Composition of the medial and posterior articular nerves of the mouse knee joint

The number and the distribution of fiber size in the medial (MAN) and posterior (PAN) articular nerves of the mouse knee joint were studied by electron microscopy. The MAN contained 75 +/- 28 nerve fibers consisting of 63 +/- 24 unmyelinated and 12 +/- 6 myelinated fibers. The PAN was composed of 195 +/- 50 nerve fibers, namely 129 +/- 28 unmyelinated and 66 +/- 24 myelinated fibers. A skewed unimodal distribution of the unmyelinated nerve fiber diameters was seen in both nerves ranging from 0.1 to 1.2 microm with a maximum between 0.3 and 0.6 microm. The myelinated nerve fibers in the MAN ranged from 1 to 8 microm with a peak between 2 and 5 microm. In the PAN, their diameters ranged from 1 to 12 microm with a clearly visible peak at 4-5 microm and a plateau at 8-9 microm that may represent a second maximum. These data show that the knee joint innervation of the mouse is comparable to those of the cat and rat concerning the types of nerve fibers and the composition of the two nerves. However, in relation to the much smaller area of tissue to be innervated the total number of primary afferents is considerable smaller in the mouse.     

The morphological consequences of neonatal treatment with capsaicin on primary afferent neurones in adult rats

A comparison was made using our work and that reported in the literature of the losses of myelinated and unmyelinated fibres in a variety of nerves and also of losses of nerve cells in dorsal root ganglia, after treatment of neonatal rats with capsaicin. In L3 and L4 dorsal roots 85-93% of unmyelinated fibres and 9-33% of myelinated fibres were lost after 50-100 mg/kg capsaicin neonatally. In rats treated with 85 mg/kg capsaicin, percentage losses of unmyelinated (89%) and myelinated (36%) fibres of L4 dorsal roots were remarkably similar to the calculated losses of small dark (92%) and large light (34%) neurones respectively in these ganglia. Studies with monoclonal antibody RT97 which labels the large light neurones only, confirmed that some RT97 negative cells (i.e. small dark neurones) remain after capsaicin treatment. At present no evidence exists to suggest that the cell death of small dark neurones or C fibres after neonatal capsaicin treatment is completely selective for subgroups of these neurones, either in relation to sensory modality, or in relation to immunocytochemical cell markers and peptide content. However much more data is required to establish whether this cell death is really nonselective as regards immunocytochemical markers.     

The Fine Anatomy of the Optic Nerve of Anurans—An Electron Microscope Study

In the optic nerve of Anurans numerous myelinated and unmyelinated axons appear under the electron microscope as compact bundles that are closely bounded by one or several glial cells. In these bundles the unmyelinated fibers (0.15 to 0.6 µ in diameter) are many times more numerous than the myelinated fibers, and are separated from each other, from the bounding glial cells, or from adjacent myelin sheaths, by an extracellular gap that is 90 to 250 A wide. This intercellular space is continuous with the extracellular space in the periphery of the nerve through the numerous mesaxons and cell boundaries which reach the surface. Numerous desmosomes reinforce the attachments of adjacent glial membranes. The myelinated axons do not follow any preferential course and, like the unmyelinated ones, have a sinuous path, continuously shifting their relative position and passing from one bundle to another. At the nodes of Ranvier they behave entirely like unmyelinated axons in their relations to the surrounding cells. At the internodes they lie between the unmyelinated axons without showing an obvious myelogenic connection with the surrounding glial cells. In the absence of connective tissue separating individual myelinated fibers and with each glial cell simultaneously related to many axons, this myelogenic connection is highly distorted by other passing fibers and is very difficult to demonstrate. However, the mode of ending of the myelin layers at the nodes of Ranvier and the spiral disposition of the myelin layers indicate that myelination of these fibers occurs by a process similar to that of peripheral nerves. There are no incisures of Schmidt-Lantermann in the optic myelinated fibers.     

