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Biomedical subjects

K Takata

Publications and source records attributed to K Takata.

At least 271 records · Page 15Linked to original sources

Hormonal effect on glycosaminoglycans and glycoproteins in uteri of ovariectomized rats.

1. Glycosaminoglycans such as chondroitin sulfate A (or C), chondroitin sulfate B (dermatan sulfate), heparitin sulfate (heparan sulfate) and hyaluronic acid were identified as major glycosaminoglycan components in whole uteri as well as in uterine stroma of rats. Two types of sialoglycoproteins with different electrophoretic mobilities (fast- and slow-migrating) were detected in the glycosaminoglycan fraction from the luminal epithelia. 2. Treatment of ovariectomized rats with estradiol-17beta markedly increased the uterine contents of glycosaminoglycans. Chondroitin sulfate A (or C) was found to increase more than chondroitin sulfate B. Furthermore, it was found that the estrogen treatment specifically increases the fast-migrating sialoglycoprotein level in the luminal epithelia and results in the appearance of it in the uterine fluid. 3. Administration of progesterone to ovariectomized rats slightly increased the uterine glycosaminoglycan content without appreciable alteration of the uterine glycosaminoglycan pattern.

Animals↗

Effects of halothane on coronary and systemic circulations, myocardial metabolism and blood flow distribution within the canine heart.

Myocardial metabolism, blood flow distribution within the heart, and coronary and systemic circulations were observed during halothane anesthesia using 15 mongrel dogs. Pao2 and Paco2 were maintained near 100 and 40 torr respectively throughout the study. As arterial halothane content increased, most parameters of systemic circulation were depressed significantly. Coronary blood flow was reduced in parallel with myocardial oxygen consumption (MVo2) (r=+0.89, pless than0.001). Myocardial contractility decreased significantly as anesthesia deepened. MVo2 and myocardial CO2 production were reduced as arterial halothane concentration rose. Arterial-coronary venous difference in blood oxygen content remained unchanged even in deep stage. Lactate and pyruvate were continuously taken up by the myocardium, although the amounts of uptake were reduced as anesthesia progressed. Calculated excess lactate and redox potential did not show any signs of myocardial hypoxia even in deep halothane anesthesia. Among major hemodynamic parameters, left ventricular dp/dt max showed the closest correlation with MVo2. Microsphere injection method was used to observe blood flow distribution within the heart. Halothane did not influence the distribution significantly and I/O ratio of the left ventricular free wall remained near 1.0 during the study.

Animals↗

Mechanism of glucose transport across the human and rat placental barrier: a review.

Glucose is one of the most important substances transferred from the maternal blood to the fetal circulation in the placenta, and its transport across the cellular membranes is mediated by glucose transporters. Facilitated-diffusion glucose transporter GLUT1 is abundant in the placental barrier, as is the case in other blood-tissue barriers, where GLUT1 is present at the critical plasma membranes of the barrier cells. In the human placenta, the microvillous apical and the basal plasma membranes of the syncytiotrophoblast are rich in GLUT1, which molecule seems to be responsible for the transcellular transport of glucose across the placental barrier. In the rat placental labyrinth, two layers of syncytiotrophoblasts (termed syncytiotrophoblasts I and II from the maternal side) serve as a barrier. GLUT1 is abundant at the plasma membrane of syncytiotrophoblast I facing the maternal side, and the plasma membrane of syncytiotrophoblast II facing the fetal side. Numerous gap junctions, made of connexin 26, connect syncytiotrophoblasts I and II, comprising a channel for the transfer of glucose between them. GLUT1 in combination with the gap junction, therefore, seems to serve as the structural basis for the transport of glucose across the rat placental barrier.

Animals↗

Immunolocalization of centriole-associated striated rootlets in human submandibular gland cells with and without solitary cilia.

Using an antibody specific to striated rootlets, we investigated the immuolocalization of striated rootlets in cells constituting human submandibular glands. Striated rootlets were positively stained in all cell types constituting acini, intercalated ducts, striated ducts, and interlobular ducts, but their shapes were different. The mean lengths of striated rootlets were 1.46 +/- 0.49, 3.15 +/- 1.35 and 3.99 +/- 1.02 microm in acinar secretory cells, myoepithelial cells, and columnar cells of the striated duct, respectively. The rootlets were the longest in columnar cells of the striated duct, in which paired centrioles were located in the apical cytoplasm away from nuclei. These findings suggest that striated rootlets play important roles in the positioning of centrioles in the cell. 2-8% of striated rootlets in myoepithelial cells were associated with solitary cilia, but they were not associated with solitary cilia in acinar cells and columnar cells of the striated duct. These observations suggest that striated rootlets may be associated with centrioles under normal physiological conditions, without formation of solitary cilia.

Centrioles↗

Physiologic strains in the lumbar spinal ligaments. An in vitro biomechanical study 1981 Volvo Award in Biomechanics.

For understanding of the mechanical causes of low-back pain, knowledge of the biomechanics of the various spinal elements is essential. In this in vitro biomechanical study, in situ behavior of spinal ligaments of the L3-4 and L4-5 functional spinal units during physiologic activities was studied in a three-stage procedure. First, 72 load-displacement curves were obtained to determine the three-dimensional flexibility characteristics of the spinal units. Second, three-dimensional morphometric measurements were made of all the spinal ligament attachment points. Finally, a mathematical model was constructed to combine the flexibility and morphometric data and compute the ligament length changes and strains as functions of various spinal movements. In flexion movement, the interspinous and supra-spinous ligaments were found to be subjected to the highest strains, followed by the capsular ligaments and the ligamentum flavum. During extension, it is the anterior longitudinal ligament that has the maximum strain. In lateral bending, the contralateral transverse ligaments carried the highest strains, while the interspinous and supraspinous ligaments were relatively unstrained. In rotation, the capsular ligaments were by far the most strained ligaments.

Adult↗

Kinematics of lumbar intervertebral foramen.

This in vitro study provides original data regarding the three-dimensional movements of the intervertebral foramen as the spine undergoes normal physiologic motions. Three-dimensional flexibility characteristics of fresh cadaver functional spinal units were determined. The same spinal units were fixed and thinly sectioned to yield quantitated anatomy of the soft and hard tissues of the specimen in three-dimensions. The flexibility and anatomic data were stored in a computer. A mathematical model was utilized to combine the two data sets, resulting in a precise three-dimensional description of the movements of the intervertebral foramen. Changes in foramen height, width, and area were obtained as functions of major spinal motions. Preliminary results indicate differences in intervertebral foramen kinematics of nondegenerated and degenerated spines. Such changes may affect the nerve root adversely and hence participate in pain production.

Biomechanical Phenomena↗