Sensory components facilitating jaw-closing muscle activities in the rabbit

Summary The role of oral and facial sensory receptors in the control of masticatory muscle activities was assessed from the effect of acute deafferentiation on cortically induced rhythmic jaw movements (CRJMs) in anesthetized rabbits. When a thin polyurethane-foam strip (1.5, 2.5 or 3.5 mm thick) was placed between opposing molars during CRJMs, masseteric activities were facilitated in association with an increase in the medial excursion of the mandible during the power phase. The effects varied with the pattern of CRJMs, and the rate of facilitation was greater for small circular movements than for the crescent-shaped movements. Furthermore, the response of the masseter muscle was greater in the anterior half of the muscle, where muscle spindles are most dense, than in its posterior half. It was also demonstrated that the response increased with an increase in the thickness of the test strip. In contrast, the activities of the jaw-opening muscle were not affected significantly. The duration of masseteric bursts increased during application of the test strip and the chewing rhythm tended to slow down. However, the latter effect was not significant. After locally anesthetizing the maxillary and inferior alveolar nerves, the facultative responses of the masseter muscle to the test strip was greatly reduced but not completely abolished. Lesioning of the mesencephalic trigeminal nucleus (Mes V) where the primary ganglion cells of muscle spindle afferents from jaw-closing muscles and some periodontal afferents are located, also reduced the facilitative effects. Similar results were obtained in the animals with the kainic acid injections into the Mes V 1 week before electrical lesioning of this nucleus. In these animals the effects of electrical lesioning of the Mes V could be attributed to the loss of muscle receptor afferents since the neurons in the vicinity of the Mes V were destroyed and replaced by glial cells, whereas the Mes V neurons are resistant to kainic acid. When electrical lesioning of the Mes V and sectioning of the maxillary and inferior alveolar nerves were combined in animals with a kainic acid injection into the Mes V, the response of the masseter muscle to application of the strip was almost completely abolished. From these findings, we conclude that both periodontal receptors and muscle spindles are primarily responsible for the facilitation of jaw-closing muscle activities. Furthermore, it is suggested that the transcortical loop may not be the only path producing this facilitation since similar effects were induced in animals with ablation of the cortical masticatory area (CMA), when the test strip was placed between the molars during rhythmic jaw movements induced by pyramidal tract stimulation.     

Tactile feedback contributes to consistency of finger movements during typing

Touch typing movements are typically too brief to use on-line feedback. Yet, previous studies have shown that blocking tactile feedback of the fingertip of typists leads to an increase in typing errors. To determine the contribution of tactile information to rapid fine motor skills, we analyzed kinematics of the right index finger during typing with and without tactile feedback. Twelve expert touch typists copy-typed sentences on a computer keyboard without vision of their hands or the computer screen. Following control trials, their right index fingertip was anesthetized, and sentences were typed again. The movements of the finger were recorded with an instrumented glove and electromagnetic position sensor. During anesthesia, typing errors of that finger increased sevenfold. While the inter-keypress timing and average kinematics were unaffected, there was an increase in variability of all measures. Regression analysis showed that endpoint variability was largely accounted for by start location variability. The results suggest that tactile cues provide information about the start location of the finger, which is necessary to perform typing movements accurately.     

Influence of event anticipation on postural actions accompanying voluntary movement

Summary The central organization of anticipatory postural adjustments was investigated by examining the influence of preparatory set on the temporal relationship between postural and arm (focal) muscle activation. Surface EMG was recorded from the right tibialis anterior, lateral gastrocnemius, anterior deltoid and posterior deltoid muscles when pushing or pulling on a stiff handle. Preparatory set was manipulated by informing the subject of the upcoming direction of responding with a 80, 50 or 20% certainty. This created high, neutral and low levels of preparatory set, respectively. All six subjects showed activation of postural muscles in advance of focal muscles for both push and pull responses. However, only three subjects showed the expected effect of preparatory set on reaction time performance, i.e., an increase of reaction time with decreasing response probability. For these three subjects, the time between the activation of postural and focal muscles was the same for the high and neutral levels of preparatory set, but increased with a low level of preparatory set. The increased postural-focal latency for the low preparatory set condition was due to a longer delay for the activation of the focal muscles but not the postural muscles. This finding suggests that anticipatory postural adjustments and the activation of focal muscles are triggered by separate motor commands.     

Relationship between saccadic eye movements and cortical activity as measured by fMRI: quantitative and qualitative aspects

We investigated the quantitative relationship between saccadic activity (as reflected in frequency of occurrence and amplitude of saccades) and blood oxygenation level dependent (BOLD) changes in the cerebral cortex using functional magnetic resonance imaging (fMRI). Furthermore, we investigated quantitative changes in cortical activity associated with qualitative changes in the saccade task for comparable levels of saccadic activity. All experiments required the simultaneous acquisition of eye movement and fMRI data. For this purpose we used a new high-resolution limbus-tracking technique for recording eye movements in the magnetic resonance tomograph. In the first two experimental series we varied both frequency and amplitude of saccade stimuli (target jumps). In the third series we varied task difficulty; subjects performed either pro-saccades or anti-saccades. The brain volume investigated comprised the frontal and supplementary eye fields, parietal as well as striate cortex, and the motion sensitive area of the parieto-occipital cortex. All these regions showed saccade-related BOLD responses. The responses in these regions were highly correlated with saccade frequency, indicating that repeated processing of saccades is integrated over time in the BOLD response. In contrast, there was no comparable BOLD change with variation of saccade amplitude. This finding speaks for a topological rather than activity-dependent coding of saccade amplitudes in most cortical regions. In the experiments comparing pro- vs anti-saccades we found higher BOLD activation in the "anti" task than in the "pro" task. A comparison of saccade parameters revealed that saccade frequency and cumulative amplitude were comparable between the two tasks, whereas reaction times were longer in the "anti" task than the pro task. The latter finding is taken to indicate a more demanding cortical processing in the "anti" task than the "pro" task, which could explain the observed difference in BOLD activation. We hold that a quantitative analysis of saccade parameters (especially saccade frequency and latency) is important for the interpretation of the BOLD changes observed with visual stimuli in fMRI.     

