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1.
  • 1.1. Lateral ciliary activity and DOPA decarboxylase were measured in the ctenidium of Crassostrea virginica (Gmelin).
  • 2.2. Activity of the lateral cilia is dependent upon branchial nerve (Paparo, 1985a,b) and on intracellular calcium homostasis (Baker, 1963; Rassmussen, 1970, 1971; Romero and Wittman, 1971; Blanstein et al., 1978).
  • 3.3. PTZ induced lamella morphogenesis in eytosomes with subsequent release of calcium into the cytosol. This cilio-inhibition was enhanced in the presence of additional calcium in the perfusate.
  • 4.4. Prolonged exposure to light also induces fully converted membranous eytosomes with subsequent production of a gradual lateral cilio-inhibition. Darkness produces the opposite effect, in that secondary membranous conversions of cytosomes are inhibited.
  • 5.5. In the presence of A-23187 (a calcium releasing agent), inhibition of lateral activity is produced, independent of cytosomal conversion.
  • 6.6. It is postulated that photic electrical and chemical stimulation of neuronal chromoproteins can lead to release of calcium from sequestered cytosomal stores which triggers a neuro-exocytosis of a neuroinhibitory transmitter, dopamine.
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2.
  • 1.1. The three sets of giant fibres in the nerve cord of Nereis virens are connected by both electrotonic and chemically transmitting junctions.
  • 2.2. The paired laterals and paramedials are connected to their partners by electronic junctions. The laterals are also electrically coupled to the median giant fibre.
  • 3.3. The laterals are connected to the paramedials by an excitatory chemical synapse, while in the anterior segments the paramedials provide an inhibitory input to the median giant fibre.
  • 4.4. Afferent input to the giant fibres through the segmental nerves two and four is excitatory, except that to the median fibre in the caudal segments.
  • 5.5. There is no evidence of the segmental origin of the lateral giant fibres, either in the form of macrosynapses or segmental cell bodies.
  • 6.6. The median giant fibre originates from two groups of cell bodies in the sub-oesophageal ganglia.
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3.
  • 1.1. A simple procedure for isolation of high molecular weight genomic DNA, and RNA, from Streptococcus sobrinus OMZ176 is described.
  • 2.2. Cell cultures were grown aerobically for 10 hr.
  • 3.3. Spheroplast formation and lysis was achieved by mutanolysin/lysozyme-dependent digestion of the cell wall, followed by N-lauroylsarcosinate-mediated lysis.
  • 4.4. Nucleic acids were isolated directly from cell-lysates using cesium-trifluoroacetate (CsTFA) densitygradient centrifugation.
  • 5.5. Three different centrifugation regimes were tested: self-generated density gradients in a fixed angle rotor; self-generated density-gradients in a swinging-bucket rotor; pre-formed density-gradients in a swinging-bucket rotor.
  • 6.6. Genomic DNA isolated by the CsTFA-procedure was found to have higher purity as compared to genomic DNA isolated in a conventional CsCl gradient.
  • 7.7. Isolated DNA was shown to be of a quality suitable for applications in molecular biology.
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4.
  • 1.1. The subcellular distribution of nine transition metals (plus four additional elements) was measured in the kidney tissue of the quahog, Mercenaria mercenaria.
  • 2.2. Elemental analyses of the subcellular fractions indicated three main patterns of metal distribution within kidney cells.
  • 3.3. Barium, iron, manganese and lead were associated primarily with kidney granules.
  • 4.4. Cadmium, copper, potassium and magnesium were found mainly in the cytosolic fraction.
  • 5.5. Calcium, phosphorus and zinc were found in all isolated fractions, probably reflecting the important roles that these elements play in bivalve metabolism.
  • 6.6. The organelle composition of the isolated subcellular fractions was determined using marker enzyme assays and microscopic techniques.
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5.
  • 1.1. In smooth muscle of the guinea-pig stomach, intramural nerve stimulation evoked cholinergic excitatory junction potential in the fundus and non-adrenergic non-cholinergic inhibitory junction potential in the antrum, yet cholinergic contractions in both regions.
  • 2.2. This dissociation between electrical and mechanical responses was mainly due to different sensitivity of the membrane for depolarization to acetylcholine.
