Dental pulp collagenase: initial demonstration and characterization.
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Biomedical subjects
Publications and source records attributed to K Iijima.
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Histochemical studies on the distribution of TPPase and G6PD in SON and PVN of rats have been conducted by using the new TPPase method, karyometry, and statistics under normal and thirsting conditions. All differences in nuclear volume among the 4 groups classified by the TPPase and G6PD reactions were significant after thirsting for 2 and 4 days, respectively. The intimate parallel relationship was found statistically between the GA shape and G6PD activity in neurons of both nuclei. These results may substantiate the usefulness of classification of neurons of both nuclei. These results may substantiate the usefulness of classification of neurons by the TPPase method on the LM level. They also suggest strongly that the GA shape may directly indicate its synthesizing activity, and that the complicate GA shape may correspond to the phase of vigorous synthesizing activity in the neuron. Both nuclei included some neurons whose GA appeared intact under activation. This suggests that secretory cycles of individual cells may proceed asynchromously under thirsting as well as normal conditions. The unique peak revealed by the curves of mean nuclear volumes of GA Type IV and G6PD. strongly positive groups only in PVN must be representative of phenomenon of exhaustion of PVN.
In order to ascertain the frequency of chromosome aberrations among newborn infants in Japan, a chromosome survey of a large number of newborn infants is in progress. A series of 10,270 consecutive newborn babies, 5,341 male and 4,929 female, have been screened for clinical manifestations of autosomal aberrations and for sex-chromatin and sex-chromosome aberrations. Chromosome studies were carried out on 185 infants with suspected chromosome aberrations. Of these, 23 had abnormal karyotypes, including 2 males with a 47,XXY complement, 1 female with 45,X complement, 3 males with a 47,XYY complement, 2 with trisomy 13 syndrome, 3 with trisomy 18 (including one mosaicism), 10 with Down syndrome (including 1 mosaicism), 1 with B5p partial trisomy, and 1 with Y-D translocation. Developmental studies of four XYY children and one 45,X girl are in progress.
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The difference of collagen producibility between 2 groups of skin fibroblasts from patients with Werner's syndrome with skin change and with normal skin, and the difference of collagen accumulation to cell layer between skin fibroblast from Werner's syndrome and controls were studied.
A series of 3545 newborn males, born consecutively at a maternity hospital in the western suburbs of Tokyo and with no detectable physical abnormalities, were studied for fluorescent Y-chromatin. Buccal cell smears from each infant were screened. Cases with ambiguous results were subjected to a second test by blood smears, which were found to be more reliable. After the second test, chromosomal analysis was carried out in five infants: three had a 47,XYY karyotype; one, the karyotype 46,XY-D,t(D:Y) (Iijima et al., in preparation); and one, a normal male karyotype. The XYY karyotype occurred in 0.11% of newborn males in this series.
The frequency of Y chromatin, visualized as fluorescent bodies in cell nuclei from lymphocytes in blood smears, was significantly less in newborn males than in three-month-old male infants and adults. The frequency of Y chromatin-positive cells on day 0 was 36.16 +/- 9.11% and then increased daily. At one month after birth the frequency was 55.07 +/- 9.29%, which was not significantly different from that in adult males (57.08 +/- 5.97%).