Degenerationsstudien am Nervus pinealis von Rana esculenta L. nach stirnorgannaher und -ferner Durchtrennung

Zusammenfassung Am Nervus pinealis von Rana esculenta wurde der Verlauf der Wallerschen Degeneration nach Durchtrennung des Nervenstrangs unterhalb des Stirnorgans studiert.30 Std nach der Läsion tritt im distalen Stumpf der markhaltigen Nervenfasern eine Anhäufung von Glykogen auf; granulär-vakuolige Veränderungen zeigen diese Faserabschnitte am 4. Tag. Veränderungen der Myelinscheide beginnen am 7. postoperativen Tag an den Innenlamellen und greifen dann auf die ganze Markscheide über. Die Desintegration der einzelnen markhaltigen Fasern eines Nervus pinealis verläuft verschieden schnell; nach 25 Tagen ist sie an den meisten Fasern abgeschlossen.Am 7. Tag sind die ersten Veränderungen an den marklosen Fasern zu beobachten. Dabei werden die peripher in der Hüllzelle liegenden Fasern durch Retraktion des Hüllzellzytoplasmas ins Interstitium ausgestoßen und gehen dort zugrunde. Die mehr zentral in den Hüllzellen lokalisierten Fasern bleiben hingegen vom Hüllplasma umgeben. Die Degeneration dieser marklosen Elemente ist nach 14 Tagen abgeschlossen; es resultiert ein mit homogenem Inhalt geringer Elektronendichte gefüllter Kanal, der auf Querschnittsbildern eine Vakuole vortäuscht.Weiterhin ist für den degenerierenden Nervus pinealis eine starke Fibrosierung sowie der Schwund der intra- und perineuralen Lymphspalten charakteristisch. Nach etwa 60 Tagen treten im distalen Nervenstumpf von Büngnerschen Bändern umgebene marklose Nervenfasern auf. Dieses Auswachsen von Nervenfasern bestätigt elektrophysiologische Ergebnisse von Morita (s. Dodt und Morita, 1967), daß im Nervus pinealis erregungsleitende Elemente in beide Richtungen ziehen (frontofugale und frontopetale Fasern).Bindegewebsstrukturen, Degenerationsablauf und Strukturbild der Hüllzellen lassen den Nervus pinealis als peripheren Nerven erscheinen.

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Degeneration pattern of the pineal nerve of rana esculenta after transection at different anatomical levels

Summary Wallerian degeneration was studied in the pineal nerve of Rana esculenta with the electron microscope after transection of the nerve beneath the frontal organ.30 hours after the operation an accumulation of glycogen was found in the distal stump of the myelinated axons. Four days after interruption these axons displayed signs of granular and vaculoar disintegration. Myelin sheath changes started at the seventh day after the operation at the level of the inner lamellae and were subsequently followed by changes in the outer lamellar systems. The velocity of disintegration varied for individual myelinated fibers. 25 days after transection of the pineal nerve most of its myelinated fibers were completely degenerated.Initial changes of the unmyelinated fibers were recognized at the seventh postoperative day. Fibers located peripherally in the satellite cell were exposed by retraction of the satellite cytoplasm and degenerated rapidly. On the other hand, unmyelinated fibers which were located more centrally remained within the satellite cell and completed their degeneration only after 14 days. The residual structure observed was a channel occupied by a homogeneous material of low electron density.The number of collagen fibers increased and the intra- and perineural lymph spaces were obliterated in the distal nerve stump. Approximately 60 days after the operation chains of satellite cells and unmyelinated nerve fibers reappeared in the distal nerve stump. This result confirms the electrophysiological data of Morita (cf. Dodt and Morita, 1967) that nerve fibers run in both directions within the pineal nerve (i.e. they are frontofugal and frontopetal with respect to the frontal organ).The properties of the connective tissue between the pineal nerve fibers, the pattern of degeneration and the fine structure of the satellite cells suggest that the pineal nerve of Rana esculenta has the structure of a peripheral nerve rather than that of a central nervous tract.

Mit Unterstützung durch die Deutsche Forschungsgemeinschaft. Ein Druckkostenzuschuß wurde aus Institutsmitteln zur Verfügung gestellt.     

