Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: EC:3.6.1.3 (ATPase)
65,361 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Fetuses were decapitated in one uterine horn in each of 14 sows at 45 d of gestation. Control (C) and decapitated (D) fetuses were removed by Caesarean section from three sows at 65 d of gestation (total of 10 D and 10 C fetuses), two sows at 85 d (six D and six C fetuses) and nine sows at 110 d (nine C and nine D fetuses) of gestation (Exp. 1). In Exp. 2, four to six fetuses were removed from each of two Ossabaw (O) gilts and three crossbred (C, Landrace X Yorkshire) gilts at 70 d of gestation, from three C and O gilts at 90 d of gestation and from three C and two O gilts at 110 d of gestation. In Exp. 1, one semitendinosis muscle was removed for histochemistry, whereas the contralateral muscle was removed and weighed. A medial portion of biceps femoris muscle was removed and used for histochemistry in Exp. 2. In both experiments, transverse sections (cryostat) of muscle were stained for lipid, glycogen (PAS) and the following enzymes: acid ATPase, NADH-TR, NADPH-TR, malate dehydrogenase (NAD- and NADP-dependent reactions; MDH), succinate dehydrogenase (SDH), alpha-glycerol phosphate dehydrogenase (with and without NAD; alpha-GPDH), isocitrate dehydrogenase (NAD dependent; ICDH), esterase, lipoprotein lipase and lipase. In Exp. 1, body and muscle weights of the two groups were not significantly different (P greater than .05) at 65 d of gestation, whereas D fetuses were smaller and had lighter weight muscles (P less than .05) at 85 d of gestation.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Enzyme histochemical studies in an ontogeny study of muscle development in Ossabaw and decapitated fetuses: cellular reactions. 401 46

Biopsy specimens from the masseter muscle of the miniature pig "Mini-LEWE" were analysed histochemically before and after unilateral occlusal disturbances. The percentages of different fibre types and the cross-sectional area of fibres were determined with the myosin-ATPase reaction after acid preincubation. The capillary membranes were visualized by means of modified PAS-reaction. There was demonstrated a significant increase from the percentage portion of ST-fibre types, especially of the side of occlusal disturbance, under experimental conditions. This indicates an increased isometric contraction of the masseter muscle. The size of FT-fibre types and the capillarity increase significantly on the side without occlusal disturbances, due to the dislocation of the masticatory efforts to this side. The masseter muscle fine structure is shown to be adapted good to the disturbed functional conditions. No significant side differences were found in the dry mass of the masticatory muscles, at the end of experiments.
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PMID:[Changes in the fine structure of the masseter muscle as affected by unilateral occlusal disorders]. 407 26

1. Six healthy males performed sustained contractions with different tensions related to their maximal voluntary contraction (MVC). The isometric exercise consisted of efforts to extend the knee when flexed at an angle of 90 degrees .2. Biopsy samples were taken from the lateral portion of M. quadriceps femoris before and after different periods (6-45 min) during a series of sustained contractions. Total glycogen content was determined on each muscle sample. In order to evaluate whether the glycogen depletion occurred preferentially in slow twitch (ST) or fast twitch (FT) fibres, serial sections of the muscle samples were stained for myofibrillar ATPase and glycogen (PAS reaction).3. In all experiments a selective glycogen depletion was observed. At low tensions, the ST fibres and at higher tensions the FT fibres became glycogen depleted. The critical tension at which this conversion in glycogen depletion from ST to FT fibres took place was 20% MVC.4. It is concluded that at sustained contractions of less than 20% MVC there is a major reliance upon ST fibres and above that level a primary dependence upon FT fibres. It is further suggested that restriction of blood flow and thus availability of oxygen at forces higher than 20% MVC may be the explanation for the present findings.
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PMID:Selective glycogen depletion in skeletal muscle fibres of man following sustained contractions. 427 38

