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The ultrastructure of the sensory nerve endings in the articular capsule of the knee joint of the domestic cat (Ruffini corpuscles and Pacinian corpuscles).

Two types of mechanoreceptor have been found in the articular capsule of the knee joint of the domestic cat--Ruffini corpuscles and Pacinian corpuscles. Ruffini corpuscles are situated in the stratum fibrosum and consist of 2 to 6 cylinders. Each cylinder is made up of an afferent axon (diameter 3-4 micrometer), its swellings and terminal processes, Schwann cells enveloping the nerve swellings and terminal processes, endoneural connective tissue and a perineural capsule. The perineural capsule is incomplete in Ruffini corpuscles. The Pacinian corpuscles are 20 to 40 micrometer wide and 150-250 micrometer long. They are situated in groups of up to five at the boundary between the stratum synoviale and the stratum fibrosum. The afferent axon is myelinated (diameter 3-5 micrometer). Its terminal portion is inside the inner bulb which is formed of modified Schwann cells. Each corpuscle is enveloped by a perineural capsule (4-8 layers). The ultrastructure of the Pacinian corpuscles is compared with the ultrastructure of the skin receptors in the cat.

Animals

Role of extracellular matrix in the regeneration of a pacinian corpuscle.

The pacinian corpuscle is composed of an inner and an outer core or bulb. The former is formed by tightly packed and multi-layered thin cellular processes (lamellae) of lamellar cells which surround a centrally located axon terminal, and the latter, also called the capsule, is made up of very loosely piled layers of thin cells which encircle the inner core. Lamellar cells of the inner core are considered to be specialized Schwann cells, and the outer core cells are modified perineurial cells. In the present study, the matrix filling the extracellular spaces of the inner core consisted of basal lamina-like amorphous materials, sparce fine collagen fibrils, and the ground substance embedding these structural components. No definite basal laminae were found on the inner core lamellae except on the peripherally located ones which had distinct basal laminae. Outer-core cells were invested along the entire contour by distinct basal laminae. The interspace between the inner and outer cores was a continuation of the nerve endoneurium. The purpose of this investigation was to determine whether the extracellular matrix of the pacinian corpuscle, especially that of the inner core, has the ability to cause corpuscle regeneration, i.e. to make the regenerating axons and Schwann cells differentiate into corpuscular axon terminals and inner core cells, respectively. Pacinian corpuscles in the periosteum at the distal end of the fibula of mice were repeatedly frozen (3-5 times) in situ with forceps cooled with liquid nitrogen. Within 2-3 days, all the cellular constituents of the corpuscle had degraded, while the extracellular matrices of the inner and outer cores apparently remained undamaged. After 5-7 days, regenerating axons and accompanying immature Schwann cells entered these extracellular matrices of the inner cores. A remarkable finding was that these immature Schwann cells were detached from the axon, and sent thin cellular processes around the axon in a characteristic fashion, basically forming the same pattern as lamellae in a normal corpuscle. The regeneration of the inner core was completed by about 40 days after the freezing treatment. In the outer core, perineurial cells proliferated and extended through the basal lamina tubes of the old cells, becoming new outer core cells. These findings indicate that the extracellular matrix of the pacinian corpuscle has a specific property to cause the regeneration of the corpuscle.

Animals

Depolarizing and hyperpolarizing receptor potentials in the non-myelinated nerve terminal in pacinian corpuscles.

1. Pacinian corpuscles or non-myelinated nerve terminals in Pacinian corpuscles, from which lamellae had been removed, were stimulated with linearly increasing compression of varying rate, which decayed linearly after a maximum compression.2. An impulse was initiated with a compression having a rate of increase greater than a critical slope. The critical slope was 1.1-1.2 rheobase/msec in both intact corpuscles and decapsulated terminals.3. The receptor potential of the terminal increased in magnitude and rate of rise with an increase in the rate of compression. Its rate of rise was linearly related to the rate of compression.4. Hyperpolarization was observed on removal of compression, and an impulse was initiated upon recovery of the hyperpolarized membrane potential.5. In some corpuscles or decapsulated terminals hyperpolarization was produced on compression and a depolarizing response was produced upon removal of compression. After rotation by 90 degrees along their long axis, they produced depolarization on compression.6. Difference in the directional sensitivity of corpuscles and decapsulated terminals was confirmed and was explained on the basis of the shape of the terminal.7. On- and off-responses of variable latency recorded from a central portion of the axon to Pacinian corpuscles were explained by the depolarizing and hyperpolarizing responses in the terminal.

