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'Blebbing' of the nuclear envelope of mouse zygotes, early embryos and hybrid cells.

In the mouse zygote and in two-cell stage embryos the inner leaflet of the nuclear envelope of pronuclei and that of blastomere and polar body II nuclei evaginate, forming multiple blebs within the perinuclear space, which contains a granular material. Blebbing exists only in oocytes activated by sperm in vivo or in vitro, or parthenogenetically by treatment with ethanol or puromycin. The germinal vesicle and an interphase nucleus formed after treatment of the oocyte at metaphase I by puromycin do not form blebs. Formation of blebs is specifically located in the cell cycle. The burst of the blebbing activity occurs during the first half of the cell cycle in one-cell embryos and in the earliest interphase period in the second cell cycle. Blebbing ceases from the beginning of the third cell cycle. The occurrence in the cytoplasm of 'double-layered' vesicles containing granular material resembling bleb contents and the disappearance of blebs from the nuclear envelope by the end of the cell cycle provide evidence that blebs represent a step in the transport of some material from the nucleus to the cytoplasm. Ethanolic phosphotungstic acid does not stain blebs, suggesting the absence of basic protein in their contents. Blebbing can be induced in somatic (thymocyte) and embryonic (blastomere of 8-cell stage embryo) nuclei following cell hybridization with activated oocytes. Their response to the oocyte cytoplasm by initiating blebbing depends on: (1) the position of the host cell in its cell cycle at the moment of hybridization, and (2) the time spent by the foreign nuclei in the host cytoplasm following cell fusion. If donor nuclei are introduced close to the time of activation, they start to produce blebs at the time corresponding to the initiation of blebbing by the female pronucleus in the first cell cycle. If foreign nuclei are introduced a few hours after activation they must be incubated in the host cytoplasm for some time before initiation of bleb formation, provided that the host pronucleus has initiated blebbing by that time. The existence of blebbing in nuclei formed only after oocyte activation, and the timing and the general occurrence of this event during the earliest cleavage stages of almost every mammalian embryo, suggest that this special nucleocytoplasmic transport plays a specific role at the beginning of development.

Animals↗

2,8-Dihydroxyadenine renal stones in a 41-year-old man.

A case is presented of a 41-year-old man with a history of recurrent renal stones over 10 years. Analysis of the stone showed that, although it gave a positive reaction with the non-specific phosphotungstic acid test, uricase failed to identify any urate present. Analysis in a reference laboratory confirmed its composition as dihydroxyadenine. Patients who are homozygous for the rare autosomal-recessive adenine phosphoribosyltransferase deficiency, excrete large amounts of 2,8-dihydroxyadenine, which has poor solubility at normal urinary pH. Treatment with the xanthine oxidase inhibitor allopurinol induces a total cessation of stone formation. Increased awareness of the condition and knowledge of the limitations of some methods of laboratory analysis for renal stones should help to identify this type of stone and prevent renal damage.

Adenine↗

Perforin-like immunoreactivity in feline globule leukocytes and their distribution.

Distributional and immunohistochemical characteristics of the feline globule leukocyte (GL) were investigated by light microscopy. The GL, which contained eosinophilic large granules in the cytoplasm, was frequently found in the epithelia of the intestine and gall bladder, and less frequently found in those of the gastric pit, intrahepatic bile duct, and interlobular secretory duct of the pancreas. No GL was seen in the respiratory and urogenital organs. The GLs composed a homogeneous cell population including no mast cells according to the following histochemical stainings; phosphotungstic acid hematoxylin, alcian blue and peroxidase. The feline GL showed perforin-like immunoreactivity to anti-human perforin monoclonal antibody, but did not show histamine-immunoreactivity to anti-histamine polyclonal antibody. The results suggest that the feline GL is a lineage of large granular lymphocytes. The epitheliotropism and characteristics as granular lymphocytes of the feline GLs were similar to those of the intestinal gamma delta T cells of the mouse.

Animals↗

Improved method for enzymic determination of cholesterol in lipoproteins separated by electrophoresis on thin layer agarose gels.

