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Query: UMLS:C0276640 (TEM)
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Rat lenses incubated in tissue culture medium (M 199) maintain their transparency for a long period of time. The soluble corticosteroid, solumedrol (methyl prednisolone sodium succinate) was added to the medium, at concentrations including the range expected during rejection episodes following organ transplantation (3.8 X 10(-9) M-3.8 X 10(-6) M). At the lowest level used (3.8 X 10(-9) M), five lenses of 12 became opaque following a 48 hr incubation, while at higher concentrations of solumedrol almost all lenses developed opacities. Addition of vitamin E to the medium resulted in partial prevention of the cataract as judged by the smaller proportion of lenses becoming opaque. Examination of the lenses by scanning and transmission electron microscopy (SEM and TEM, respectively), indicated that in untreated lenses the initial location of the cataract is at the anterior pole of the lens where a deepening area of degeneration formed, followed by a uniform subcapsular layer of degeneration spreading over the remainder of the lens. Damage at this location is not typical of most in vitro cortical cataracts. In the presence of vitamin E the extent of damage was less, involving, initially, an equatorial wedge of globular degeneration and spreading anteriorly and posteriorly in a thinner subcapsular layer. This type of damage was more typical of that seen previously for cataracts induced by cytochalasin D, elevated glucose and hygromycin B.
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PMID:Modeling cortical cataractogenesis. V. Steroid cataracts induced by solumedrol partially prevented by vitamin E in vitro. 634

Human platelets have been observed by scanning electron microscopy after spreading on glass substrates followed by brief incubation in 1 mM ZnCl2 and subsequent shearing with a jet of buffer. The surfaces of many cells in such preparations are noted to consist of a reticular meshwork similar in appearance to the membrane skeleton of erythrocytes. In some preparations the reticular network is partially or almost entirely disrupted revealing an internal trabecular cytoskeleton and in the central region of the spread cell, granules associated with the cytoskeletal matrix. These results confirm previous observations obtained in TEM and HVEM studies of platelets and in addition provide information concerning the relative disposition of the filament systems in such spread cells. Preliminary results from sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis of platelets and isolated platelet membranes suggest a basis for the effect of ZnCl2 on various platelet cytoskeletal and membrane components.
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PMID:The platelet reticular network. 654 84

The TEM-EDS bulk-tissue analysis procedure described involves: (1) low-temperature oxygen-plasma ashing of soft tissue specimens weighing greater than 20 micrograms in aluminum-foil crucibles; (2) the solubilization of the ash in 5 microliter 0.5N HNO3 containing a known quantity of cobalt as an internal, non-interfering reference element; (3) the spraying of the solubilized ash from glass microcapillary tubes onto thin carbon-collodion films mounted on titanium grids; (4) EDS analysis of individual microdroplets approximately 3 micron in diameter; (5) the quantitation of elemental concentrations from the element: cobalt intensity ratio by the "ratio model" technique. This technique was assessed and found to yield linear curves (greater than or equal to 0.999) for elements in 'artificial tissue' standards (concentration range = 5 - 340 mM kg-1 dry weight). The overall reproducibility of the technique is therefore quite good (e.g. error of 4.7% for P and K in 25 analyses) within the range of concentrations expected for most of the major biological elements encountered in vertebrate and invertebrate soft tissues. Absolute accuracy can be improved with quantitative procedures that account for peak-overlapping and escape peak contributions etc., so that the ultimate MDL for sodium may well be of the order of 1 mM kg-1 dry weight. The usefulness of the technique for the provision of basic biochemical information (especially in invertebrate systems which have received but meagre attention) is illustrated: (a) by comparing the calcium content of male and female blood-flukes (Schistosoma mansoni) in mixed-sex and unisexual laboratory infections; and (b) by determining the changes induced by daily injections of the drug Astiban on the element composition of female Schistosoma. We conclude that the technique can represent a useful multi-element detection facility which offers certain pertinent advantages over alternative microchemical techniques, such as atomic absorption spectrophotometry.
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PMID:The electron microprobe analysis of sprayed microdroplets of solubilized biological tissues: a useful preliminary to localization studies. 663 80

A conspicuous feature of freeze-dried cryosections of male Schistosoma mansoni is the presence of groups of electron-dense granules. X-ray analysis in the TEM of these granules shows them, in comparison with the adjacent cytoplasm, to contain significantly greater amounts of sodium and calcium. In glutaraldehyde-fixed material, these granules have been correlated with the membrane-bounded, electron-dense granules found within the axons of the peripheral nervous system.
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PMID:The demonstration of calcium in the axonal granules of the peripheral nervous system of male Schistosoma mansoni by X-ray microanalysis. 706 Jan 5

Normal audiograms were obtained from a group of behaviorally conditioned chinchillas. Following this the animals were injected with sodium salicylate. Temporary hearing losses were measured 1 1/2 hours after treatment. Animals were anesthetized and blood samples taken to determine salicylate levels. The animals were then decapitated and the temporal bones were examined by SEM and TEM. No morphological correlate was seen for temporary hearing losses which were generally in the neighborhood of 30-40 dB.
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PMID:Salicylate ototoxicity in the chinchilla: a behavioral and electron microscope study. 713 37

