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Biomedical subjects

N Fujimaki

Publications and source records attributed to N Fujimaki.

25 records · Page 2Linked to original sources

Event-related potentials in silent speech.

Event-related potentials (ERPs) in silent speech using the vowel /a/ were recorded from 12 scalp electrodes and three electrodes monitoring eye and throat movements in eight subjects cued by one of two randomly lit light-emitting diodes (LEDs). The average silent-speech potential minus nonsilent-speech potential showed two significant scalp potential distributions--a positive difference in the occipital scalp area at a 0.30-s latency from the LED onset and a negative difference in the frontal scalp area peaking at electrode Fz at a 0.42-s latency. The occipital scalp potential may include an endogenous component like P3. Possible sites of neural activities underlying the frontal negative difference are discussed in relation to the topography of the scalp potential and functions involved in silent speech.

Adolescent↗

Ultrastructural changes of myotendinous junctions in tenotomized soleus muscles of the rat.

The effects of tenotomy on the ultrastructure of myotendinous junctions in the rat soleus muscle were studied by thin-section electron microscopy. When the soleus muscle was tenotomized at both distal and proximal ends, virtually all muscle fibers showed a characteristic alteration called central core lesion in their middle portions. The similar alteration was also found in the end portions of each muscle fiber. As early as 5 days after tenotomy, myofibrils at the fiber end were extensively disoriented and disintegrated with thickening of the Z-discs. The surface specializations, sarcoplasmic processes and invaginations of the fiber end were also altered in such a way that the sarcoplasmic processes retracted. The disintegration of myofibrils was most extensive at one week after tenotomy, often losing their association with the sarcolemma. The thickening and rod formation of the Z-discs at the fiber ends were prominent at 1 and 2 weeks. The thickened Z-discs and rod structures were never closely associated with the sarcolemmal undercoats, which were not significantly thickened. This suggests that the Z-disc and the sarcolemmal undercoat are discrete entities. Interestingly, the basal laminae were frequently seen to be separated from the sarcolemma forming free sheets, as the sarcoplasmic processes retracted. In the space surrounded by such free basal lamina were seen many vesicular or granular materials. At 3 and 4 weeks the fiber end showed a recovery process forming new myofibrils, as the sarcoplasmic processes grew long. Thus, the surface specializations of the fiber end were much more elaborate than those in the control muscle. At 5 and 6 weeks the myotendinous junctions returned to normal ultrastructure except that the surface specializations were still elaborated. These findings demonstrated that the myotendinous junction underwent a series of characteristic alterations and recovery of the surface specializations as well as myofibrils.

Animals↗

Confocal laser microscopy of dystrophin localization in guinea pig skeletal muscle fibers.

A confocal laser microscope was used to analyze the localization pattern of dystrophin along the sarcolemma in guinea pig skeletal muscle fibers. Hind leg muscles of the normal animals were freshly dissected and frozen for cryostat sections, which were then stained with a monoclonal antidystrophin antibody. In confocal laser microscopy, immunofluorescence staining in relatively thick sections could be sharply imaged in thin optical sections. When longitudinal and transverse sections of muscle fibers were examined, the immunostaining of dystrophin was seen as linearly aligned fluorescent dots or intermittent lines along the sarcolemma. In longitudinally cut muscle fibers, many fluorescent dots, but not all, corresponded to the sarcomere pattern, especially the I band. Sections cut tangential to the sarcolemma also showed a lattice-like pattern of longitudinal and transverse striations of fluorescent dots. Double staining for dystrophin and vinculin showed that the two proteins were not exactly colocalized. The end portions of muscle fibers were much more intensely stained with antidystrophin antibody than the central portions, following the contour of elaborate surface specializations at the myo-tendon junction. The staining pattern at the myo-tendon junction was also discontinuous. These confocal microscopic observations suggest that dystrophin may be localized in a nonuniform, discontinuous pattern along the sarcolemma and in some relationship with the underlying myofibrils.

Animals↗

The distribution and arrangement of microtubules in mammalian skeletal muscle fibers.

The distribution and arrangement of microtubules (MTs) in skeletal muscle fibers of the rat and mouse diaphragm were examined by thin-section electron microscopy. In the central portion of muscle fibers, most MTs ran longitudinally between myofibrils and beneath the sarcolemma, and some MTs ran transversely predominantly at the level of the I band, especially of the A-I junction, thus forming a lattice-like arrangement. At the fiber periphery, MTs were aggregated in the perinuclear region, from which they radiated to take a longitudinal course beneath the sarcolemma and to run in a transverse direction at the I-band level. In the end portion of muscle fibers, MTs were abundant and ran longitudinally into sarcoplasmic processes. MTs were often found to be spatially associated with membranous organelles. Quantitative analyses indicated that the longitudinally running MTs were remarkably more numerous in the peripheral zone of muscle fibers than in the deeper zones. The density of MTs in the central portion was almost the same in both red and white muscle fibers. The density was significantly higher at the fiber ends, though it varied considerably among different fibers. These results are discussed with special reference to the possible involvement of MTs in intracellular transport as well as structural support.

Animals↗

Digital ulcers/gangrene and immunoglobulin classes/complement fixation of anti-dsDNA in systemic lupus erythematosus patients.

The immunoglobulin classes/complement fixation of anti-dsDNA were studied in sera obtained from 17 systemic lupus erythematosus (SLE) patients with digital ulcers and/or gangrene (Group A); 13 SLE patients with leg ulcer, peripheral neuropathy or livedo (Group B); 24 SLE patients with Raynaud's phenomenon (Group C); and 18 SLE patients with active lupus nephritis (Group D). Antibodies to dsDNA of IgG and IgA classes were commonly present (often in high titers) in Groups A and D. However, complement fixation of anti-dsDNA was more common in Group D than in any of the other 3 groups.

Antibodies, Antinuclear↗