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Biomedical subjects

Takashi Okiji

Publications and source records attributed to Takashi Okiji.

9 recordsLinked to original sources

Immunoelectron microscopic analysis of CD11c-positive dendritic cells in the periapical region of the periodontal ligament of rat molars.

To increase understanding of structural and phenotypic characteristics of dendritic cells (DCs) in the periapical region of the periodontal ligament (PDL) of rat molars, we performed immunoelectron microscopy for CD11c, a previously untested DC marker. Results demonstrated that CD11c clearly recognized DCs, although it also labeled certain macrophage subpopulation(s). In the normal PDL, resident DCs that extended several long cytoplasmic processes from their oval to slender cell body were identified. When the PDL was bacterially challenged by three days of unsealed pulp exposure, relatively small, irregularly shaped DCs with many thin and short cytoplasmic processes, most likely representing newly recruited DCs, were detected. The ratio of DCs in CD11c+ cells was significantly higher than that in ED1 (anti-macrophages and DCs)-positive and OX6 (anti-major histocompatibility complex class II molecules)-positive cells in normal and challenged PDL.

Animals↗

Heterogeneity of dendritic cells in rat apical periodontitis.

Dendritic cells are important for the induction of T-lymphocyte-mediated immunity by acting as antigen-presenting cells. We have previously reported that dendritic cells are prevalent in the chronic non-expanding phase of rat apical periodontitis. To characterize these cells further, immunoelectron microscopy with three dendritic cell markers (CD11c, OX6, OX62) was conducted for samples from rat models of apical periodontitis. Dendritic cells were divided into two types (type I or type II). Most of the type I dendritic cells expressed CD11c, showed an irregular large profile, had typical cytoplasmic processes, and were recognized as the major dendritic cell population. Most of the type II dendritic cells expressed OX62, showed oval small profiles with a few thin short processes, and were sometimes observed infiltrating from blood vessels. Cell-to-cell contacts between type I dendritic cells and lymphocytes were the most frequently observed associations. These results suggest that dendritic cells are composed of heterogeneous populations that exhibit different phenotypes, morphologies, and maturation/differentiation/activation.

Animals↗

Odontoblast responses to GaAlAs laser irradiation in rat molars: an experimental study using heat-shock protein-25 immunohistochemistry.

Pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation applied to the tooth remains to be elucidated. This study aimed to evaluate the effect of the GaAlAs laser on odontoblasts using immunohistochemistry for heat-shock protein (HSP)-25, which labels mature and newly differentiated odontoblasts. The mesial surface of the upper right first molar of 8-wk-old Wistar rats was lased at an output power of 0.5-1.5 W for 180 s. The animals were perfusion-fixed at intervals of 6 h to 30 d after irradiation. At 6 h to 7 d, the intensity of HSP-25-immunoreactivity was found to be disturbed in the coronal odontoblast-layer in an energy-dependent manner. At 30 d, tertiary dentin with/without bone-like tissue was formed abundantly in the dental pulp. Statistical analysis revealed that the area occupied by the new hard tissues was significantly wider in 1.5 W-lased specimens than in 0.5 W-lased specimens. An intense HSP-25 immunoreactivity was seen in the odontoblasts underlying the tertiary dentin, whereas immunoreactivity was weak around the bone-like tissue. It was concluded that the GaAlAs laser may induce the formation of tertiary dentin by influencing the secretory activity of odontoblasts. However, higher energies may cause irreversible changes to the pulp, often leading to the formation of an intrapulpal bone-like tissue.

Animals↗

Evaluation of a new fluoride-releasing one-step adhesive.

In this study, a newly developed S-PRG (surface pre-reacted glass-ionomer) filler-containing one-step adhesive, called SI (SI-IB551, Prototype), was evaluated regarding its fluoride release behavior. As a result, fluoride ion distribution in the tooth structures and acid resistance of cavity margins were also evaluated. In addition, Absolute (a fluoride-releasing one-step adhesive; AB) was evaluated in comparison to G-Bond (a non-fluoride-releasing one-step adhesive; GB) which was used as a negative control. Concentration of fluoride released was measured using a fluoride ion selective electrode after immersion of each material in distilled water. Fluoride distribution in tooth-adhesive interfacial areas was examined with EPMA following cavity preparation in human premolars and having treated resin restorations with each material. To evaluate acid resistance, restored specimens were immersed in an acetic acid buffer (0.2 M, pH 4.5) for 12 hours and then the cavity margins were observed using scanning electron microscopy. Amounts of fluoride released from AB and SI were significantly greater than that from GB. Further, significant differences in fluoride release were detected between AB and SI. A layer of increased fluoride density was clearly detected at the enamel- and dentin-SI interfaces. In terms of acid resistance, an acid resistance zone was also formed adjacent to the tooth-adhesive interface of AB and SI specimens. However, in GB specimen, acid resistance zone was not observed. These findings suggested that one-step adhesives displayed a favorable fluoride release property, thereby contributing positively to inhibition of recurrent caries.