Retraction of the taut, trailing portion of a moving chick heart fibroblast in vitro is an abrupt dynamic process. Upon retraction, the fibroblast tail always ruptures, leaving a small amount of itself attached to the substratum by focal contacts. Time-lapse cinemicrography shows that retraction produces a sudden, massive movement of both surface and cytoplasmic material toward a cluster of focal contacts near the main body of the cell. The appearance of folds on the upper cell surface at this time and the absence of endocytotic vesicles are consistent with this forward movement. Retraction of the trailing edge, either occurring naturally or produced artificially with a microneedle, consists of an initial fast component followed and overlapped by a slow component. Upon artificial detachment in the presence of iodoacetate, dinitrophenol, and sodium fluoride, and at 4 degrees C, the slow component is strongly inhibited and the fast one only slightly inhibited. Moreover of the bundles of microfilaments oriented parallel to the long axis of the tail seen in TEM. Most of the birefringence is lost during the fast phase and the rest during the slow phase of retraction. Concurrently, the bundles of microfilaments disappear during the fast phase of retraction and are replaced by a microfilament meshwork. All of these results are consistent with the hypothesis that the initial fast component of retraction is a passive elastic recoil, associated with the oriented bundles of microfilaments, and that the slow component of retraction is an active contraction, associated with a meshwork of microfilaments.
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PMID:Mechanism of retraction of the trailing edge during fibroblast movement. 719 6

Gold particles of varying size which contain either 195Au of 198Au were prepared using white phosphorus or sodium citrate as the reducing agent. After coating with specific antibody to blood group A antigen or human IgG, these particles were used to determine the number of particles binding to the surface of A1 RBC's or rat RBC's to which human IgG had been attached. The number of particles binding to the surface of cells correlated with the number of antibody coated gold particles in the fluid bathing the cells as well as the number of antigen molecules on the cell surface. That is, the number of particles binding increased as the particle density of the suspension increased and as the cell surface antigen density increased. Under the conditions of the experiments, both blood group A antigen and human IgG appeared to be randomly distributed over the surface of the cells in TEM and SEM preparations. This approach permitted the quantitation of the number of gold particles bound per cell and at the same time, the examination of the distribution of the particles over the surface of the same cell population by TEM and SEM.
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PMID:Antibody coated gold particles containing radioactive gold in the demonstration of cell surface molecules. 728 19

Cholic acid (sodium cholate) and the other active ingredients of F-5 gel preparations in use for the impregnation of a new vaginal sponge (Protectaid) with contraceptive and anti-sexually transmitted disease properties, were assessed for their effects on human sperm motility and ultrastructure. Cholic acid (CA) produced an inhibition of motility which was both dose- and time-dependent. A complete suppression of motility was obtained at 30 s by a CA concentration of 1.25%. Nonoxynol-9 (NX9) compared with benzalkonium chloride (BZC) showed no significant difference at the concentration required (0.025%) to give a total inhibition of sperm motility after exposure for 30 s. The addition of F-5A gel containing 0.5% of each one of the spermicide ingredients (CA, NX9 and BZC) produced the total suppression of sperm motility within 30 s at a dilution of 1/50. Another preparation, F-5B gel, containing the spermicide ingredients at different concentrations (1.25% CA, 0.125% NX9 and 0.05% BZC) produced this same effect with a 1/10 dilution. Exposure of semen to a CA concentration of 1.25% or to 1/10 dilutions of F-5A gel for 30 s led to profound changes of sperm ultrastructure studied by scanning (SEM) and transmission (TEM) electron microscopy. SEM and TEM findings indicate that CA acts as a spermicide through its 'natural detergent' properties, damaging the outer plasma membrane of sperm cells. Protectaid formulations affect sperm motility and viability in a similar way.
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PMID:Effects of cholic acid and 'Protectaid' formulations on human sperm motility and ultrastructure. 786 64

The synthesis of beta-lactamase inhibitory activity of a series of sodium 6-[(1-heteroarylthioethyl-1,2,3-triazol-4-yl)methylene]pe nicillanate, 1,1-dioxides are described. Their activity was compared with tazobactam and sulbactam. The Z-isomers were more active than the E-isomers. The in vitro activity of the Z-isomers of the phenylthiadiazole derivatives (13a and 15a) was better than sulbactam against the tested beta-lactamases and comparable to tazobactam especially against TEM-2 and cephalosporinase. But their synergistic activity with five antibiotics was inferior to tazobactam.
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PMID:Synthesis and beta-lactamase inhibitory activity of 6-[(1-heteroarylthioethyl-1,2,3-triazol-4-yl)-methylene]penam sulfones. 792 91

To provide the prerequisite for long-term study of the inner ear related to structural and functional integrity, tissue of stria vascularis with spiral ligament was isolated from Wistar rat cochleas and cultured using the explant-culture technique. The following culture media were used: EMEM with Hepes buffer, hydrocortisone (400 ng/ml), transferrin (5 micrograms/ml). triiodothyronine (10(-9) M), cholera toxin (10(-10) M), insulin (5 micrograms/ml), and epidermal growth factor (10 ng/ml). To characterize the cells growing out from the explant, immunofluorescence with cytokeratin (cytokeratin 18) and ultrastructural examination with SEM and TEM were performed. The marginal cell function was investigated by expression of Na+, K(+)-ATPase antisera against beta 2 subunit of rat Na+, K(+)-ATPase and P-NPPase. We were able to maintain the cultured cells for 3 weeks or more. Monolayered marginal cells were observed beyond 14 days in vitro and the expression of cytokeratin 18 was especially enhanced. The cultured marginal cells were almost identical to in vivo cells both as regards ultrastructural features and Na+, K(+)-ATPase activity. The present results suggest that the primary explant culture technique is a reliable in vitro model of strial marginal cells. However, establishment of the cell line is needed for long-term study.
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PMID:Establishment of primary cell culture from stria vascularis explants. Morphological and functional characterization. 897 11


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