Ultrastructure of glycogen-membrane complexes in sensory nerve fibres of cat muscle spindles

1971 ◽  
Vol 121 (2) ◽  
pp. 199-217 ◽  
Author(s):  
N. Corvaja ◽  
P. C. Magherini ◽  
O. Pompeiano
Development ◽  
1961 ◽  
Vol 9 (3) ◽  
pp. 456-467
Author(s):  
P. Hník ◽  
J. Zelená

In young rats, following lesions of a peripheral nerve at birth, immature muscle spindles disintegrate during a short transition period (Zelená, 1957), and even after several months of reinnervation the reinnervated muscles are usually found to contain no spindles (Zelená & Hník, 1960). Nevertheless, occasional small spindles of atypical structure are observed in some of these muscles. In the present report, the structure and morphological characteristics of these atypical spindles were studied and compared with normal spindles. Since differences in fast and slow muscles may include differences in muscle receptors (Voss, 1937; Maruseva, 1947; Hagbarth & Wohlfahrt, 1952; Freimann, 1953; Cooper, 1960), the number, size, and distribution of spindles were studied in two muscles representing the two functional groups. The origin of atypical spindles in the reinnervated muscles is not clear. These spindles could either differentiate anew under the influence of regenerating sensory nerve fibres, or they could originate from spindles reinnervated before their ultimate disintegration had taken place.


1. The structure and innervation of muscle spindles from normal, de-afferented and de-efferented muscles of the cat hind limb were studied. The spindles were either completely isolated by microdissection, or were serially sectioned transversely. 2. All spindles contain two distinct types of intrafusal muscle fibre, ‘nuclear bag fibres’ and ‘nuclear chain fibres’, which differ in structure and innervation. 3. Nuclear bag muscle fibres, usually two per spindle, are less than half the diameter of extrafusal fibres, and each contains numerous large nuclei packed together in the equatorial region of the spindle. Nuclear bag fibres practically never branch. The fibres contain numerous myofibrils uniformly distributed in cross-sections, and relatively little sarcoplasm; they atrophy very slowly after the ventral spinal roots are cut. Several small motor nerve fibres (y, fibres) enter each spindle and terminate in a number of discrete motor end-plates on the nuclear bag muscle fibres. These y x end-plates lie in a group at each spindle pole and long lengths of nuclear bag fibre are free of motor innervation. 4. Nuclear chain muscle fibres, usually four per spindle, are about half the length and diameter of nuclear bag fibres in spindles in the leg muscles. The nuclear chain fibres in spindles from the small muscles of the foot may, however, equal the nuclear bag fibres in length, and in diameter beyond the ends of the lymph space. Each nuclear chain fibre contains a single row of central nuclei in the equatorial region; the fibres occasionally branch, but often none of them do so. They contain fewer myofibrils per unit area, irregular in size and distribution, and relatively more sarcoplasm, than nuclear bag fibres. Nuclear chain fibres atrophy nearly as rapidly as extrafusal fibres after the ventral roots are cut. A number of very fine motor nerve fibres fibres) enter each spindle and terminate in a network of fine axons and small nerve endings (the network’) situated on the nuclear chain muscle fibres in most regions other than the nuclear region. 5. All spindles receive both y 1 xand y 2 innervation, fibres forming slightly more than half of the total number of motor fibres which varies from seven in simple spindles in phasic muscles to twenty-five in the most complex spindles in tonic muscles. Both y 1 and y 2 fibres remain intact after dorsal root transection and degenerate following ventral root transection. The histological evidence supports the view that the yj and y2 nerve fibres at the spindles are derived from two types of stem fibre, neither of which belongs to the a group. 6. Each spindle has one primary sensory nerve ending, supplied by one group 1 a afferent nerve fibre, and from zero to five secondary sensory nerve endings, each supplied by one group II afferent nerve fibre. The primary sensory terminations lie on both nuclear bag and nuclear chain muscle fibres. The secondary sensory terminations lie predominantly on the nuclear chain muscle fibres. In spindles with several secondary sensory endings, their terminations may lie on the same region of nuclear chain fibres as motor endings of the y 2 network. 7. In general, spindles in tonic muscles have more secondary sensory endings and motor nerve fibres and endings than those in other muscles. Nuclear chain intrafusal fibres are probably functionally ‘slower’ than nuclear bag intrafusal fibres, while both types are ‘slower’ than extrafusal fibres. Both nuclear chain fibres and nuclear bag fibres, however, probably show a gradation in activity related to the nature of the muscle in which they lie. The reader is advised to study figure 33 and its legend first, at the same time studying the plate figures to which reference is made in figure 33 b , then to read the portions of the Results in italics consecutively followed by the Discussion, finally studying the detailed Results. Further details of many of the illustrations and tables are available for reference in the Archives of the Royal Society.