Acrylic Resins↗

Enamel micro-cracks produced around restorations with flowable composites.

In this study, enamel micro-cracks produced around flowable composite restorations were observed using a stereomicroscope and a scanning confocal laser microscope (SCLM). The effects of polymerization shrinkage, mobility of composite and polishing period after filling on the incidence of marginal enamel micro-cracks were examined. Enamel micro-cracks were observed on all of the composite restorations when the restoration was polished immediately after filling. Enamel micro-cracks distributed approximately parallel to the cavity margin and located 0.01-0.3 mm from the restored cavity margin. The occurrence of enamel micro-cracks was higher in conventional hybrid composite restorations than in flowable composites, and when polished 15 minutes after filling (as compared to 24 hours after filling).

Analysis of Variance↗

An ultrastructural analysis of the prototype single-step adhesive applied on enamel and dentin surfaces.

A new type of self-etching agent, the single-step adhesive, was developed. The purpose of this study was to investigate the difference in the ultrastructural features of enamel and dentin surfaces following application of the prototype single-step adhesive (EXM618, 3M, MN, USA). Extracted caries-free human premolars were used in this study. Occlusal enamels of teeth--to be used as cut surface specimens--were removed perpendicular to the long axis of the specimens. The mesial and distal surfaces of these teeth, on the other hand, were used as uncut surface specimens in the test. In addition, Mega Bond (Kuraray Medical Inc., Tokyo, Japan) and Xeno CFII Bond (Dentsply Sankin, Tokyo, Japan) were used as controls. After covering half of the tooth surfaces with nail varnish (for control), the other half of each surface was treated with one of the three test adhesives--EXM618, Mega Bond, or Xeno CFII Bond--according to the manufacturer's recommendations. Conditioned enamel and dentin surfaces (i.e., decalcified depth and rugged surface) were observed with a scanning confocal laser microscope (SCLM 1100, Olympus, Tokyo, Japan; henceforth abbreviated as SCLM). Based on the findings of this study, the prototype single-step adhesive EXM618 appears to be suitable for use in dental clinics.

Acid Etching, Dental↗

Modified usage of the Masserann kit for removing intracanal broken instruments.

The Masserann kit is a hollow tube device specially designed for the removal of intracanal metallic objects. This report describes some modifications in the usage of this device for effective removal of tightly bound intracanal broken instruments whose diameter is relatively large at the coronal end. The techniques described are: (1) modification of the extractor to ensure gripping by creating a wider space inside the tube; and (2) combined use of the modified extractor with an ultrasonic device and a surgical operating microscope. A clinical case demonstrating that these modifications resulted in successful retrieval of firmly wedged instruments is presented.

Adult↗

An experimental study on the vasoconstriction effect of calcium hydroxide using rat mesentery.

Calcium hyroxide has been used for eliminating persistent intracanal exudation. In order to address the mechanism behind this action, we investigated whether calcium hydroxide solutions cause the constriction of microvessels in the mesenteric microcirculation bed of rats. The exteriorised mesentery from anaesthetised rats was spread in a chamber, and arterioles, venules and capillaries were viewed under a digital microscope. Various concentrations of calcium hydroxide solutions were applied for 10 sec, and the diameter of the microvessels was recorded. In arterioles, calcium hydroxide solutions caused rapid and transient constriction. A statistically significant difference versus original diameter was detected 1 min after the application of 4.0 x 10(-3) mol/l and 1.0 x 10(-2) mol/l solutions (p < 0.05, one-way analysis of variance and Tukey-Kramer test). No statistically significant constriction occurred in capillaries and venules. It was concluded that the arteriolar constriction might be an explanation for the exudation-controlling effect of intracanal calcium hyroxide dressings.

Analysis of Variance↗