A quantitative analysis of the geometry of cat motoneurons innervating neck and shoulder muscles

The geometry of the somata and dendritic trees of motoneurons innervating neck and shoulder muscles was investigated by using intracellular injections of HRP. In general, these motoneurons did not belong to a homogeneous population of motoneurons. Differences in average primary dendritic diameter, number of primary dendrites, and other measures of dendritic tree size were found between different neck and shoulder motoneuron groups. Several indices of proximal dendritic tree size (number of primary dendrites, sum of dendritic diameters, Rall's dendritic trunk parameter, and the sum of dendritic holes) were weakly correlated with the diameter or surface area of the soma. Some of these correlations depended on the muscle supplied by the motoneuron. The total combined dendritic length ranged from 66,660 to 95,390 microns. There was a weak, but positive, correlation between the diameter of primary dendrites and combined dendritic length. This relationship varied from motoneuron to motoneuron. The diameters of all dendrites of three trapezius motoneurons were examined in detail. The total dendritic surface area examined ranged from 415,000 to 488,100 microns 2 and represented approximately 99% of the total neuronal surface area. Last-order dendrites showed a high degree (39.9%) of taper. Dendritic tapering, by itself, was a major factor in the decrease of the (sum of dendritic diameters)3/2 measured at progressively distal sites from the soma. Although few parent and daughter dendrites obeyed the "three-halves law," the average exponent was 1.57. The diameters of primary dendrites and dendritic surface area were weakly correlated. The correlation between dendritic diameter and combined dendritic length or surface area improved if the weighted average of the diameter of second-order dendrites was used as a measure of dendrite size. Second-order dendrites, whose branches terminated in different regions of the spinal cord, showed different relationships between dendritic diameter and combined dendritic length or surface area. Comparisons between the motoneurons examined in the present study and motoneurons innervating other muscles indicate that, although all spinal motoneurons share several common features (e.g., long dendrites, dendritic tapering), each motoneuron group has a set of unique features (e.g., soma shape, relationship between primary dendrite diameter and dendritic surface area). Thus, the rules governing motoneuron dendritic geometry are not fixed but depend on the species of the motoneuron.     

Are eye movement evoked potentials different from pattern reversal evoked potentials?

The averaged lambda wave elicited by saccadic eye movements across a checkerboard pattern has been reported to differ from checkerboard reversal evoked reponses, even when the electroencephalographic responses were corrected for the artefact caused by the movement of the dipole moment of the eye itself. Because of these differences it was suggested that the recording of the lambda wave might provide extra information in pathological circumstances. We performed experiments in which the parameters of the pattern (high contrast checkerboard pattern, 20 checks, large field 72 × 72 degrees) shift across the retina were carefully adjusted. For instance, eye movements were made across an integer and odd number of checks in order to mimic the pattern reversal. Furthermore, the timing of the pattern movement in the pattern reversal condition was adjusted so as to simulate the saccadic eye movement. The results seem to suggest that the reported dissimilarities between pattern reversal and eye movement evoked responses can be accounted for by the small differences of the retinal shift in the two conditions.     

The Influence of Drugs on Nasal Ciliary Movement

Drugs in nasal preparations, for local use as well as for systemic use, should not interfere with the self-cleaning capacity of the nose, effectuated by the ciliary epithelium. Many drugs and additives, however, have a negative effect on nasal ciliary function. Examples of ciliotoxic agents are lipophilic and mercuric preservatives, local anesthetics, antihistamines, propranolol, and absorption enhancers such as the bile salts. Cholinergic drugs and -adrenergic drugs exert a ciliostimulatory effect. It is the purpose of this review to summarize the present knowledge of ciliotoxicity of drugs and additives and to give recommendations for the use of ciliofriendly drugs in nasal preparations.     

Saccadic anomalies: vergence induces large departures from ball-and-socket behavior

The configuration of muscular forces, which maintains a given orientation of the eye, varies with vergence state. As a consequence, changes in vergence produce both static and dynamic violations of simple ball-and-socket behavior: during strong convergence, the entire eye is displaced temporally within its orbit at steady state by as much as 200 microns; and the axis of ocular rotation for small horizontal saccades is consistently displaced forward within the globe by an average of about 1 mm. These phenomena occur regardless of whether vergence is maintained by accommodation or by binocular disparity. Hence, systematic errors of as much as a full degree can arise in measurement of vergence movement, unless monitoring methods are used which are insensitive to translational motion. The observed displacement on the axis of rotation for saccades may be involved in subjective shrinkage of visual targets during convergence ("experimental micropsia ").     

全反式维甲酸对培养的大鼠动脉平滑肌细胞迁移的影响

目的 :研究全反式维甲酸 (ATRA)对培养的大鼠动脉平滑肌细胞 (VSMCs)迁移的影响。方法 :血管平滑肌细胞采用组织贴块法培养 ,ATRA(2 .5× 10 -6mol/L)分别作用经PDGF -BB(2 0ng/ml)和 10 0 %FCS趋化作用下的VSMCs,采用改良的Boydenchamber方法检测VSMCs的迁移活性。结果 :ATRA作用的VSMCs对PDGF -BB和 10 0 %FCS的化学趋化活性明显减弱。结论 :ATRA具有抑制VSMCs迁移的作用。