1967 ◽  
Vol 46 (1) ◽  
pp. 63-84
Author(s):  
K. M. CHAPMAN ◽  
J. H. PANKHURST

1. Conduction velocities of individual afferent nerve fibres from tactile spines and proprioceptive campaniform sensilla have been measured in situ over the temperature range 5-42° C., in leg preparations of the cockroach Periplaneta americana. 2. Conduction velocities at 20° C. (u20) averaged 3.3±1.4 m./sec., ranging from 1.6 to 11.0 m./sec. 3. Temperature coefficients, expressed as Q10 for the interval 20-30° C., averaged 1.7±0.24, ranging from 1.3 to 2.6. 4. The length of the propagated disturbance is about 2-3 mm., and is nearly temperature-independent. 5. Fibre diameters, estimated from conduction velocity, must be about 10 µ. 6. There is no correlation between conduction velocity and distance from the sensillum to the thoracic ganglion. Conduction delays in fibres conducting within one standard deviation of mean u20 range from about 2 to 15 msec., from the most proximal to the most distal tactile spines. 7. The effect of conduction delay on temporal and spatial sensory encoding is probably unimportant from a behavioural point of view. It contributes a factor of the form exp(-sd/u) to the sensory transfer function, and may be appreciable at upper physiological frequencies of impulse frequency modulation.