Animals

[Oscillation of impulse discharges of Pacinian corpuscles of cat mesentery to external stimulation].

A sensory unit with one or two Pacinian corpuscles was isolated from cat mesentery and square wave mechanical stimulation (duration 5-10 sec), sinusoidal frequency stimulation (duration 4-130 sec, frequency 0.06-300 Hz) and ramp mechanical stimulation (duration 5-10 sec) were applied to the Pacinian corpuscles. When the temperature exceeded 27 degrees C, the sensory unit caused a sustained discharge after on-response to the square wave stimulation. The sustained discharge lasted until the off-response. The sustained discharge was considered to be generated by an oscillation of the receptor potential in the Pacinian corpuscles. The results were as follows: 1. Sensory units with two Pacini corpuscles of cats from young (20 days after birth) to adult were found to respond with both fast-adapting and apparent slow-adapting responses at room temperature (27 degrees C). 2. The two Pacini corpuscles showed the characteristics of fast-adapting mechanoreceptor and vibrator. It was confirmed that the apparent slow-adapting responses from the sensory units were not artifacts induced by vibration from the stimulating bar or experimental table or experimental room, but were originated by an unknown mechanism in the corpuscles. 3. Some sensory units with two Pacinian corpuscles also responded with both fast-adapting and apparent slow-adapting responses in the range of 27-29 degrees C. The apparent slow-adapting responses were caused by pressure and vibratory stimulations above a strength level, but not by dumping of the stimulating bar. 4. The sensory unit evoked only the fast-adapting discharges near the threshold level of stimulus strength at less than 27 degrees C. In the temperature range of 27-40 degrees C, the sensory unit showed an increase in frequency of the apparent slow-adapting discharge by increased displacement and velocity of the stimulus. 5. The sensory unit responded with repeated firing to low-frequency stimulation (0.1-0.06 Hz) at the temperature range and the impulse number was increased by increased strength of the low-frequency stimulation. 6. At the 27-40 degrees C, the sensory units with Pacinian corpuscles evoked after discharge and spontaneous discharges and the impulse number was increased by increased displacement, velocity and frequency of the mechanical stimulus. Thus it is difficult to call the response of Pacinian corpuscles observed at more than 27 degrees C a slow-adapting one, judging from the duration of the receptor potential. We considered that these discharge responses resulted from an electrical oscillation of the receptor potential in the corpuscles.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals

[The effect of cholinergic substances on individual mechanoreceptors--Pacinian corpuscles].

Acetylcholine and nicotine application to the intact pacinian corpuscle failed to stimulate the spike activity, but changed the sensitivity to the mechanical stimulation: low concentration (1.10(-6) g/ml) increased the sensitivity and high concentration (1.10(-4) g/ml) decreased it. This influence can be attributed to the action of these substances on the structures which generate the action potentials. Acetylcholine application to decapsulated pacinian corpuscles stimulated the appearance of the spike activity. This reaction was possibly connected with the acetylcholine influence on the mechanoreceptive zones proper. Tubocurarine or hexonium application of decapsulated pacinian corpuscles led to depression of the sensitivity of the receptor to the mechanical stimulation that can also be explained by the participation of acetylcholine in the process of adequate receptor stimulation.

Acetylcholine

Pacinian corpuscle hyperplasia in the hand.

Proliferation of pacinian corpuscles adjacent to the digital nerves in the hand is very rare. Patients are usually seen initially with a history of previous trauma and severe localized pain. The symptoms, signs, and surgical treatment of previously reported cases are reviewed and histological criteria from this case are proposed to define this condition. In addition to a neuroma or glomus tumor, pacinian corpuscle hyperplasia should be considered in the differential diagnosis of digital or palmar pain.