Functional and ultrastructural changes in the midbrain tectum of the frog after enucleation

In experiments on frogs immobilized with Diplacin at different times after unilateral enucleation, as degeneration of the optic fibers and their terminals developed, a successive disappearance of the components of evoked potential (EP) was observed; this indicates the direct dependence of the rate of degeneration on the diameters of the fibers. The nature of the ultrastructural changes also depends on the diameter of the cut axons: the terminals of all or some of the myelinated fibers of large diameter degenerated with the condensation of the endings and of all the cytoplasmatic organelles ("dark" type); the terminals of thin myelinated and unmyelinated fibers degenerated with a gradual lysis of organelles ("light" type). Unmyelinated optic fibers and their synapses survived and transmitted the excitation for more than 140 days at a temperature of 18–20°C. In the course of the survival of optic fibers and synapses, the static (latency, duration, and amplitude) as well as dynamic (lability, excitability cycle, and posttetanic changes) characteristics of the EP for electrical stimulation of the nerve changed insignificantly. Direct response of the midbrain tectum decreased in the course of the degeneration of the optic fibers, and after 280 days its amplitude was about 20% of the control value.A. N. Severtsov Institute of Evolutionary Morphology and Ecology of Animals, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 2, No. 2, pp. 180–188, March–April, 1970.     

Morpho-functional changes in the turtle midbrain tectum after enucleation

Morpho-functional changes in the tectum mesencephali during degeneration after enucleation were studied inEmys orbicularis L. Comparison of amplitude-time characteristics of evoked potentials of the visual center with degenerative changes in axon terminals and fibers of the optic nerve in the same animals revealed a "light" type of degeneration of the terminals of unmyelinated axons and a "dark" type in terminals of myelinated axons. During "dark" degeneration (4–5 months after enucleation) the low-amplitude presynaptic component of the evoked potential, reflecting excitation of large myelinated fibers, disappeared and changes occurred in the characteristics of the first high-amplitude component, the appearance of which is connected with excitation of myelinated fibers of medium diameter. The last component disappeared 7 months after the operation, along with disappearance of the "dark" degeneration. During "light" degeneration (2.5–3.5 months) changes took place in the characteristics of the second high-amplitude component of the evoked potential, which reflects excitation of thin fibers, both myelinated and unmyelinated, whose ranges of diameters overlap. This component disappeared after 6–7 months, almost simultaneously with disappearance of the first high-amplitude component, as the result of simultaneous completion of degeneration of myelinated fibers of medium and small diameter.     

Acetylcholinesterase: a histochemical identification of motor and sensory fascicles in human peripheral nerve and its use during operation

To evaluate the precision of acetylcholinesterase histochemical identification of motor and sensory fascicles, this study presents a systematic observation of human peripheral nerves by Karnovsky and Roots' histochemical method. The results indicate that either of the enzymatic activities of myelinated and unmyelinated fibers was different between motor and sensory fascicles. Fifty-seven percent of the myelinated fibers showed enzymatic activity in the motor fascicles, while none of the myelinated fibers in the sensory fascicles showed enzymatic activity. The unmyelinated fibers showing enzymatic activity in the sensory fascicles were far denser than those in the motor fascicles. Our study demonstrated that the unmyelinated fibers were sympathetic postganglionic unmyelinated fibers. From these results it is concluded that the motor and sensory fascicles may be identified not only according to the enzymatic activities of the myelinated fibers, but also according to the enzymatic activities of the sympathetic postganglionic unmyelinated fibers. An improved histochemical method was suggested for its applicability as a method of intraoperative nerve fascicle identification. Simulated experiments were done on the radial nerves and the median nerves in human cadavers. This improved histochemical process can be completed within 50 minutes and can be used in intraoperative nerve fascicle identification.     

Quantitative studies on the intermediate nerve of the mouse with the electron microscope.

Quantitative counts of the intermediate nerve fibers of the mouse with electron microscope have shown that, on an average, 1,267 (79.3%) and 301 (18.9%) of the total nerve fibers (1,597) were myelinated and unmyelinated fibers, respectively. The number of unmyelinated fibers in the intermediate nerve was less than one-half the number of unmyelinated fibers in the greater petrosal nerve found in previous studies. Therefore, it is postulated that some of the unmyelinated fibers in the greater petrosal nerve may come from the intermediate nerve, while the rest may be derived from another source.     

Quantitative studies on the motor root of the mouse facial nerve. An electron-microscopic study.