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6.
  • 1.1. Primary cultures of isolated sheep hepatocytes were used to characterize metabolic functions of liver: gluconeogenesis, ureagenesis and protein synthesis. The rates of all three metabolic activities were linear over a 20 hr culture period.
  • 2.2. Hepatocytes in the presence of glucagon increased the synthesis of urea by approx 30% (P < 0.05) and increased release of glucose into the medium by 60% (P < 0.05).
  • 3.3. In the absence of insulin, significantly more (35%; P < 0.05) glucose was released in the medium than in the presence of insulin.
  • 4.4. Results help evaluate the primary culture of sheep hepatocytes as an appropriate experimental model to study nutritional and hormonal regulation of liver in the ruminant species.
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7.
  • 1.1. A high percentage (53%) of isolated snails injected with prostate gland homogenates lay eggs.
  • 2.2. These egg masses consist of a few eggs which contain many nonviable oocytes.
  • 3.3. Preliminary experiments suggest that an egg-laying factor may be present in prostatic secretions.
  • 4.4. Snails bred in isolation from hatching, whether injected or not, occasionally lay viable eggs.
  • 5.5. This observation shows that self-fertilization or parthenogenesis is, in fact, possible in Helix aspersa Müller.
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8.
  • 1.1. The role of the visceral nerve in mediating the changes in heart rate associated with different behavioral patterns was investigated in Megalobulimus sanctipauli.
  • 2.2. The results of acute and chronic denervation experiments indicate that the visceral nerve has no excitatory or inhibitory tonic action on the heart of snails retracted into the shell, nor does it account for the increase in heart rate associated with the locomotion and feeding behaviors.
  • 3.3. These changes in heart rate are, probably, indirect effects of increased activity such as an increase in venous return.
  • 4.4. The visceral nerve is responsible for approximately 3/4 of the increase in heart rate associated with the first minute of extrusion.
  • 5.5. The small increase in heart rate observed in denervated animals is probably caused by an increase in venous return generated by muscle activity that forces the head and food out of the shell.
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9.
  • 1.1. Lipid peroxidation and membrane-related enzyme changes in the cerebral cortex of stroke-prone rats (SHRSP) and normotensive rats were examined at 5 and 20 weeks of age.
  • 2.2. In vivo formation of thiobarbituric acid-reactant substances was higher in SHRSP at 20 weeks of age and in vitro generation of free malondialdehyde was greater in SHRSP brains, both at 5 and 20 weeks of age, as compared with those in WKY.
  • 3.3. Membrane-associated enzymes such as Na/K-ATPase and 5'-nucleotidase activities were lower in 20-week-old SHRSP than in age-matched WKY.
  • 4.4. These results indicate how very prone the SHRSP brain is toward lipid peroxidation and subsequent membrane-related enzyme changes.
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10.
  • 1.1. Subcellular location of dihydropyrimidinase and NCβA-amidohydrolase2 was studied in a cell suspension culture of tomato (Lycopersicon esculentum cv. Lukullus) and in Euglena gracilis.
  • 2.2. By differential centrifugation, crude extracts were separated into ten fractions. Activities of both enzymes were found mainly in cytosolic fractions marked by EDH (tomato) and glu-6-P-DH (E. gracilis).
  • 3.3. A cytosolic location was also found by a 20–60% and a 17.5–30% sucrose density gradients.
  • 4.4. Using mitochondrial marker enzymes such as fumarase, SDH, CS and MDH, a mitochondrial occurrence of both enzymes or their release from mitochondria can be excluded by sucrose gradient centrifugations. This can also be achieved using purified mitochondria prepared from tomato cells by two subsequent sucrose gradients.
  • 5.5. A possible vacuolar location of dihydropyrimidinase and NCβA-amidohydrolase was excluded by comparing their activities in isolated protoplasts and purified vacuoles which were characterized by their marker enzyme α-mannosidase.
  • 6.6. A nuclear location of both enzymes and/or their release from the nucleus during procedures used cannot be excluded.
  • 7.7. The results are discussed in relation to subcellular location to other pyrimidine-metabolizing enzymes in plant cells.
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11.
