Effects of aging and food restriction on the trigeminal ganglion: a morphometric study.

A quantitative morphometric study of the rat trigeminal ganglion was conducted to determine the changes that occur with aging. All measurements were tracked from young to old age in two rat groups simultaneously. One group was fed ad libitum, the other was maintained on restricted food intake from 6 weeks on. Immunocytochemical and radioimmunoassay techniques were used to study the neuron group that produces the peptide, CGRP and to compare it with the CGRP-negative neuron group. We observed that in the trigeminal ganglion, soma diameters and nucleus diameters of all neurons, whether CGRP positive or negative, increased modestly with age; so did total ganglion weight. Food restriction delayed, but did not prevent the increases in neuron diameters. No significant changes occurred as a function of age in the total number of neurons per ganglion, the ratio of CGRP positive to CGRP negative neurons and ganglion content of CGRP. Food restriction did not affect the parameters that remained constant with age. These findings are in contrast to the marked inhibitory effect of food restriction on age-related increase in thyroid calcitonin, a hormone that is encoded by the same gene as CGRP.

Pyramidal tract of the cat: axon size and morphology.

The purpose of this work was to determine the number and morphology of pyramidal tract (PT) axons in the cat, using electron microscopy, modern methods of fixation, and computer-assisted morphometric analysis. Sections taken at the level of the medullary pyramids in three animals were fixed and magnified up to 10,000 X to produce photomicrographs. Morphological data were entered into computer files for analysis by tracing axon perimeters on micrographs mounted on a digitizer tablet. The number of axons per PT averaged 415,000, of which 88% were myelinated and 12% were unmyelinated. 90% of the myelinated axons fell in the diameter range 0.5-4.5 microns. Axons larger than 9 microns diameter accounted for 1% of the total; the largest were 20-23 microns. Myelinated axon mean diameter was 1.98 microns; because of the skewed distribution, with many small axons and a few very large axons, median diameter was 1.60 micron. Size distribution was relatively uniform throughout the PT cross section, with all sizes represented in all regions. However, the more medial regions had a higher proportion of small fibers than the more lateral regions: mean medial diameter was 1.85 micron while mean lateral diameter was 2.09 microns. Myelin sheath thickness averaged 7.9% of fiber diameter for axons up to 11 microns, but was constant at 0.9 micron for larger fibers. Myelinated fibers were distorted from the circular shape in cross section, with a mean circularity index (or form factor) of 0.85, which implies that the fibers could swell about 15% without rupture of the cell membrane.(ABSTRACT TRUNCATED AT 250 WORDS)

Unmyelinated axons in the pyramidal tract of the cat.

Ultrastructural preparations revealed the presence of unmyelinated axons in the pyramidal tract (PT) of the adult cat. At the level of the medulla oblongata, unmyelinated axons constituted 8-15% of the total PT population. Axon diameters ranged from 0.05 to 0.06 micron with a mean of 0.18 micron. Although axons were distributed throughout the PT, their density was highest in the medial part.

Origin of the pyramidal tract determined with horseradish peroxidase.

The origin of the axons contained in the pyramidal tract (PT) of the cat was established using retrograde transport of horseradish peroxidase (HRP). A complete section was made through a PT at the level of the medulla oblongata and HRP was applied to the sectioned axons. Cat brains were cut in frontal and sagittal planes and HRP-labeled cells were plotted in outlines of the brain sections. The entire cortical region containing PT cells was divided into 8 subregions and the percent of PT cells was determined in each. Surface cortex, subregions 1, 3 and 8, contained only 30--40% of PT cells; the majority resided in deep sulcal cortex, in subregions 2, 4, 5, 6 and 7. Subregion 1 (containing 6--12% of PT cells) extends rostral to the cruciate sulcus; subregion 3 (15--22%) extends from the cruciate sulcus caudally to the ansate sulcus; subregion 8 (7--8%) covers cortex laterally adjacent to subregion 3. The hidden banks of the cruciate sulcus contained the greatest concentration of PT cells, 28--34% in the dorsal bank (subregion 5) and 15--20% in the ventral bank (subregion 4). The coronal sulcus contained only 2--5% of PT cells in its dorsal bank (subregion 6) and 1--4% in its ventral bank (subregion 7). The presylvian sulcus contained 8--12% of all PT cells in its lateral bank (subregion 2). This new cortical area is not yet considered part of 'PT cortex'. Qualitative limitations of this study are discussed.

Tooth pulp-driven neurons in somatosensory cortex of primates: role in pain mechanisms including a review of the literature.

The tooth pulp of primates was stimulated electrically while searching for evoked unit potentials in the cerebral cortex. Control procedures were employed to assure that the electrical stimuli reached only tooth pulp fibers but no extrapulpal sensory fibers. In addition, an electrode was inserted in soft tissue surrounding the tooth for separate excitation of extrapulpal axons. A tooth pulp projection area was identified in the "face area" of primary somatosensory cortex. Two major neuron groups were encountered, one excited only by the extrapulpal soft tissue stimulus, the other by tooth pulp stimuli. Within the pulp-projection area, soft tissue-driven neurons were most numerous in superficial cortex of the postcentral gyrus, pulp-driven neurons dominated in deep cortex in the base of the central sulcus. The pulp-driven population divided into several functional subsets: those excited from one pulp only (conceivably capable of localizing pulpal stimuli), those excited from more than one pulp and those excited from both pulp and extrapulpal soft tissue. Within each of these 3 pulp-driven subsets, some units responded to single shock, others only to a train of shocks. Mean discharge latency was shortest for the population excited only from soft tissue, intermediate for pulp-driven units excited by single shock and longest for pulp-driven units excited only by trains of shocks. Both soft tissue and pulp stimuli evoked extensive inhibitory effects. In the Discussion, the possible role of pulp-driven neurons in pain is considered. The functional properties of some neurons are consistent with a role in stimulus localization but those of the remaining neurons suggest other roles in pain. An examination of the literature on cortex and pain suggests that normally somatosensory cortex is important for localizing painful stimuli and that it contributes to other pain mechanisms as well. After certain lesions, somatosensory cortex has the capacity for generating "central" pain just like other structures in the nociceptive pathway.

Graphic digitizer analysis of the myelinated axon spectrum in the inferior alveolar nerve of the cat.

The diameter spectrum and other parameters indicating size and shape of myelinated axons were established in a cross-section of the inferior alveolar nerve obtained at the mandibular foramen. The spectrum is bimodal with approximately equal numbers of axons in the Aalpha and Adelta-range, in contrast to unimodal spectra of certain branches contributing to the inferior alveolar nerve.

Graphic-digitizer analysis of axon spectra in ethmoidal and lingual branches of the trigeminal nerve.

Sections were removed from the lingual and ethmoidal nerves of cats and histologically prepared, and the fibers were analyzed under the light microscope. Neural dimensions were measured by a new technique, employing a graphic digitizer and computer. The outline of a neural structure was traced with the digitizer pen, and the total number of axons, their cross-sectional areas, shapes, diameter spectra, and locations within the nerve were calculated. Both nerves had unimodal axon spectra with the peak between 2 and 6 mum diameter. Differences in axon composition occurred over the diameter range of 9 to 20 mum; the lingual nerve had many axons in this range, the ethmoidal nerve only a few. The total number of myelinated axons was near 4000 in the lingual nerve, near 1400 in the ethmoidal nerve; only the latter had many large-sized Remak bundles (containing C-fibers). Most myelinated axons were not perfectly circular but exhibited various degrees of distortion.