Fiber count analysis was performed with the electron microscope on the motor root of the facial nerve in six mice. On an average, 3,433 (84.9%) of the total nerve fibers (4,046) were myelinated and 592 (14.6%) unmyelinated. The motor root consisted mostly of large myelinated fibers (large fiber group), but a part of the root consisted of small myelinated and unmyelinated fibers (small fiber group). The nerve fibers of the small fiber group appear to correspond with those of the intermediate nerve, and to pass through the motor root and enter the intermediate nerve near the geniculate ganglion.     

A quantitative electron microscope analysis of peripheral nerve in the urodele amphibian in relation to limb regenerative capacity

An approximate 1:1 ratio of myelinated to unmyelinated fibers was established in counts from electron micrograph montages in nerves of the newt, Triturus (Notophthalmus) viridescens. The number of myelinated fibers correspond to the number counted with the light microscope after osmium fixation. Light microscope counts of silver impregnated sections yielded a value slightly higher suggesting that, except for bundles of unmyelinated fibers, the silver technique revealed mainly myelinated fibers. The results were used to reassess previous quantitative studies on the relation between number of nerve fibers and the control which nerves exert on regeneration. For a truer estimate of the number of axons affecting regeneration, fiber values previously reported should now be doubled to include the large number of unmyelinated fibers. However, calculations show that the unmyelinated fibers contribute less than 3% of the total neuroplasm in the peripheral nerve. Finally, counts made of Schwann cells and fibroblasts show that the latter are few in number.     

Excitation of cat spinal cord dorsal column fibers during stimulation of different fiber groups of cutaneous and somatic nerves

The effects of electrically stimulating different groups of nerve fibers supplying the skin and muscle on evoked potentials in cat spinal cord dorsal columns were studied. Significant differences in the configuration of dorsal column potentials recorded in response to stimulation of these nerves were found. It was shown that cutaneous nerve unmyelinated fibres were connected to unmyelinated dorsal column fibers. In addition, excitation of cutaneous C-fibers lead to activation of dorsal column fibers with the maximum conduction velocity. The somatic nerve was only connected to myelinated dorsal column fibers, and excitation of its non-myelinated fibers did not cause other types of dorsal column fibers to be activated. It is suggested that the acceleration of cutaneous signal transmission in the dorsal column system may be brought about by the necessity for rapid warning of potentially harmful stimuli.Medical Institute, Russian Federation Ministry of Public Health, Nizhny Novgorod. Translated from Neirofiziologiya, Vol. 24, No. 5, pp. 625–635, September–October, 1992.     

Adenosine triphosphatase activity of cutaneous nerve fibers

Summary The histochemical study of Mg⁺⁺-activated adenosine triphosphatase (Mg⁺⁺-ATPase) activity was carried out on the peripheral nerves of mouse digital skin by light and electron microscopy. Under the light microscope, the ATPase activity was clearly demonstrated on the nerve fibers as a fine network in the subepidermal regions. Under the electron microscope, the reaction product of enzyme activity was located in the interspace between axolemma and the surrounding Schwann cells of the unmyelinated nerve fibers. No reaction product was observed in the space between the axolemma and the Schwann cells associated with myelinated nerve fibers. Demonstrable activity was absent at the nodes of Ranvier as well as on the para- and internodal regions of these myelinated axons. The part of the axolemma lacking a Schwann cell sheath failed to show a reaction product. The perineural epithelial cells surrounding the nerve fibers displayed reaction product in the caveolae. These results suggest a functional difference in the axon-Schwann interface of myelinated as compared to unmyelinated nerve fibers. The function of the perineural epithelial cell would be expected to be a regulatory one in transferring materials across the epithelium to keep the proper humoral environment around nerve fibers.     

Axonal degeneration of peripheral facial nerve in a patient with progressive hemifacial atrophy.

We report a case of a 23-year-old woman with progressive hemifacial atrophy. She showed an atrophic change on the left side of her face for 8 years. A skin biopsy obtained from the lesion revealed the fibrotic changes in the deep dermis and adipose tissue with infiltrations of lymphocytes and plasma cells. She underwent the augmentation using a deepithelialized anteromedial thigh flap with endoscopic assistance. A specimen of the peripheral facial nerve taken from the region adjacent to the skin lesion during the operation showed atrophy of neurofibers with vacuole degeneration. On an electron microscopic examination, a high degree of degeneration of myelinated and unmyelinated axons was observed. These findings may provide direct evidence that atrophic changes of nerve fibers are closely related with the pathology of this disease.     