The influence of sodium phenobarbital (PB) treatment on the sequence of N-nitrosomorpholine (NNM) induced focal preneoplastic lesions in the rat liver was investigated using a combined morphological and enzyme histochemical approach. Quantitative assessment of the different types of foci of altered hepatocytes visible in H&E sections after carcinogen application, namely the clear and acidophilic cell glycogen storage foci and mixed cell foci comprising glycogen storing cells and also more basophilic hepatocytes showing reduction in glycogen reserves, revealed a shift towards mixed cell character and greater size in PB-treated livers in comparison to those receiving NNM alone. Within the three dose levels of PB investigated (0.75, 0.075 or 0.0075 g/l drinking water) a clear dose dependence in appearance of mixed cell foci was apparent. Assessment of alterations in the activities of marker enzymes observed within preneoplastic foci was carried out by comparison of PAS preparations with sections reacted for glucose-6-phosphate dehydrogenase (G6PDH), gamma-glutamyl transpeptidase, glucose-6-phosphatase and adenosine triphosphatase. G6PDH proved the most consistent enzyme marker for small glycogen storage foci whereas larger foci of that type and mixed cell foci were associated with change in activity of all enzymes studied. The results are discussed in relation to the sequence of events occurring during hepatocarcinogenesis and the influence of PB on altered cellular populations. The applicability of enzyme markers is further considered in view of the question of heterogeneity within populations of preneoplastic foci.
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PMID:Enhancement of NNM-induced carcinogenesis in the rat liver by phenobarbital: a combined morphological and enzyme histochemical approach. 613 86

Chick biventer cervicis muscle fibres have been studied histochemically. Fast-twitch, focally innervated (alpha) fibres represent 70-80% of the total fibres in this muscles. Two histochemical profiles of slow-tonic multi-innervated (beta) fibres have been observed from embryonic life the adult (three-months) stage. These two slow-tonic types differ in the activity of their histochemically demonstrated myofibrillar ATPase after either acid or alkaline preincubation, and after formalin fixation. Both slow-tonic fibre types have a high oxidative metabolism and are PAS-negative. They are referred as to beta 1 and beta 2R fibre types (slow-tonic oxidative) in an expansion of Ashmore's nomenclature, and compared to avian slow-tonic sub-types that have been described in recent reports. beta 1 and beta 2 fibre types exhibit a similar pattern of innervation. Possible explanations of the origin of histochemical heterogeneity in multiple innervated fibres are discussed.
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PMID:Histochemical properties of the biventer cervicis muscle of the chick: a relationship between multiple innervation and slow-tonic fibre types. 616 96

In tissue decalcified with MgNa2EDTA at a neutral pH activity for ATPase can used be for demonstration of the vascular structures at the muscle-bone interface. The GOMORI method for alkaline phosphatase is only of value, when fresh unfixed tissue is to be examined. The azo-dye method for alkaline phosphatase failed to give satisfactory results, and so did the alpha-amylase PAS method. 5'-nucleotidase activity is present in both capillaries and in cells lining the surfaces of bones, while larger blood vessels are poorly stained.
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PMID:Methods for histochemical demonstration of vascular structures at the muscle-bone interface from cryostate sections of demineralized tissue. 616 24

Isometric muscle endurance was measured in fourteen physically active men without (placebo) and after acute oral administration of 160 mg propranolol (Inderal). Quadriceps muscle contractions were sustained at 65% maximum voluntary contraction (MVC) to exhaustion. Muscle biopsies were obtained from m. vastus lateralis at rest for subsequent histochemical analysis for myofibrillar ATPase and amylase-PAS in order to determine fiber type composition and capillary density. The time to exhaustion was shorter (p less than 0.01) during beta-blockade (0.82 +/- 0.22) min than placebo (0.90 +/- 0.23) min. Changes in endurance time, induced by beta-blockade, were not correlated with any of the muscle morphological or histochemical variables examined. It is concluded that muscular performance is impaired as a result of beta-blockade on muscle tissue irrespective of any concomitant change in central circulation.
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PMID:Isometric muscle endurance during acute beta-adrenergic blockade. 620 98