Diagnosis, Differential

Pacinian corpuscle neuroma of digital nerves.

Symptoms and incapacitation due to abnormal aggregations of pacinian corpuscles are uncommon. Indeed, only three reports have been found in the scientific literature. A case is presented in which the patient's chief complaint was pain and localized tenderness in the hand which interfered with normal activity. Surgical exploration of the palm showed abnormalities of pacinian corpuscles attached to the median digital nerve in the form of a grape-like cluster and a single enlarged corpuscle beneath the epineurium; the abnormality attached to the ulnar digital nerve appeared as an offshoot of hyperplastic corpuscles lying in tandem. The abnormal corpuscles were excised. The symptoms have not recurred to date. These abnormalities in size, position, and number of pacinian corpuscles are compared to the findings of the few other reports in the literature. The neuroma formation found attached to this ulnar nerve has not been cited previously.

Adult

Macrophages in Pacinian corpuscles.

The presence of macrophages in the outer bulb region of mouse, monkey and human Pacinian corpuscles was demonstrated by light and electron microscopy. In the normal, nontreated, Pacinian corpuscles, a few particular cells were located in the spaces between lamellae of the outer bulb. These cells contained numerous vesicles and vacuoles, and various cytoplasmic processes. When horseradish peroxidase (HRP) was injected locally or systemically, many HRP-positive cells, which were considered to be similar to the particular cells described above, were found in the outer bulb region of the corpuscles. Electron microscopy revealed that these cells contained HRP in vesicles and vacuoles, suggesting that they were macrophages vigorously taking up exogenous HRP. Macrophages in the Pacinian corpuscles are considered to work as scavengers to keep the inner environment of the corpuscles clear and constant with regard to its macromolecular content.

Animals

The cytology of human Pacinian corpuscles: evidence for sprouting of the central axon.

During the course of the studies on non-traumatized Pacinian corpuscles from normal human adults, we have frequently encountered corpuscles which have an 'apparently multiple' innervation in both light and electron microscopic preparations. On closer inspection of serial sections for both light and electron microscopy, these 'apparently multiple' axon terminals have been found in fact to be branches of the main central axon within the inner core of the corpuscle. Sprouting occurred at the trunk or at the extreme tip of the main axon, and such sprouts extended in various directions from the central axon throughout the inner core, producing tortuous and complex patterns of this 'multiple' innervation. These axonal sprouts do not have separate inner cores separated from one another, but rather are embedded in a common inner core. The presence of a common inner core thus differentiates normal axonal sprouts from the experimentally or pathologically produced multiple innervation that results form regeneration of axons in a previously denervated corpuscle. We conclude that the inner core of Pacinian corpuscles is a unique micro-environment promoting sprouting of sensory axon in the normal human adult as well as juvenile Pacinian corpuscles.

Adolescent

Reinnervation of transplanted pacinian corpuscles by ventral root axons: ultrastructure of the regenerated nerve terminals.

This study addresses two questions. Can mature, denervated and transplanted Pacinian corpuscles accept innervation from motor axons? If so, does the alien target influence the structural characteristics of the regenerated motor axon terminals? Pacinian corpuscles from the hind leg of young rats, together with a segment of the nerve branch through which they receive their sensory innervation, were autotransplanted to the surface of the spinal cord and the nerve stump anastomosed to the central stump of a transected lumbar ventral root. Between 4 and 5 months later the grafts were studied by electron microscopy. Ventral root axons regenerated through the endoneurial tubes of the grafted nerve to reach the corpuscles, most of which became reinnervated by one to three myelinated fibres. The fibres lost their myelin sheaths before entering the inner core, branched, and gave rise to multiple terminals in the inner core. The regenerated terminals were packed with spherical synaptic vesicles and closely resembled normal motor nerve terminals. Thus motor axons are able to reinnervate Pacinian corpuscles but the structural characteristics of the terminals are apparently not modified by the alien target tissue. This finding contrasts with previous studies, in which it was found that terminals of the central axons of large dorsal root ganglion cells, induced to reinnervate Pacinian corpuscles, displayed the structural characteristics of peripheral sensory endings rather than those of dorsal root terminals in the spinal cord.