The cholesterol of lipoproteins, separated electrophoretically on thin layer agarose films, is visualised and quantitated by incubating the gels in an enzymic reagent containing cholesterol esterase and cholesterol dehydrogenase. The individual fractions are quantitated by scanning densitometry. No sample pretreatment is necessary. All major fractions are detected readily. The accuracy of the determination is similar to that of ultracentrifugation. On average, imprecision is 3.1% for beta-, 7.0% for pre beta-, and 4.8% for alpha-lipoprotein cholesterol. Concentration and colour development are linear up to 8 mmol/l cholesterol in a given lipoprotein fraction. The results from the direct enzymic procedure for beta-, pre beta- and alpha-lipoprotein cholesterol are compared with those from quantitative lipoprotein electrophoresis after precipitation with phosphotungstic acid and bivalent cations and with those from different precipitation methods using dextran sulphate and polyethylene glycol. The new method has several advantages: high specificity; lack of dependence on the actual composition of the lipoproteins; lack of interference from coprecipitated proteins in the gel, e.g. fibrinogen or paraproteins; and insensitivity to lipolysis and high free fatty acid concentrations caused by heparin application or ageing of the specimen (at least for alpha-lipoprotein cholesterol quantitation). In its convenience and simplicity of operation, and the simple calculation of results, the method is similar to standard protein electrophoresis. The proposed method is therefore suggested as a standard method for elucidating lipoprotein disorders.

Cholesterol↗

Binucleate cell migration in the bovine placentome.

The ultrastructure of cow placentomes, collected between 37 and 260 days of gestation, was examined. The microvillar junction and binucleate cell granules were selectively stained by phosphotungstic acid. Fetal binucleate cells interrupted the microvillar junction and penetrated as far as the basement membrane of the uterine epithelium. The uterine epithelium included not only binucleate cells which contained the distinctive granules but also non-granulated binucleate cells with pyknotic nuclei at the microvillar junction. Binucleate cells with pyknotic nuclei were also seen within chorion cells. It is suggested that the normal function of a mature chorionic binucleate cell at all the stages of bovine pregnancy is migration into the uterine epithelium to release its granules and subsequent condensaton to a cell remnant which is phagocytosed by the chorionic epithelium.

Animals↗

The innermost layer of cementum in rat molars: its ultrastructure, development, and calcification.

The present study describes the ultrastructure of the innermost layer of cementum (ILC) in the rat molars and discusses its developmental process and calcification mechanisms. The following points are the main results of this study: The ILC is a thin layer, about 2.0 micron thick, intensely stained with hematoxylin but not stained by silver impregnation. Electron microscopically, it is composed of substances stained with ruthenium red and chronic phosphotungstic acid presumed to be proteoglycans and a few thin collagen fibrils. Periodontal fibers penetrate the ILC only a short distance, and do not reach the root dentin surface. The ILC begins to form on the root dentin surface, just after the disintegration of Hertwig's epithelial root sheath. At the same time, matrix vesicles and spherical bodies, which may be derived from the matrix vesicles, appear on the surface of the developing ILC. Dental sac cells show higher cell activities than the epithelial sheath cells. Observations support the view that the dental sac cells secrete the ruthenium red positive material. On the basis of the above findings, the ILC is suggested to be formed by the dental sac cells and calcified by the matrix vesicles derived from these cells. The ILC can be regarded as a specialized cementum between the root dentin and the cementum in the strict sense, serving the connection of the two tissues.

Animals↗

A cytochemical study of glycocalyx and the membrane cholesterol of rat glomerular podocytes.

In order to elucidate the cytochemical properties of rat podocyte's membranes, the authors studied the constituents and distribution of glycocalyx and membrane cholesterol. Chromic-phosphotungstic acid (Cr-PTA) stain combined with enzyme digestive tests was used for the glycocalyx analysis. A digitonin fixation method was applied for the detection of membrane cholesterol. On the whole surface of podocytes, glycocalyx showed a strongly positive reaction to Cr-PTA. In normal rats, the reactivity on the urinary surface above the slit membrane of the podocyte foot processes was decreased after treatments with neuraminidase, hyaluronidase and heparitinase. The reactivity on the basal surface below the slit membrane disappeared only after treatment with chondroitinase ABC. In Puromycin Aminonucleoside nephrosis (PAN) rats, the foot processes were effaced extensively. Though a highly positive reactivity of Cr-PTA was observed on the urinary surface of the podocytes, the basal surface reacted weakly. The positive reaction of the urinary surface was not affected by the treatments with neuraminidase, hyaluronidase and heparitinase, but the weak reaction of the basal surface disappeared completely through chondroitinase ABC treatment. The distribution of membrane cholesterol was clearly revealed by the digitonin fixation method, showing digitonin cholesterol complexes of localized trilamellar structures. In normal rat podocytes the complexes were found on the urinary surface, with only a few on the basal surface. In PAN rats the complexes were seldom noticed either on the urinary or basal surfaces. The heterogeneous distribution of glycocalyx and membrane cholesterol seen in normal rat podocytes are changed remarkably under nephrotic condition.

Animals↗

The subfibrillar arrangement of corneal and scleral collagen fibrils as revealed by scanning electron and atomic force microscopy.