The differentiation of the lateral musculature in the elver stage of the European eel (Anguilla anguilla, L.) has been studied using histochemical staining techniques. Extracellular lipid deposits constitute 12% of the body cross-sectional area. Two fibre type may be distinguished on the basis of myofibrillar ATPase activity. Fibres with an alkaline-labile (pH 10.2) ATPase occur as a two-fibre layer around the trunk circumference, with invaginations along the horizontal septum and fin insertions. These pale-yellow fibres correspond to the slow ("red") fibres of other fish and comprise around 7% of the body cross-section (mean size, 167 micrometer2). Slow fibres show a moderate staining for PAS (glycogen), but a relatively weak reaction of Sudan black (lipid) and the aerobic enzyme markers succinic dehydrogenase (SDH) and cytochrome oxidase (COX). The bulk of the trunk muscle is composed of fast fibres (68%; 328 micrometer2). These are characterised by an alkaline (pH 10.2)-stable ATPase activity, and their innervation. Each fibre is innervated by a single "en-plaque" type endplate at one myoseptal end. Fast fibres adjacent to the slow fibre layer (2-4 fibres deep) show a moderate staining for PAS and a weak reaction for SDH and COX. Deeper regions show a wide range of fibre size, with about 5% being greater than 1,400 micrometer2. Fibres greater than 200 micrometer2 show no significant staining for glycogen, lipid, SDH, or COX. Small fast fibres less than 120 micrometer2 (up to 5% of the white muscle mass) show a strong staining reaction for PAS and a slight reaction for SDH and COX activities. Parameters of vascularisation were calculated from low-magnification electron micrographs (x 1,900). The number of capillaries/fibre and % fibre perimeter in contact with capillaries were, respectively, 0.98, 6.33% (slow fibres); 0.33, 1.96% (superficial fast fibres); and 0.12, 0.71% (deep fast fibres). These values are low in comparison with other fish species. It is suggested that the low aerobic capacity of elver slow muscle reflects a relatively restricted aerobic scope for activity associated with the anguilliform mode of locomotion.
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PMID:Muscle fibre differentiation and vascularisation in the juvenile European eel (Anguilla anguilla L.). 627 91

The authors subjected peripheral blood smears of Torpedoes to cytochemical analysis of lipids, protein, neutral and acid polysaccahrides and of some enzymatic activities, i.e. adenosine triphosphatase (ATP-ase), acid and alkaline phosphatase, aliesterase and peroxidase. It was found that neutrophilic granulocytes are intensely PAS and aliesterase positive and weakly ATP-ase positive. Eosinophilic granulocytes show the presence of neutral polysaccharides in the matrix (which is PAS positive) and strong ATP-ase and acid phosphatase activities in the granules. Lymphocytes sometimes contain weakly PAS and aliesterase positive granules. Monocytes show some small PAS positive granules and weak acid phosphatase and aliesterase activities. Thrombocytes contain some peripheral granules which are PAS positive and slightly ATP-ase positive. There are no transitional forms between the various cellular types. The results confirm the classification of leukocytes of Torpedoes into neutrophilic granulocytes, eosinophilic granulocytes, lymphocytes, monocytes and thrombocytes and contribute some informations about the histoenzymatic content of Elasmobranch leukocytes.
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PMID:Cytochemical identification of the leukocytes of torpedoes (Torpedo marmorata Risso and Torpedo ocellata Rafinisque). 636 Jan 39

The three main segments of the elephant epididymis were examined for the occurrence, in the spermatozoa and lining epithelium, of carbohydrates, neutral lipids and phospholipids, ATPase, alkaline phosphatase, succinic dehydrogenase, glucose-6-phosphate dehydrogenase, diaphorases, hydroxysteroid dehydrogenases, acid phosphatase and non-specific esterase. The most distinct feature of the carbohydrate content of the epididymis was a layer of acidic, alcian blue-positive glycoprotein over the luminal surface of the epithelium, particularly in the terminal segment. PAS-positive, diastase-resistant inclusions were also found throughout the epdidymis. Neutral lipid occurred as droplets above and below the nucleus in the epithelium of the middle segment, and as supranuclear accumulations in the terminal segment. All the enzymes except the steroid dehydrogenases were detected in the epididymal epithelium, and all except the steroid dehydrogenases and acid phosphatase were detected in the spermatozoa. There was considerable variation in the intensity of the cytochemical reactions in the epithelium, but not in the spermatozoa, in different regions of the epididymis. In general, the enzymes involved in active transport showed strongest reactions in the initial and terminal segments, the reactions in the stereocilia being the most intense. The enzymes involved in energy metabolism showed strongest reactions in the middle and terminal segments, with the activity being fairly evenly distributed throughout the cytoplasm of the principal cells. However, the two lysosomal enzymes which were studied showed quite different distributions: the reactions for acid phosphatase were strongest in the initial and middle segments, whilst the reactions for non-specific esterase were strongest in the middle and terminal segments. It is suggested that the initial segment is involved in absorptive and anabolic activity, the middle segment in anabolic activity, and the terminal segment (where spermatozoa are stored ready for ejaculation) in considerable metabolic activity and active transport of substrates across the epithelium.
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PMID:Studies of the deferent ducts from the testis of the African elephant, Loxodonta africana. II. Histochemistry of the epididymis. 644 36


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