Composition of the medial and posterior articular nerves of the mouse knee joint

The number and the distribution of fiber size in the medial (MAN) and posterior (PAN) articular nerves of the mouse knee joint were studied by electron microscopy. The MAN contained 75 &#45 28 nerve fibers consisting of 63 &#45 24 unmyelinated and 12 &#45 6 myelinated fibers. The PAN was composed of 195 &#45 50 nerve fibers, namely 129 &#45 28 unmyelinated and 66 &#45 24 myelinated fibers. A skewed unimodal distribution of the unmyelinated nerve fiber diameters was seen in both nerves ranging from 0.1 to 1.2 &#119 m with a maximum between 0.3 and 0.6 &#119 m. The myelinated nerve fibers in the MAN ranged from 1 to 8 &#119 m with a peak between 2 and 5 &#119 m. In the PAN, their diameters ranged from 1 to 12 &#119 m with a clearly visible peak at 4-5 &#119 m and a plateau at 8-9 &#119 m that may represent a second maximum. These data show that the knee joint innervation of the mouse is comparable to those of the cat and rat concerning the types of nerve fibers and the composition of the two nerves. However, in relation to the much smaller area of tissue to be innervated the total number of primary afferents is considerable smaller in the mouse.     

Acetylcholinesterase activity of motor and sensory nerve fibers in the spinal nerve roots of the rat

Summary The histochemical and cytochemical distribution of acetylcholinesterase activity in the anterior and posterior spinal nerve roots and ganglia of the rat was demonstrated by the Karnovsky method using acetyl and butyrylthiocholine as substrates and eserine and DFP as inhibitors. Light and electron microscopic examination of transverse frozen sections enabled the simultaneous visualization of end product in relationship to the various fiber components of each nerve root. While the enzymatic activity of the anterior roots was consistantly observed in the large extrafusal and small intrafusal motor fibers a relatively greater amount of precipitate occurred in aggregates of myelinated and unmyelinated fibers believed to represent preganglionic sympathetic nerves. In contrast, no significant enzymatic activity could be demonstrated in the myelinated nerve fibers of the posterior root. In the sensory sytem, the limited enzymatic precipitate was largely restricted to the unmyelinated afferent fibers and to their small cell bodies in the dorsal root ganglia. The ultrastructural distribution of enzymatic activity was located in the granular endoplasmic reticulum and perinuclear spaces of the ganglion cells. Within peripheral nerves this end product occurred between the apposing axonal and Schwann cell membranes and along the membranous aspect of occasional axoplasmic vesicles of both myelinated and unmyelinated nerve fibers.This study was supported by grants NB 04161-04 and NB 04161-05 of the National Institute of Neurological Diseases and Blindness. — The author would like to thank MissMaria C. la Valle for her skillful technical assistance.     

扬子鳄视神经的研究

本文研究了扬子鳄的视神经。结果明明,视神经中可见有髓纤维和无髓纤维。有髓纤维分布均匀,无髓纤维常聚集成团;胶质细胞核,在视神经中可看到两种类型,有髓纤维总数为２００,０００－３００,０００根,纤维直径范围为０．４１－６．６６μｍ,只有一个峰值,峰直径为１．３１μｍ;纤维轴突径与纤维直径之比（ｄ／Ｄ）约为０．７３－０．７５。经统计分析,同个体左右侧神经纤维数目有差异,同一神经中周围区与中央区数目分布     

Light and electron microscopic studies on the pineal tract of rainbow trout, Salmo gairdneri.

The pineal tract of rainbow trout from the pineal end vesicle to the posterior commissure was studied by light and electron microscopy. Five types of nerve fibres (photoreceptor basal process, ganglion cell dendrite, electron-lucent fibre and synaptic vesicles, myelinated and unmyelinated axons) and two modes of synapses (photoreceptor basal process ganglion cell dendrite and axon terminal with synaptic vesicles-photoreceptor basal process synapses) are distinguishable in the proximal region of end vesicle. The two distinct synaptic associations with the photoreceptor basal process suggest two different (excitatory and inhibitory) control of pineal sensory activity. At the distal portion of stalk about two thousand nerve fibres converge into dorsal and ventral bundles. Posterior to the habenular commissure several small branches run out laterally from the ventral bundles to the basal margin of the ependyma, but not into the habenular commissure. The dorsal bundle passes through the dorsal side of the subcommissural organ and runs ventral to the posterior commissure. The pineal tract is composed of unmyelinated axons, electron-lucent nerve fibres and myelinated axons. The number of fibres increases throughout the stalk and reaches the maximum number at the opening of pineal lumen to IIIrd ventricle, however, the number of fibres then decreases through the subcommissural organ and posterior commissure. This increase and decrease of nerve fibres suggest the continuous participation of axonal fibres of pineal nerve cells and the ramification or branching of pineal tract, respectively.     

Electron-microscopic analysis of the mouse facial nerve near the geniculate ganglion

An electron-microscopic analysis of the mouse facial nerve near the geniculate ganglion shows that there are, on the everage, 603 more nerve fibers in the portion of the nerve distal to the geniculate ganglion than there are in the part proximal to the ganglion. The average distal increase in the number of unmyelinated fibers is 444 and that in the myelinated fibers is 165. The somatic motor nerve fibers and the parasympathetic fibers in the mouse facial nerve may not contribute to the distal excess. It is possible that the increase in the number of unmyelinated fibers distal to the geniculate ganglion is mainly due to the presence of postganglionic sympathetic fibers in the facial trunk distal to the geniculate ganglion and the greater petrosal nerve. The distal increase in the number of myelinated fibers may be mainly contributed by the sensory fibers.     

Acetylcholinesterase activity in nerve endings of tails of Rana japonica and R. catesbeiana during metamorphosis

Summary In anuran tadpole tails, the myelinated motor nerve fibers branch in the myoseptum to innervate both red and white muscle fibers at, or near, their ends. There are no significant ultrastructural differences between the nerve endings of the two types of muscle fibers.Intense acetylcholinesterase reaction product was observed in synaptic clefts and junctional folds, as well as in transverse tubules. As metamorphosis proceeded, the junctional folds of the nerve endings disappeared, however, acetylcholinesterase reaction product was still observed in the synaptic clefts. As muscle fibers began to degenerate, nerve endings began to separate from them. However, after nerve endings were completely separated from the surfaces, degenerated muscle fibers, synaptic and cored vesicles were still well preserved although no acetylcholinesterase reaction product was found. It seems clear that the mechanism of the muscle degeneration in the tadpole tail during metamorphosis is not the result of the degeneration of its nerve endings.     

Localization of Phospholipid Synthesis to Schwann Cells and Axons

Quantitative electron microscopic autoradiography was used to detect and characterize endoneurial sites of lipid synthesis in mouse sciatic nerve. Six tritiated phospholipid precursors (choline, serine, methionine, inositol, glycerol, and ethanolamine) and a protein precursor (proline) were individually injected into exposed nerves and after 2 h the mice were perfused with buffered aldehyde. The labeled segments of nerve were prepared for autoradiography with procedures that selectively remove nonincorporated precursors and other aqueous metabolites, while preserving nerve lipids (and proteins). At both the light and electron microscope levels, the major site of phospholipid and protein synthesis was the crescent-shaped perinuclear cytoplasm of myelinating Schwann cells. Other internodal Schwann cell cytoplasm, including that in surface channels, Schmidt-Lanterman incisures, and paranodal regions, was less well labeled than the perinuclear region. Newly formed proteins were selectively located in the Schwann cell nucleus. Lipid and protein formation was also detected in unmyelinated fiber bundles and in endoneurial and perineurial cells. Tritiated inositol was selectively incorporated into phospholipids in both myelinated axons and unmyelinated fibers. Like inositol, glycerol incorporation appeared particularly active in unmyelinated fibers. Quantitative autoradiographic analyses substantiated the following points: myelinating Schwann cells dominate phospholipid and protein synthesis, myelinated axons selectively incorporate tritiated inositol, phospholipid precursors label myelin sheaths and myelinated axons better than proline.