The present study was designed to analyze the subfibrillar structure of corneal and scleral collagen fibrils by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Isolated collagen fibrils of the bovine cornea and sclera were fixed with 1% OsO4, stained with phosphotungstic acid and uranyl acetate, dehydrated in ethanol, critical point-dried, metal-coated, and observed in an in-lens type field emission SEM. Some isolated collagen fibrils were fixed with 1% OsO4, dehydrated, critical point-dried and observed without metal-coating in an AFM. Isolated collagen fibrils treated with acetic acid were also examined by SEM and AFM. SEM and AFM images revealed that corneal and scleral collagen fibrils had periodic transverse grooves and ridges on their surface; the periodicity (i.e., D-periodicity) was about 63 nm in the cornea and about 67 nm in the sclera. Both corneal and scleral collagen fibrils contained subfibrils running helicoidally in a rightward direction to the longitudinal axis of the fibril; the inclination angle was about 15 degrees in the corneal fibrils and 5 degrees in the scleral fibrils. These findings indicate that the different D-periodicity between corneal and scleral fibrils depends on the different inclinations of the subfibrils in each fibril. The present study thus showed that corneal collagen fibrils differ from scleral collagen fibrils not only in diameter but also in substructure.

Animals↗

Importance of immunoenzyme histochemical reaction in diagnosis of disseminated intravascular coagulation in human and animal material.

Renal tissues from 208 human necropsies were observed histologically for disseminated intravascular coagulation (DIC). The tissues were stained with hematoxylin-eosin, Mallory's phosphotungstic acid hematoxylin (PTAH) and cationic ferric hydroxide colloid stabilized with cacodylate (Fe-Cac), and tested by immunoenzyme histochemical (IEH) reaction for fibrin-related materials (FRMs). The use of the IEH method increased FRM recognition, and FRMs were detected in a total of 80 cases (38.5%). In 26 cases diagnosed clinically as DIC, FRMs were shown in 23 of the cases (88.5%). Thus, 57 patients with FRMs were clinically asymptomatic. In rats with DIC induced by endotoxin injection, glomerulus FRM was effluxed into the tubulus through the Bowman's capsule and was excreted into urine. The electric charge was reduced on the endothelial surface of the glomerular capillaries in both human and rat DIC. Under the scanning electron microscopy, the endothelial surface appeared coarse in the glomerular capillary and fibrin degradation was present. Our conclusions are: (a) PTAH is non-specific for FRMs, (b) IEH aids the pathohistological diagnosis of DIC, especially in asymptomatic forms including the compensated DIC state, (c) FRMs in tubuli suggest DIC, and (d) DIC is possibly initiated by a reduction in the capillary electric surface charge.

Animals↗

Molecular sieve in bovine descemets membrane as revealed by negative staining.

Descemet's membrane was isolated from the corneas of cows and observed by electron microscopy after negative staining with 1% phosphotungstic acid solution, pH 7.2. Ultrastructurally, bovine Descement's membrane had a very regular hexagonal pattern. Nodes were connected to the six others around each of them by thin filaments to form a hexagon. The distance between the nodes was approximately 120 nm, the diameter of the nodes approximately 30 nm, and the width of the connecting filaments approximately 10 nm. Bovine Descement's membrane was a molecular sieve composed of nodes and filaments substantiating our molecular sieve theory of basement membranes.

Animals↗

Potentiometric PVC membrane sensor for the determination of scopolamine in some pharmaceutical formulations.

A novel PVC membrane electrode for the determination of scopolamine ion based on the formation of an ion-association complex of scopolamine with the phosphotungstate counter anion as an electroactive material dispersed in a PVC matrix is described. The sensor shows a fast, stable, near-Nenstian response for 1 x 10(-2) mol dm(-3) to 1 x 10(-6) mol dm(-3) scopolamine at 25 degrees C over the pH range of 3 - 7 with a cationic slope of 54.5 +/- 0.5 mV/decade. The lower detection limit is 8 x 10(-7) mol dm(-3) and the response time is 15 -45 s. The selectivity coefficients for scopolamine relative to the number of interfering substances were investigated. There was negligible interference from the studied cations, anions, and pharmaceutical excipients. The determination of scopolamine in aqueous solution shows an average recovery of 100.0% and a mean relative standard deviation (RSD) of 1.5% at 500 microg/cm3. The direct determination of scopolamine in some formulations (scopolamine injection and eye drops) gave results that compare favorably with those obtained by the United State of Pharmacopoeia method. Potentiometric titration of scopolamine with sodium tetraphenylborate and phosphotungstic acid as a titrant was monitored with the developed scopolamine electrode as an end point indicator electrode.

Electrodes↗

Construction and analytical applications of plastic membrane electrode for oxymetazoline hydrochloride.

