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Biomedical subjects

T Nagamine

Publications and source records attributed to T Nagamine.

292 records · Page 17Linked to original sources

Characteristics of auditory P300 in children: application of single trial analysis.

As, especially in children, cognitive function might vary from one stimulus to the other, even when the same target stimuli are presented in the oddball paradigm, we applied the single trial analysis adopting discrete Fourier transformation followed by inverse discrete Fourier transformation to the auditory P300 for the first time in children. In 9 children, age 9-13 years, a positive peak was clearly identified in approximately a quarter of the processed single sweep responses to target stimuli (single sweep P300), whereas it was observed less frequently for non-target stimuli. In 2 children of age 6 years, it was difficult to discriminate single sweep P300 from background EEG activities even in the processed data. As for the former group, the detection ratio of P300 in single sweep target responses ranged from 10.0 to 40.0%, and its mean latency and amplitude ranged from 311 to 348 ms and from 31.7 to 41.5 microV, respectively. There was a significant correlation between average data and single sweep data in terms of the P300 latency. However, the amplitude of P300 in the average data bore no relation to the detection ratio, mean amplitude or variability of latency among single sweep P300s. As compared with adult data previously reported, the detection ratio of single sweep P300 was lower and the P300 amplitude was higher in childhood. P300 in children, at least past puberty, can be analyzed by using the single trial method, which is expected to provide more information about the development of human higher brain functions, especially cognitive function.

Adolescent↗

Immunohistochemical localization of bone morphogenetic proteins and the receptors in epiphyseal growth plate.

The expression of bone morphogenetic proteins (BMPs) and BMP receptors (BMPRs) in the epiphyseal growth plate has not been clarified. In this study, we studied immunohistochemically the spatial and temporal localization of BMP-2/4, osteogenic protein-1 (OP-1, or BMP-7), and BMP receptors (BMPR-IA, BMPR-IB, and BMPR-II) in the epiphyseal plate of growing rats. The proximal parts of tibia in growing rats were observed. At 12 weeks after birth, BMP-2/4 and OP-1 were expressed markedly in proliferating and maturing chondrocytes. BMPR-IA, IB and II were clearly co-expressed in proliferating and maturing chondrocytes, and the expression was decreased in hypertrophic chondrocytes. At 24 weeks, the expression of BMP-2/4 and OP-1 was decreased, but BMPRs were still well-expressed in proliferating chondrocytes. The temporal and spatial expression of BMP and BMPR suggests that BMP and BMP receptors play roles in the multistep cascade of enchondral ossification in the epiphyseal growth plate.

Aging↗

The spatial and temporal immunolocalization of TGF-beta 1 and bone morphogenetic protein-2/-4 in phallic bone formation in inbred Sprague Dawley male rats.

In male rats and mice, the membranous bone is rapidly formed in the proximal segment (p-segment) of the os penis, and then endochondral ossification proceeds in the proximal half. The spatial and temporal patterns of expression of transforming growth factor-beta 1 (TGF-beta 1) and bone morphogentic protein-2/-4 (BMP-2/-4) were examined immunohistochemically until 14 days after birth and compared. BMP-2/-4 expression was weak in the mesenchymal condensation just at birth, and up-regulated in the membranous bone and cartilage 3 days after birth. BMP-2/-4 was strongly expressed in proliferating and mature chondrocytes 7 days after birth. At birth, TGF-beta 1 expression was diffuse and very strong in mesenchymal condensation. Thereafter, TGF-beta 1 expression was continuously strong in membranous bone and cartilage. Seven days after birth, TGF-beta 1 was actively expressed in proliferating chondrocytes. TGF-beta 1 and BMP-2/-4 seemed to act co-operatively. In particular, TGF-beta 1 appeared to strongly regulate immature stage and BMP-2/-4 may regulate the mature stage.

Animals↗

Immunolocalization of transforming growth factor-beta s and type I and type II receptors in rat articular cartilage.

The activities of TGF-beta s and their receptors (T beta R) in the articular cartilage have not been fully elucidated as yet. Temporal and spatial expression of TGF-beta s and their receptors were examined immunohistochemically in the articular cartilage of growing rats to clarify their role in chondrogenesis. TGF-beta 1, -beta 2 and -beta 3 were strongly expressed from 6 to 50 weeks in the superficial, transitional, and least mature zones. The expression of TGF-beta s in hypertrophic chondrocyte was weak except TGF-beta 1. T beta R-I and T beta R-II were co-expressed with the ligand in the superficial, transitional, and least mature zones throughout the growth phase. This study revealed that TGF-beta s in the articular cartilage plays a major role in the modulation of endochondral ossification ensuring the growth and maintenance of the chondrocyte lineage in articular cartilage.

Activin Receptors, Type I↗