Animals

Slow-adapting responses of the Pacinian corpuscles of cat planta.

Slow-adapting impulses were recorded from the single nerve fiber innervating the Pacinian corpuscle of the cat planta, which was stimulated by constant pressure. Slow-adapting Pacinian corpuscles responded to both low-frequency (0.1-0.01 Hz) and high-frequency (400-800 Hz) vibrations. Simultaneously performed electron microscopy showed that there were no definite ultrastructural differences between slow- and fast-adapting Pacinian corpuscles.

Adaptation, Physiological

The enigma of sensitivity in Pacinian corpuscles: a critical review and hypothesis of mechano-electric transduction.

The present report reviews the physiological and morphological specializations of Pacinian corpuscles and other mechanoreceptors that are present in the skin and connective tissues of the body as well as the cochlea. The remarkable sensitivity of Pacinian corpuscles is such that the only form of mechanical energy that could be perceived by a Pacinian corpuscle is a sound wave. In fact the human finger as demonstrated by Munger and Ide (1987) can perceive sound waves when water is the coupling agent. The structural specializations are equally remarkable with extensive membrane specializations of both the inner core and inner portion of the outer core. The halves of the inner core are each coupled with gap junctions and the inner portion of the outer core joined with numerous tight junctions. The cleft regions have specializations involving the axolemma that consist of numerous axonal spines containing bundles of filaments projecting into the cleft of the inner core. These structural specializations are thought to represent specializations for mechano-electric transduction analogous in many respects to the hair cells of the cochlea. A hypothesis for mechano-electric transduction is presented that may account in part for the extreme sensitivity of Pacinian corpuscles and other mechanoreceptors.

Animals

K and Na ion content in the Pacinian corpuscle fluid and its role in the activity of receptors.

1. Potassium and sodium concentrations within the Pacinian corpuscle fluid have been investigated in adult cats. The sodium and potassium contents of samples were estimated by means of integrative ultramicroflame photometry. 2. The analytical results showed the values of the potassium concentration in the Pacinian corpuscle fluid and in the blood plasma to be 6.19 +/- 0.72 and 2.78 +/- 0.38 mequiv/1, respectively. 3. The increasing excitability of the Pacinian corpuscle in potassium-rich solution was shown by electrophysiologic methods. In potassium-free solution two phases of changing receptor excitability were observed. 4. Removal of sodium from external solution reduced the receptor potential to 10% of its original value. 5. Some mechanisms of the increase in excitability of primary tissue mechanoreceptors and secondary mechanoreceptors of the sense organs are discussed.

Animals

A re-evaluation of the cytology of cat Pacinian corpuscles II. The extreme tip of the axon.

The present report is the second of two studies re-evaluating the cytological characteristics of Pacinian corpuscles. The extreme tip of the axon of a Pacinian corpuscle has been identified and is quite different from the previously described ultraterminal region. The latter is the site where the inner core lamellae begin to terminate and is characterized by a smooth axolemma. The extreme tip lacks inner core lamellae directly abutting the axolemma and is instead characterized by the presence of many axonal spines projecting into a matrix of basal lamina-like material. The extreme tip of the axon thus resembles the organization of the axolemma facing the clefts of the inner core. The axonal spines at the cleft and extreme tip are proposed as a site of restricted current flow due to the tight apposition of inner core lamellae to the axolemma of X-axis. The hemi-inner cores thus could restrict current flow to the cleft. These anatomical specializations could represent both a source and a sink for K+ ions during mechano-electric transduction and account in part for the exquisite sensitivity of Pacinian corpuscles to complex pressure waves.

Animals

The form and distribution of the receptive fields of Pacinian corpuscles found in and around the cat's large foot pad.