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Detailed histochemical studies have been conducted on the distribution of thiamine pyrophosphatase (TPPase), L-gulonolactone oxidase (GLO), and NAD-linked xylitol dehydrogenase (XDH) in every component of the Locus coeruleus (LC) of healthy adult male Rhesus and crab-eating monkeys in order to clearify the morphology of the Golgi apparatus (GA) and its relation to biosynthesis of catechol-amines in this special nucleus of the primate (NA nucleus A 6 as defined in the Rhesus monkey by German and Bowden [1975]). Medium-sized neurons of both species of monkeys, which are considered to play an important role in the LC, were classified into 5 groups on the basis of morphological patterns of the GA. Many neurons of both species of monkeys were positive for the XDH test while some neurons of the crab-eating monkey as well as a few neurons of the Rhesus monkey were positive for the GLO reaction. The LC of both species of monkeys must be composed of metabolically one kind of identical medium-sized parasympathetic neurons whose GA may continously undergo 5 distinct phasic changes depending on the functional state of that cell. However, the GA changes its shape much more significantly even within each group of the 5 in the crab-eating monkey than in the Rhesus monkey. The GA Type IV may correspond to the catabolic phase of the GA during which biosynthesis of both catecholamines and vitamin C should be going on. Production of vitamin C may greatly help biosynthesis of catecholamines in LC. The difference in species is evident between the 2 kinds of monkeys studied in regard to the degree of their ability to synthesize these substances. The degree of the ability to synthesize vitamin C parallels the density distribution of Type IV neurons in LC whose GA often develops much more greatly in the crab-eating monkey than in the Rhesus monkey.
By means of liquid chromatography we investigated free amino acids in cerebrospinal fluid (CSF) (161 subjects) and in plasma (138 subjects) in various neurological diseases and in controls. A general increase in CSF amino acids was found in Group C (samples exhibiting both pleocytosis and increasing CSF protein concentration) and in "spinal canal block" and "neuro-Behçet's syndrome". Also, some abnormalities were detected in these groups with regard to changes in CSF cells, protein or IgG%. In the case of "Guillain-Barré syndrome" we noted an increase in CSF alanine, glycine, methionine, arginine and the branched-chain group. In "multiple sclerosis" an increase was evident in CSF alanine, in plasma alanine and arginine, and in the plasma: CSF ratio of tyrosine. In patients of "motor neuron diseases (MND)" CSF glutamic acid, alanine, histidine and arginine all indicated an increase, along with the plasma: CSF ratio of tyrosine. In Group C and in "neuro-Behçet's syndrome" glycine, methionine and lysine were lowered in the plasma: CSF ratio. Also, the ratio of valine in the former and histidine in the latter indicated a decrease. These results can be supposed to reflect either biochemical abnormalities of plasma and/or the CNS, or changes in the transport systems of the blood-brain barrier.
Aging properties is studied on Au-10 wt% Pt and Au-10 wt% Pt-0.5 wt% Fe alloys containing 0.2, 0.4 and 2.0 wt% Indium. The results obtained are as follows: 1) In added Au-Pt alloys. From the electrical resistances in the isochronal aging curves, 0.2 and 0.4 wt% Indium added alloys are age-hardenable between 350 degrees and 640 degrees C. Heterogeneous phase in founded in 2.0 wt% Indium added alloy by meanes optical microstructures. This phase is identified fcc Pt3In by meanes X-ray diffraction. 2) In added Au-Pt-Fe alloys 0.2, 0.4 and 2.0 wt% Indium added alloys are age-hardenable between 250 degrees and 620 degrees C. Grain boundary reaction accelerated in 2.0 wt% Indium added alloy, and hardness decreased by overaging. Precipitation of nodule is inhibited in 0.2 wt% Indium added alloy, and aging properties also increase.
