quantitatively demonstrable increases in the perineuronal cell populations occur in the ventral horns and hypoglossal nuclei of rats, similar modifications do not occur in the cat following axon injury. These findings suggest that evolutionary modifications may have occurred in how perineuronal glia respond to peripheral axon injury.
Animals↗
Uptake of tritiated leucine by axotomized cervical motoneurons: an autoradiographic study.
Explore the source record for details and available documents.
Animals↗
Quantitative cytochemistry of RNA in axotomized feline rubral neurons.
One-sided lateral funiculotomy at the C-2 segment induced axon reaction in the contralateral red nucleus of adult cats. Two to 60 days postoperatively the animals were sacrificed and the mesencephalon was fixed in ethanol-acetic acid, 3:1. Ten micrometer paraffin sections including both red nuclei were stained for RNA with azure B after incubation in DNAse. Cytophotometric measurements of RNA content of neurons from the caudal 600-1000 micrometer of each red nucleus were made with a Zeiss Cytoscan system using an automatic scanning stage. In contrast to the heightened RNA synthesis that has been reported for axotomized peripheral (extrinsic) neurons, the axotomized central (intrinsic) neurons of the red nucleus showed no evidence of accumulation of cytoplasmic or nucleolar RNA. Rather depletion of cellular RNA occurred. Further indication of the regressive nature of rubral axon reaction derived from morphometric measurements that showed cytoplasmic, nuclear and nucleolar atrophy of the neurons of the red nucleus contralateral to operation with the exception of a possible transient cytoplasmic enlargement 9 days postoperatively. From the cytophotometric and morphometric data here reported we are led to suggest that the frequently observed failure of axonal repair in mammalian CNS results from the innately regressive nature of the axon reaction of many mammalian central neurons.
Afferent Pathways↗
Quantitative relationships of the fourth complement component in human cerebrospinal fluid.
A technique for the measurement of cerebrospinal fluid C4 concentration in unconcentrated specimens has been developed with the methods of electroimmunodiffusion and immunofixation. The method has proved to be reproducible and requires only microliter volumes of undiluted cerebrospinal fluid (CSF). The mean value for CSF C4 concentrations in 16 neurologically normal individuals was 325 +/- 32 mug/100 ml. A positive correlation between CSF C4 concentration and the concentration of CSF albumin and total protein was observed. The positive correlation between the concentrations of CSF C4 and albumin was, however, more clearly defined than the relationship of CSF C4 to total CSF protein.
Albumins↗