A new oxymetazoline (OM) ion-selective PVC membrane electrode based on the ion associate of OM with phosphotungstic acid was prepared. The electrode exhibits a linear response with a mean calibration graph slope of 57.16 mV decade(-1) at 25 degrees C within the concentration range of 1.96 x 10(-5) - 1 x 10(-2) M OMCl. The change in the pH within the range of 1.0 - 9.4 did not affect the electrode performance. The standard electrode potentials were determined at different temperatures and used to calculate the isothermal coefficient of the electrode (-0.001233 V). The electrode showed a very good selectivity for OM with respect to a large number of inorganic cations and compounds. The standard addition method and potentiometric titration were applied to the determination of (OM) with RSD not exceeding 1.19%.

Journal Article↗

An adult case with rhabdomyosarcoma of the liver.

An autopsy case of primary rhabdomyosarcoma of the liver in a 70-year-old man is described. The case could not be clinically differentiated from hepatocellular carcinoma. The tumor showed typical features of rhabdomyosarcoma; phosphotungstic acid hematoxylin (PTAH)-positive myofibrils and cross-striations were observed in the cytoplasm of highly plemorphic tumor cells.

Aged↗

Infantile myofibromatosis with a solitary lesion in the skull--case report.

The term "infantile myofibromatosis" was coined in 1981 to describe a rare type of soft-tissue tumor in infants. Solitary lesions are usual, but extremely rare in the skull. An infantile case involving a lesion in the left parietal bone is described. The patient was a 6-month-old girl admitted with a mass measuring 2 x 2 cm in the left parietal region. Skull x-rays showed an osteolytic lesion with a sclerotic margin in the parietal bone. Computed tomographic (CT) scans revealed a low-density mass with homogeneous enhancement. The tumor adhered to the dura and had destroyed the left parietal bone. Histological examination disclosed spindle-shaped cells arranged in short bundles and abundant vasculature. Phosphotungstic acid hematoxylin staining revealed longitudinal fibrils resembling myofibroblasts. This is the first report in which CT findings are described in a case of infantile myofibromatosis with a solitary lesion occurring in the skull.

Female↗

Ultrastructure of synapses in the lateral line canal organ.

The ultrastructure of afferent and efferent synapses on hair cells in the lateral line canal organ of hair cells in the lateral line canal organ of the fish Lota lota was studied, utilizing various fixation and staining techniques. New information was obtained about membrane-associated material, such as the presynaptic body and postsynaptic densities, by examining glutaral-dehyde-fixed material not subjected to osmication. Contrast was instead obtained either by section staining with uranyl acetate and lead citrate or by block impregnation with phosphotungstic acid (PTA). PTA-staining enhances the postsynaptic membrane of both the afferent and efferent synapses. It also stains the presynaptic dense projections at the efferent synapse and in a differential fashion, the afferent synaptic body. Secretion staining reveals a substructure in the feed of the afferent synaptic body, faintly seen but masked in osmicated tissue.

Animals↗

Effects of low and high relative molecular protein mass on four methods for total protein determination in urine.

Four commonly used methods for the determination of total protein in urine were compared. These were two biuret methods using different precipitants, a Ponceau S method and a Coomassie Brilliant Blue method. The protein content of the urines was also evaluated by sodium dodecylsulphate polyacrylamide gel electrophoresis. The biuret method with ethanolic phosphotungstic acid as precipitant correlated best with the Coomassie Brilliant Blue method (r = 0.944; p less than 0.001) but less well with the Ponceau S (r = 0.895; p less than 0.001) or biuret-trichloroacetic acid (r = 0.874; p less than 0.001) methods. For urines with normal electrophoretic protein patterns, the imprecise biuret-trichloroacetic acid method (cv = 18.5%) gave the greatest number of false high results (23 in 36 urines) as assessed by electrophoresis. False low results were common in low relative molecular mass (Mr) proteinuria, especially with the biuret-tricholoroacetic acid and Ponceau S methods. High Mr proteinuria rarely caused false low results. Discrepancies between methods appear to have resulted from incomplete precipitation of low Mr protein by trichloroacetic acid.

Azo Compounds↗

Proteoglycan association with collagen d band in hyaline articular cartilage.

Proteoglycans of canine articular cartilage were labelled for transmission electron microscopy using the cationic copper phthalocyanin dye, cupromeronic blue, in a critical electrolyte concentration method. Much of the proteoglycan appeared to be structurally unrelated to collagen but a small proportion was positioned close to fibrils. On demonstrating the characteristic collagen banding pattern with uranyl acetate and phosphotungstic acid, it was evident that proteoglycan interacted with collagen at the d band.

Animals↗