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Detailed histochemical studies have been conducted on the distribution of various enzymes, including thiamine pyrophosphatase, alpha-glucan phosphorylase, hexokinase, glucose-6-phosphate dehydrogenase, aldolase, glycerol-3-phosphate dehydrogenase; menadion oxidoreductase, lactate dehydrogenase and succinate dehydrogenase in various components of the cerebellum of healthy adult male rats of the Wistar strain. The thiamine pyrophosphatase reaction showed the morphological patterns of the GOLGI apparatus characteristic for each kind of cells. The GOLGI apparatus is a simple network in stellate cells, but it can be classified into the same 5 categories in basket cells and GOLGI type II cells. The GOLGI apparatus in the latter 2 cell types appears to undergo cyclic changes. A few GOLGI type II cells have a supranuclear form (Type II) and some cells show disintegration and "budding-off" of the GOLGI apparatus. The GOLGI apparatus in PURKINJE cells can be classified into 4 categories including a perinuclear strand form (Type III), but most of them show randomly distributed granules and vesicles. Lightly stained networks are observable in astrocytes and oligodendrocytes. They do not show polarity in astrocytes whereas they have extensions in a few oligodendrocytes. BERGMANN glia may undergo cyclic changes indicating more advance differentiation than astrocytes and oligodendrocytes. Cerebellar glomerula show lightly stained networks with many fine granules. Granule cells, stellate cells, and basket cells are all poorly equipped equally with the EMBDEN-MEYERHOF (EM) pathway and with the hexosemonophosphate (HMP) shunt. GOLGI type II cells are richly equipped almost equally with both the EM pathway and the HMP shunt. All these neurons probably derive energy mainly from glucose in the circulating blood. PURKINJE cells may belong to the category of "usual neurons", because they are moderately equipped both with the EM pathway and the HMP shunt. However, they may derive their energy from the BERGMANN glia which have intense hexokinase activity but weak succinate dehydrogenase activity. The BERGMANN glia are more richly equipped with the HMP shunt than with the EM pathway and are rich in lactate dehydrogenase suggesting an "exceptional metabolic pattern". These glia may have active synthesizing ability. Astrocytes and oligodendrocytes are equipped with all the enzymes tested, and they show a tendency to surround the glomeruli. It is suggested that the glomerula may be surrounded by the glial sheaths with strong hexokinase activity, and that they may contain alpha-glucan phosphorylase, glucose-6-phosphate dehydrogenase, and glycerol-3-phosphate dehydrogenase in addition to the succinate dehydrogenase already reported. A few PURKINJE cells showed perinuclear concentrations of the reaction product only of succinate dehydrogenase at the sites of contacts between nucleoli and nuclear membranes. It is suggested that the nucleolus may receive adenosine at the sites of contacts between nucleoli and nuclear membranes...
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Detailed histochemical studies have been conducted on the distribution of various enzymes such as thiamine pyrophosphatase, alpha-glucan phosphorylase, hexokinase, glucose-6-phosphate dehydrogenase, aldolase, lactate dehydrogenase and succinate dehydrogenase in various components of the nucleus Edinger-Westphali, nucleus n. oculomotorii, nucleus ruber and nucleus niger of healthy adult male Wistar strain rats. The thiamine pyrophosphatase reaction showed the morphological patterns of the Golgi apparatus characteristic for each nucleus. The Golgi apparatus was well developed in the nucleus Edinger-Westphali, composing a network of highly fenestrated plates in the nucleus n. oculomotorii and nucleus ruber, and a simple network in the nucleus niger. These results indicate that the former three nuclei need a rich energy supply and argue against the possibility that the four nuclei have a secretory role. The neurons of the nucleus Edinger-Westphali may derive their energy mainly from glucose of the circulating blood, but glial cells may serve as energy donators to the neurons in the pars compacta of the nucleus niger, and the neurons of the other nuclei may derive energy from both sources. These conclusions are consistent with the morphological patterns of the Golgi apparatus.
The plasma disappearance rate (K) and transfer rate constants for the two compartmental system of Indocyanine Green (ICG) were calculated in visualized and nonvisualized cases of the biliary tract with hepatobiliary disease using drip infusion cholangiography (DIC). In nonvisualized cases with hepatocellular disorder K and the fractional hepatic removal rate mainly decreased, and in nonvisualized cases with cholelithiasis the fractional biliary secretory rate significantly decreased by DIC-A, utilizing it as a screening test. Three methods (B,C and D) of drip infusion cholangiography were established according to the result of the I-CG test. Through DIC-B, C- or -D in addition to DIC-A the visualization of the biliary tract significantly elevated in patients with hepatocellular disorder and cholelithiasis. These results were confirmed using 131I-iodipamide. In some cases the serum transaminase activity elevated, but the elevation was temporary.