1948 ◽  
Vol s3-89 (6) ◽  
pp. 143-185
Author(s):  
D. BARKER

A study of the morphology and innervation of muscle-spindles from the quadriceps of the rabbit and cat has shown that: 1. The intrafusal muscle-fibres do not subdivide in their course through the spindle, as is maintained in some descriptions, but retain their individuality from pole to pole. 2. There is no constant feature which is characteristic of one pole of a spindle and not the other. A distinction can be made between the proximal and distal ends only when it is possible to orientate the spindle according to the proximal and distal ends of the muscle. The extreme ends of the spindle are attached indifferently to extrafusal endomysium, tendon, or perimysial connective tissue. 3. In the equatorial region each muscle-fibre of the spindle contains a dense aggregation of spherical central nuclei (‘nuclear bag’). On either side of this aggregation oval nuclei are disposed in the form of a chain within a central core of protoplasm (‘myotube region’). The nuclear bag is devoid of cross-striations and presumably non-contractile. The two polar portions of the muscle-fibre on either side of the bag are striated and each receives a motor innervation; hence they are presumed to function as independent contractile units. 4. The number of end-plates possessed by a spindle is approximately double its number of intrafusal muscle-fibres, with half the total number of end-plates situated at each pole. The ratio is rarely exact, since one polar half of an intrafusal fibre frequently bears two end-plates; these are innervated by nerve-fibres which retain their individuality as far as they can be traced back from the spindle. Both small nerve-fibres (3-4 µ in gold chloride preparations) and relatively large nerve-fibres (6-7 µ in gold chloride preparations) take part in the motor innervation of muscle-spindles, as was deduced on physiological grounds by Leksell (1945). 5. An analysis of the sensory innervation has confirmed many of Ruffini's (1898) observations. Primary or ‘annulo-spiral’ and secondary or ‘flowerspray’ endings occur and they are innervated by independent nerve-fibres; it is suggested that Ruffini's terms ‘primary’ and ‘secondary’ be adopted since the descriptive terms cannot always be applied. In the rabbit the secondary ending is ‘annulo-spiral’ in form and differs little from the primary ending; in the cat it is more irregular and could be termed ‘flower-spray’. The primary ending is always present and is associated with the nuclear bags of the intrafusal muscle-fibres; in some instances its ramifications are more extensive and also entwine the myotube regions. The primary ending may be the only sensory termination present, or it may be accompanied by one or by two secondary endings. These are borne by the myotube regions of the musclefibres. In the rabbit's quadriceps and interossei, spindles with one primary and one secondary ending were the most frequent in the samples taken; in the cat's quadriceps spindles with one primary and two secondary endings were the most numerous. Both the primary and secondary nerve-fibres invariably ramify so as to innervate each intrafusal fibre in the muscle-bundle. The two sensory terminations are often closely intercalated but do not overlap with one another to any great extent. As estimated from measurements made on fresh, silver, and gold chloride preparations the total diameter of the primary fibre lies between 8 and 12 µ, that of the secondary fibre between 6 and 9 µ. 6. Apart from small sympathetic fibres innervating the vascular supply of the spindle, other finer fibres may occasionally be seen ramifying within the walls of the capsule and over the polar regions. It is possible that they are somatic sensory fibres subserving the sensation of pain. 7. The nature of the reflex effects of the afferent impulses discharged by the muscle-spindle and tendon-organ is considered, and it is concluded that the balance of evidence indicates that the afferent discharge from the spindle is excitatory and that from the tendon-organ inhibitory to the motor neurones of the same muscle. However, the identification of the spindle as the receptor which excites the stretch reflex is found to rest largely upon equivocal evidence, its acceptance depending ultimately upon Matthews's finding (1933) of a considerable difference-in threshold between the spindle and tendon-organ in response to stretch. It is suggested that the large primary fibre innervating the spindle should be identified as the ‘stretch afferent’ rather than the smaller secondary fibre specified by Matthews, for the rapid con duction rate of the afferent discharge exciting the stretch reflex (Lloyd, 1943) indicates that sensory fibres of the largest diameter are employed. The functional significance of the secondary fibres is obscure and the specific reflex functions of the sensory fibres innervating both the spindle and the tendon organ clearly require further elucidation.


1986 ◽  
Vol 11 (1) ◽  
pp. 125-130
Author(s):  
M. SAKURAI

Sympathetic nerve fibres innervating the sweat glands in the skin are known to accompany sensory nerve fibres closely. Examination of sudorific function, therefore, is a useful aid in making a diagnosis of severed peripheral nerve and also provides valuable information on nerve function in the recovery stage following injury and surgery such as neurorrhaphy. Among the many methods which have been used clinically, the one employing bromphenol blue is thought to be the most simple and accurate.


1960 ◽  
Vol 7 (4) ◽  
pp. 725-742 ◽  
Author(s):  
Neil C. R. Merrillees

Lumbrical muscles of young rats were fixed with OsO4 and embedded in methacrylate for electron microscopy. The spindle capsule was found to be continuous with and similar in structure to the sheath of Henle surrounding the nerves supplying the spindle. The capsule consists of several closely applied concentric cytoplasmic sheets. Each sheet is about 1,000 A thick and has no fenestrations. Many caveolae and vesicles in the cytoplasm suggest active transport through the sheets. The periaxial space fluid contains much solid material. It is suggested that the capsule and periaxial space regulate internal chemical environment. The interfibrillar structures are less evident in the polar regions of intrafusal fibres than in extrafusal fibres. Simple motor end-plates occur on the polar regions of intrafusal fibres. In the myotube region of the intrafusal fibre a peripheral zone of myofibrils surrounds a cytoplasmic core containing nuclei, mitochondria, Golgi bodies, reticulum, and a few lipid-like granules. Naked sensory endings lie on the myotube "in parallel" with the underlying myofilaments. Naked processes of the primary sensory ending deeply indent the muscle plasma membrane and the underlying wisps of myofilament in the nuclear bag region. The plasma membranes of sensory nerve ending and intrafusal muscle fibre are about 200 A apart.


Sign in / Sign up

Export Citation Format

Share Document