1. Firing thresholds of Pacinian corpuscles situated within or close to the large pad of the cat's hind foot have been determined following step displacements applied to various points on the pad surface.2. The most sensitive positions on the receptive fields of thirty-one corpuscles were distributed unevenly over the pad. About half were situated close to the interlobular crease lines, and most of the others were at the edge of the pad.3. Threshold receptive fields were usually of complex form, with more than one region of low threshold.4. The approximate locations of a number of Pacinian corpuscles whose fields had been mapped were determined by dissection.5. The most sensitive position on the pad was usually at the closest point to the corpuscle. If the corpuscle was situated outside the pad itself, it was therefore usually most easily excited from some point at the edge of the pad. However, a minority of Pacinian corpuscles were most easily stimulated from some region other than that closest to them.6. It is suggested that previous estimates of the ability of this population of receptors to transmit information about the positions of stimuli (Gray, 1966) must be re-evaluated in the light of the non-uniform distribution and asymmetry of their cutaneous receptive fields.

Action Potentials

Changes in primate Pacinian corpuscles following volar pad excision and skin grafting. A preliminary report.

Human fingertip avulsion injuries were simulated by excising volar digital pads in stump-tailed monkeys. Half the defects were covered with split-skin grafts from the forearm, and half with full-thickness grafts of fingertip skin. Innervated pacinian corpuscles were found in the center of these grafts 3 months after the operation. The site of origin of these corpuscles is undefined. Denervation and devascularization of pacinian corpuscles resulted in alterations of their gross architecture, size, and innervation. The possibility exists that these alterations result from a dynamic adaptation of pacinian corpuscles to environmental stress.

Animals

Role of the sympathetic innervation of the pacinian corpuscle.

An investigation was made into the nature of the role played by the noradrenergic innervation of the pacinian corpuscle. Corpuscles of the cat mesentery and mesocolon were used in all experiments. Blockade of noradrenergic beta receptors by dichloroisoproterenol and interference with norepinephrine release by reserpine are each capable of reversibly blocking mechanoelectric transduction by the pacinian corpuscle. The monoamine oxidase inhibitors iproniazid and phenelzine are capable of protecting the transducer from the blocking effects of reserpine. It is concluded that the presence of norepinephrine, as maintained by sympathetic tonus, is required for the afferent nerve terminal of the pacinian corpuscle to be mechanosensitive.

Animals

Specializations of plasma membranes in Pacinian corpuscles: implications for mechano-electric transduction.

Pacinian corpuscles of cat mesentery were studied with freeze-fracture and thin sectioning methods after chemical fixation. Intramembranous particles (IMPs) exhibit differences in both density and pattern of distribution between the axolemma of the smooth short axis (x-axis) region and that of the axonal spine region of the long axis (y-axis) of the axon terminal. The axolemma of the x-axis has IMPs at a density of 2687 +/- 581 per micron2 (mean +/- S.E.M.), and these particles are 9.0 +/- 1.7 nm (mean +/- S.D.) in diameter. In contrast, the axolemma of the y-axis has a higher density of IMPs (3607 +/- 612 per micron2) which are larger (diameter, 10.0 +/- 1.7 nm). The particle distribution is not homogeneous in x-axis membranes as there are small patchy areas devoid of particles scattered throughout the entire surface. The E-face of the axolemma has a low density of IMPs (approximately 200 per micron2 in both x- and y-axes). However, IMPs in the E-face are smaller (approximately 9 nm) in the x-axis than in the y-axis (approximately 10 nm). The inner core lamellar cells have IMPs at a density of 3276 +/- 739 per micron2 and 553 +/- 169 per micron2 in the P- and E-faces, respectively. The particles are about 10 nm in diameter in both faces. Many gap junctions occur between lamellar cells especially near the clefts, suggesting that hemilamellae of each inner core half are kept at the same electrotonic potential. The outer core lamellar cells have IMPs at a density of 2239 +/- 403 per micron2 and 536 +/- 123 per micron2 in their P- and E-faces, respectively. The particles are approximately 10 nm in diameter in both faces. A noteworthy finding is that tight junctions are prominent at cell-to-cell appositions within individual lamellae, especially in the first and second (or sometimes third) innermost lamellae of the outer core. These tight junctions are considered to be a barrier to the leakage of fluid and/or ions between interlamellar spaces as well as between inner and outer cores. An intermediate cell layer is identified between the inner and outer cores. The connective tissue space of this cell layer corresponds to the endoneurium, indicating that intermediate layer cells are comparable to endoneurial fibroblasts.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals