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Spatial and temporal response properties of the vestibulocollic reflex in decerebrate cats.

Vestibulocollic reflex responses of several neck muscles in decerebrate cats were studied during angular rotations of the whole body in a large number of vertical and horizontal rotation planes, at frequencies from 0.07 to 1.6 Hz. Vestibulocollic responses were compared to eye muscle and forelimb muscle vestibular responses. Electromyographic activity was recorded by fine wires inserted in biventer cervicis, complexus, longus capitis, obliquus capitis inferior, occipitoscapularis, rectus capitis major, splenius, lateral rectus, and triceps brachii. At frequencies of approximately 0.5 Hz and above, neck muscle electromyographic response gains were sinusoidal functions of stimulus orientation within a set of vertical or horizontal planes, and a muscle's response phase remained constant across rotation planes, or reversed by 180 degrees. Response patterns at high frequencies were consistent with vestibulocollic reflex activation by semicircular canals through brain circuitry that modifies canal dynamics. At frequencies of approximately 0.5 Hz and above, the stimulus orientation in which a given neck muscle's response was maximal remained nearly constant across frequencies. Thus, we used responses to rotations at high frequencies to calculate axes of maximal response of each muscle in three-dimensional space. Lateral rectus, obliquus, and to a lesser extent, splenius and longus capitus were activated predominantly by horizontal rotations. Biventer was activated predominantly by pitch, triceps predominantly by roll, and complexus, occipitoscapularis, and rectus major significantly excited by rotations in all three coordinate planes. In some cases, at frequencies less than 0.5 Hz, neck muscle response phase varied depending on the vertical plane in which the cat was rotated, and the optimal response plane was poorly defined and varied with frequency. These responses indicated that, at some frequencies, neck muscle activity can result from summation of inputs with differing spatial orientation and dynamics (spatial-temporal convergence). Differences between responses to vertical and horizontal rotations suggested that low-frequency spatial-temporal convergence behavior of the vestibulocollic reflex during vertical rotations was due to convergent semicircular canal and otolith receptor inputs.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Cranial nerves of the coelacanth, Latimeria chalumnae [Osteichthyes: Sarcopterygii: Actinistia], and comparisons with other craniata.

We reconstructed the cranial nerves of a serially sectioned prenatal coelacanth, Latimeria chalumnae. This allowed us to correct several mistakes in the literature and to make broad phylogenetic comparisons with other craniates. The genera surveyed in our phylogenetic analysis were Eptatretus, Myxine, Petromyzon, Lampetra, Chimaera, Hydrolagus, Squalus, Mustelus, Polypterus, Acipenser, Lepisosteus, Amia, Neoceratodus, Protopterus, Lepidosiren, Latimeria and Ambystoma. Cladistic analysis of our data shows that Latimeria shares with Ambystoma two characters of the cranial nerves. Our chief findings are: 1) Latimeria possesses an external nasal papilla and pedunculated olfactory bulbs but lacks a discrete terminal nerve. In other respects its olfactory system resembles the plesiomorphic pattern for craniates. 2) The optic nerve is plicated, a character found in many but not all gnathostomes. Latimeria retains an interdigitated partial decussation of the optic nerves, a character found in all craniates surveyed. 3) The oculomotor nerve supplies the same extrinsic eye muscles as in lampreys and gnathostomes. As in gnathostomes generally, Latimeria has a ciliary ganglion but its cells are located intracranially in the root of the oculomotor nerve, and their processes reach the eye via oculomotor and profundal rami. 4) The trochlear nerve supplies the superior oblique muscle as in all craniates that have not secondarily reduced the eye and its extrinsic musculature. 5) The profundal ganglion and ramus are entirely separate from the trigeminal system, with no exchange of fibers. This character has an interesting phylogenetic distribution: in hagfishes, lampreys, lungfishes and tetrapods, the profundal and trigeminal ganglia are fused, whereas in other taxa surveyed the ganglia are separate. The principal tissues innervated by the profundal nerve are the membranous walls of the tubes of the rostral organ. 6) As in lampreys and gnathostomes, the trigeminal nerve has maxillary and mandibular rami. Unlike all other gnathostomes surveyed, the trigeminal nerve of Latimeria lacks a sizable superficial ophthalmic ramus. Thus, Latimeria lacks the well-developed superficial ophthalmic complex reported in most other fishes. As in gnathostomes generally, the maxillary ramus of the trigeminal nerve fuses with the buccal ramus of the anterodorsal lateral line nerve to form the buccal+maxillary complex. We reject the term 'Gasserian ganglion', which is often applied to the fused profundal and trigeminal ganglion of tetrapods. 7) The abducent nerve innervates not only the lateral rectus muscle (a character common to myopterygians) but also the basicranial muscle. As we previously reported, it is probable that the basicranial muscle of Latimeria is homologous to the ocular retracter muscle of amphibians.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Proprioception in extraocular muscles of the rat.

Stretch receptor afferents from extraocular muscles were found in the rat. Their first-order somata, responding specifically to eye muscle displacements, were restricted to the ipsilateral semilunar ganglion. Over a broad range of stimulus frequencies the sensitivity of receptors increased by a factor of 2.2 per decade with a mean sensitivity of 125 imp. s-1 mm-1 at 1 Hz.

Animals↗

Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle.

Recent experiments, showing that both cranial paraxial and splanchnic mesoderm contribute to branchiomeric muscle and cardiac outflow tract (OFT) myocardium, revealed unexpected complexity in development of these muscle groups. The Pitx2 homeobox gene functions in both cranial paraxial mesoderm, to regulate eye muscle, and in splanchnic mesoderm to regulate OFT development. Here, we investigated Pitx2 in branchiomeric muscle. Pitx2 was expressed in branchial arch core mesoderm and both Pitx2 null and Pitx2 hypomorphic embryos had defective branchiomeric muscle. Lineage tracing with a Pitx2cre allele indicated that Pitx2 mutant descendents moved into the first branchial arch. However, markers of both undifferentiated core mesoderm and specified branchiomeric muscle were absent. Moreover, lineage tracing with a Myf5cre allele indicated that branchiomeric muscle specification and differentiation were defective in Pitx2 mutants. Conditional inactivation in mice and manipulation of Pitx2 expression in chick mandible cultures revealed an autonomous function in expansion and survival of branchial arch mesoderm.

Animals↗

Analog VLSI-based modeling of the primate oculomotor system.

One way to understand a neurobiological system is by building a simulacrum that replicates its behavior in real time using similar constraints. Analog very large-scale integrated (VLSI) electronic circuit technology provides such an enabling technology. We here describe a neuromorphic system that is part of a long-term effort to understand the primate oculomotor system. It requires both fast sensory processing and fast motor control to interact with the world. A one-dimensional hardware model of the primate eye has been built that simulates the physical dynamics of the biological system. It is driven by two different analog VLSI chips, one mimicking cortical visual processing for target selection and tracking and another modeling brain stem circuits that drive the eye muscles. Our oculomotor plant demonstrates both smooth pursuit movements, driven by a retinal velocity error signal, and saccadic eye movements, controlled by retinal position error, and can reproduce several behavioral, stimulation, lesion, and adaptation experiments performed on primates.

Adaptation, Physiological↗

Medial transposition of the lateral rectus muscle in combined third and fourth nerve palsy.

Surgical treatment of combined third and fourth nerve palsy is a challenging problem in strabismology. Five of the 6 extraocular muscles are paralyzed, which leaves the lateral rectus muscle with no antagonist to counteract its activity and usually results in a maximal exotropia. The goal of surgery is to achieve orthophoria in primary position with limited ductions. Because some believe that a conventional recession-resection procedure will inevitably result in a drift back to exotropia,(1) several other methods have been proposed to treat this disorder. These include temporal mattress suture,(2) eye muscle prosthesis, (3,4) splitting and reattaching the lateral rectus muscle near the vortex veins,(5) and fixation of the eye with fascia lata.(6) Taylor(7) suggested using medial transposition of the lateral rectus muscle in a case of isolated third nerve palsy. We report the outcome of a procedure that included such a transposition for the treatment of combined third and fourth nerve palsy.

Eye Movements↗

Assessment of ocular counterroll during head tilt using binocular video oculography.

PURPOSE: According to recent literature, the presence and the amount of true compensatory ocular counterroll is still debatable. The purpose of the current study was to assess compensatory counterroll in response to lateral head tilt using a new noninvasive recording technique, and, furthermore, to find out whether the amount of counterroll is influenced by the presence or absence of spatial orientation. METHODS: Eye movement recordings were performed using the infrared three-dimensional video oculography (3D-VOG) technique. Objective cycloposition of five healthy individuals was measured in presumed primary position and in head tilt positions of 15 degrees, 30 degrees, and 45 degrees to the right and left. The same paradigm was performed under three viewing conditions: binocularly without spatial orientation and both binocularly and monocularly with spatial orientation. RESULTS: A consistent ocular counterroll corresponding to the amount of head tilt was observed in all subjects. Maximum torsional amplitude was 10 degrees at a 45-degree head tilt. The relative amount of compensation ranged between 13% and 22% of the actual head tilt, decreasing with increasing head tilt. Compensatory counterroll and torsional conjugacy between both eyes revealed minor differences between the experimental paradigms. Incomplete cycloductional reorientation in primary position after head tilt was detected in all subjects, regardless of the stimulus. CONCLUSIONS: A consistent compensatory ocular counterroll was demonstrated in response to static lateral tilting of the head in healthy individuals. The amplitude of counterroll and the gain of compensatory cycloversion were higher than has been generally reported. Infrared 3D-VOG technique was a reliable and comfortable method for the assessment of ocular cycloduction. It can be considered to be a promising tool for advanced evaluation of disturbances of the oblique eye muscles.

Adult↗

The total rehabilitation of Graves' ophthalmopathy.

The concept of enlarging the orbital space in some patients with Graves' ophthalmopathy is usually acceptable. Controversial, however, are 1. the indications for enlarging the space, 2. the sequence of therapy that is most successful in restoring the eyes to near normal, and 3. the value of enlarging the orbital space and its relationship to non-surgical alternatives. Since 1669 a personal experience with more than 600 eyes in over 300 patients using the transantral route to orbital decompression has accumulated. From the surgical experience plus exposure to other non-surgically treated patients, a concept of total management of Graves' ophthalmopathy has evolved. The technical aspects of decompression through the sinuses are straight forward. The key to a satisfactory operation is a complete transantral ethmoidectomy; a less than complete ethmoidectomy will eliminate a predictable result. Transantral decompresssion as a single procedure will not successfully palliate all aspects of Graves' ophthalmopathy. Eye muscles and lid procedures in a timely sequence may be needed to complete rehabilitation. Perfect eyes are seldom obtained but the goal of satisfied patients is realistic. This essay will emphasize technical aspects, theoretical advantages, as well as pitfalls and limitations of the transantral orbital decompression.

Adolescent↗

Medial rectus subgroups of the oculomotor nucleus ant their abducens internuclear input in the monkey.

Physiological experiments show that the abducens internuclear pathway is involved in the activation of only the medial rectus (MR) eye muscle. Previous anatomical experiments have shown that this pathway terminates in multiple foci within the oculomotor nucleus (OMN) of the monkey, and not only over the classical motoneuron subgroup. In this study the location of MR motoneurons in the monkey OMN is reinvestigated, and compared with the detailed pattern of terminations of the abducens internuclear pathway. The motoneurons were labelled by injections of retrograde tracer substances, HRP and [125I] wheat germ agglutinin (WGA), into extraocular muscles. Labelled MR motoneurons were found in three main divisions, called subgroup A, B, and C. Subgroup A corresponds mainly to the classical ventral MR subgroup. Subgroup B lies dorsal and caudal in OMN, occupying an area classically reserved for inferior rectus (IR). However, the representation of IR is shown to be further rostral in the dorsal OMN. Subgroup C is on the dorsomedial border of OMN. Its cells are significantly smaller than those of Group A and B. In addition C could be labelled independently of the other subgroups by small injections into the outer (orbital) layer of MR muscle. This indicates a functional difference between the subgroups. It is suggested that subgroup C may be important for the tonic component of MR activity, possibly convergence. The location of abducens internuclear terminals, labelled by the injection of tritiated amino acids into the abducens nucleus, corresponds exactly to the position of MR motoneurons. These experiments provide a new picture of the internal OMN organization, and support the physiological findings that the abducens internuclear pathway activates only MR motoneurons.

Abducens Nerve↗

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.

Walker-Warburg syndrome (WWS) is an autosomal recessive developmental disorder characterized by congenital muscular dystrophy and complex brain and eye abnormalities. A similar combination of symptoms is presented by two other human diseases, muscle-eye-brain disease (MEB) and Fukuyama congenital muscular dystrophy (FCMD). Although the genes underlying FCMD (Fukutin) and MEB (POMGnT1) have been cloned, loci for WWS have remained elusive. The protein products of POMGnT1 and Fukutin have both been implicated in protein glycosylation. To unravel the genetic basis of WWS, we first performed a genomewide linkage analysis in 10 consanguineous families with WWS. The results indicated the existence of at least three WWS loci. Subsequently, we adopted a candidate-gene approach in combination with homozygosity mapping in 15 consanguineous families with WWS. Candidate genes were selected on the basis of the role of the FCMD and MEB genes. Since POMGnT1 encodes an O-mannoside N-acetylglucosaminyltransferase, we analyzed the possible implication of O-mannosyl glycan synthesis in WWS. Analysis of the locus for O-mannosyltransferase 1 (POMT1) revealed homozygosity in 5 of 15 families. Sequencing of the POMT1 gene revealed mutations in 6 of the 30 unrelated patients with WWS. Of the five mutations identified, two are nonsense mutations, two are frameshift mutations, and one is a missense mutation. Immunohistochemical analysis of muscle from patients with POMT1 mutations corroborated the O-mannosylation defect, as judged by the absence of glycosylation of alpha-dystroglycan. The implication of O-mannosylation in MEB and WWS suggests new lines of study in understanding the molecular basis of neuronal migration.

Abnormalities, Multiple↗

[Surgical treatment of squint today. A status determination].

The treatment of choice for eso- and exodeviations with variable angle and/or convergence excess or eye muscle palsy with diplopia in the gaze field of the paretic muscle is--at least in Central Europe--posterior fixation sutures (Cüpper's suture operation). The scleral sutures are critical in this procedure. More reliable results can be obtained if the sclera is scarified meridionally at the suture site. Sufficient experience with guarantee stable results, even though the procedure is difficult. Tucking of the rectus muscles is gaining increasing acceptance as a less traumatic alternative to resection since with this procedure the vasculature of the insertion is conserved to some extent. Significant sursumduction or deorsumduction of 15 degrees or more and corresponding trochlear palsies can be treated by combined recess-tuck procedures on the oblique muscles (e.g., tucking of the superior oblique and recession of the inferior oblique in the same eye). A combined procedure is more effective than successive operations and side effects are minimized (e.g., consecutive Brown's syndrome). Differing amounts of vertical and torsional deviation can be treated with differential surgery on the margin of the oblique muscles. Dissociated vertical deviation should not be taken for sursumduction caused by inferior oblique overaction (reversed fixation test), as straightforward weakening of the inferior oblique muscles may have serious consequences in the former condition. Surgical treatment of Duane's syndrome should be based on the amant of head posture and on the angle of deviation and retraction in the primary position.(ABSTRACT TRUNCATED AT 250 WORDS)

Humans↗

Expression of eight distinct MHC isoforms in bovine striated muscles: evidence for MHC-2B presence only in extraocular muscles.

This study aimed to analyse the expression of myosin heavy chain (MHC) isoforms in bovine muscles, with particular attention to the MHC-2B gene. Diaphragm, longissimus dorsi, masseter, several laryngeal muscles and two extraocular muscles (rectus lateralis and retractor bulbi) were sampled in adult male Bos taurus (age 18-24 months, mass 400-500 kg) and analysed by RT-PCR, gel electrophoresis and immunohistochemistry. Transcripts and proteins corresponding to eight MHC isoforms were identified: MHC-alpha and MHC-beta/slow (or MHC-1), two developmental isoforms (MHC-embryonic and MHC-neonatal), three adult fast isoforms (MHC-2A, MHC-2X and MHC-2B) and the extraocular isoform MHC-Eo. All eight MHC isoforms were found to be co-expressed in extrinsic eye muscles, retractor bulbi and rectus lateralis, four (beta/slow, 2A, 2X, neonatal) in laryngeal muscles, three (beta/slow, 2A and 2X) in trunk and limb muscles and two (beta/slow and alpha) in masseter. The expression of MHC-2B and MHC-Eo was restricted to extraocular muscles. Developmental MHC isoforms (neonatal and embryonic) were only found in specialized muscles in the larynx and in the eye. MHC-alpha was only found in extraocular and masseter muscle. Single fibres dissected from masseter, diaphragm and longissimus were classified into five groups (expressing, respectively, beta/slow, alpha, slow and 2A, 2A and 2X) on the basis of MHC isoform electrophoretical separation, and their contractile properties [maximum shortening velocity (v(0)) and isometric tension (P(0))] were determined. v(0) increased progressively from slow to fast 2A and fast 2X, whereas hybrid 1-2A fibres and fibres containing MHC-alpha were intermediate between slow and fast 2A.

Analysis of Variance↗

Evidence for a chronic axonal atrophy in oculopharyngeal "muscular dystrophy".

We report on morphometric investigations of peripheral nerves in a woman, who died at the age of 69, presenting the classical symptoms of oculopharyngeal muscular dystrophy (OPMD) and a typical family history with several members (males and females) affected over three generations. Evidence for chronic axonal atrophy was found in peripheral nerves and especially in oculomotor nerves with severe axon loss in endomysial nerve twigs of extraocular, laryngeal, and tongue muscles. Whereas limb muscles presented features of neurogenic atrophy, severe changes of "myopathic" type were evident in extrinsic eye muscles, laryngeal constrictor, tongue, and diaphragma. However, we interpreted these changes as neurogenic in origin in view of the severe denervation found in those muscles. Our findings suggest that OPMD is a disease of primary neurogenic origin rather than a primary myopathic disorder.

Aged↗

Changes in the central representation of the extraocular muscles in the rat oculomotor nucleus after section and repair of the third cranial nerve.

The anatomical location of motoneurons controlling the extraocular muscles within the oculomotor nucleus was investigated by injecting retrograde horseradish peroxidase (HRP) into individual eye muscles in control rats and in rats submitted to intracranial section and repair of the oculomotor nerve 6 months previously. Compared to the controls, the operated animals showed marked changes in the somatotopic organization of the oculomotor subnuclei. The possible nature of this re-arrangement is discussed.

Abducens Nerve↗

Investigations of ocular changes, extraocular muscle thickness, and eye movements in Graves' ophthalmopathy.

UNLABELLED: The aim of this study was to evaluate ocular changes, to measure the thickness of extraocular muscles, and to assess eye movements in patients with active Graves' ophthalmopathy. MATERIAL AND METHODS: We examined 27 patients (18 women and 9 men) with Graves' ophthalmopathy. Their age ranged from 17 to 59 years; mean age was 42.7+/-2.9 years. The control group consisted of 30 healthy persons aged 43.6+/-2.6 years. All patients underwent a complete ophthalmic examination including best-corrected Snellen visual acuity testing, measurements of proptosis using Hertel exophthalmometer, echography using A/B mode Mentor Advent ultrasonic diagnostic imaging system, ocular motility, slit-lamp and ophthalmoscopic examination. RESULTS: The examination showed a significant increase of proptosis, periorbital edema in 66.67%, chemosis in 59.26%, injection of conjunctiva in 45.15% of patients. The majority of patients with infiltrative form of Graves' ophthalmopathy had a significant enlargement of medial rectus muscle (from 5.0 to 5.9 mm in 46.3%, from 6.0 to 6.9 mm in 22.22% of eyes) and inferior rectus muscle thickness (from 5.0 to 5.9 mm in 33.33%, from 6.0 to 6.9 mm in 24.07% of eyes), disturbances in upward (less than 30 degrees in 62.96%) and lateral eye movements (from 30 to 50 degrees in 77.78%). CONCLUSIONS: The results of ocular examination showed an increase of proptosis, periorbital edema, chemosis and injection of conjunctiva in patients with Graves' ophthalmopathy. Ultrasound investigations showed a marked increase in the volume of medial and inferior eye muscle. In patients with Graves' ophthalmopathy, the changes in ocular motility (upward and lateral gaze) were detected.

Adolescent↗

Sir Charles Bell on visual direction.

Helmholtz is usually credited with demonstrating the relationship between the perception of visual direction and eye muscle activity: he said that directional judgements resulted from the effort of will involved in altering the position of the eyes. However, Bell reached the same conclusion many years earlier, primarily on the basis of experiments with afterimages: an afterimage appeared to move with voluntary movement of the eye, but it appeared stationary when the eye was moved passively.

Afterimage↗

Scanning electron microscopy of ciliary muscle of monkey eye.

The three-dimensional structure of the ciliary muscles of the cynomolgus monkey eye was studied by scanning electron microscopy after the treatment of the muscle in 8 N hydrochloric acid. The meridional muscle bundles in the outer part of the ciliary body were closely arranged and multilayered, extending in a straight anteroposterior direction from its anterior tips to the distal terminal. The anterior part of the muscle bundles consisting of compactly associated small muscle bundles appeared to have a smooth surface and formed a broad belt partially covered by fibrocytes. The anterior tips of the muscle bundles were divided into slender bundles which were connected to the trabecular sheets. The distal terminal part of the muscle bundles tapered markedly in thickness and split into fine bundles resembling a brush, showing a firm fixation in the surrounding stroma of the ciliary body. In the anterior part of the ciliary muscle, the muscle bundles internally situated divided into two branches forming a Y-shape in their extension in the straight anteroposterior direction. The divided branches merged with the branches from other muscles of the same kind and formed muscle sheets with a reticular pattern separated by the stroma of the ciliary body. These adjacent muscle bundles were arranged occasionally like parquetry work, indicating that the sheets appeared to consist of oblique muscles in the meridionally sectioned specimen. In the present study paired tips of V-shape in the anterior part of both the meridional and oblique muscles were not observed. Beneath the obliquely extending muscle bundles, circumferentially arranged muscle bundles were observed, but the interconnection with the other two groups of the muscle bundles was not demonstrated.

Animals↗