  • 1.1. NADH-dependent isocitrate dehydrogenase has been purified 110-fold from the crude extract of the flight muscle mitochondria of Aldrichina grahami.
  • 2.2. The purification procedure involved Triton X-100 treatment of isolated mitochondria, column chromatography on DEAE-cellulose, Affi-gel blue, and P-cellulose.
  • 3.3. The purified enzyme was homogeneous by criteria of the polyacrylamide gel electrophoresis.
  • 4.4. The enzyme of the blowfly contains more acidic amino acids and less hydrophobic amino acids than that of pig heart.
  • 5.5. The molecular weight was determined to be 330,000 daltons. The subunit construction differs from ghat of mammalian isocitrate dehydrogenase.
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12.
  • 1.1. Treatment of isolated rat liver mitochondria with methyl methacrylate (MM) produced membrane disruption as evidenced by the release of citrate synthase, and changes in the ultrastructure of mitochondria.
  • 2.2. At concentration 0.1%, MM uncoupled oxidative phosphorylation as evidenced by stimulation of state 4 respiration supported either by pyruvate plus malate or succinate (+rotenone) and ATP-ase activity in intact mitochondria.
  • 3.3. At concentration 1% MM stimulated ATP-ase activity in intact mitochondria and succinate (+rotenone) oxidation at state 4 and was without effect on this substrate oxidation at state 3.
  • 4.4. MM inhibited pyruvate plus malate oxidation either at state 3 or in the presence of uncoupling agents.
  • 5.5. MM inhibited the NADH oxidase of electron transport particles at a concentration which failed to inhibit either succinic oxidase or the NADH-ferricyanide reductase activity.
  • 6.6. The data presented suggest that in the isolated mitochondria MM inhibits NADH oxidation in the vicinity of the rotenone sensitive site of complex I.
  • 7.7. The general conclusion is that MM may block an electron transport and to uncouple oxidative phosphorylation in rat liver mitochondria. The overall in vitro effect would be to prevent ATP synthesis which could result in cell death under in vivo conditions.
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13.
  • 1.1. The medial (MGF), lateral (LGF) and motor (RMS-2) giant neurons were confirmed as neural components in the earthworm Amynthas hawayanus polysynaptic reflex circuit by simultaneous potential recording and dye injection.
  • 2.2. The reflex was initiated from the mechanoreceptors when evoked by mechanical stimulation but electrical stimulation also evoked an antidromic response in the motoneuron.
  • 3.3. The primary reflex response propagates decrementally along both giant axons but directly evoked action potentials conduct in an all-or-none fashion.
  • 4.4. The secondary reflex response continues to propagate after the primary response disappears.
  • 5.5. A rhythmically discharging neuron of uncertain function was also identified.
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14.
  • 1.1. Molecular weight estimation and subunit analysis of four yolk phosphoproteins (PP1-PP4) in medaka (Oryzias latipes) eggs were performed.
  • 2.2. PP1 (Mr ≈ 210,000) and PP2 (Mr ≈ 180,000) were found to be heterodimers composed of subunits of 113,000 and 94,000 and subunits of 84,000 and 72,000, respectively.
  • 3.3. PP3 and PP4 [phosvitins of medaka (Murakami et al., 1990, Devl. Growth Differ.32, 619–627)], were monomeric phosphoproteins having mol. wts of about 40,000 and about 20,000, respectively.
  • 4.4. Lipid composition of the mixture of PP1 and PP2, vitellogenin and yolk were found to be almost the same. PP1 and PP2 are probably lipovitellins of medaka.
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15.
  • 1.1. Thermal stress, in vitro and in vivo, induced the synthesis of heat-shock proteins, HSP90, HSP70, and HSP23 in turkey leukocytes.
  • 2.2. HSP induction was both temperature- and time-dependent.
  • 3.3. Salinity-specific stress proteins were expressed with elevated osmolality in culture medium.
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16.
  • 1.1. The shell side of the mantle of Achatina fulica is several millivolts positive to the blood side in vitro.
  • 2.2. The electrical potential does not depend on Na+, Ca2+, Mg2+, K+ or HCO3 but requires the presence of chloride on the shell side.
  • 3.3. The potential difference and short-circuit current ranged from 3.0 to 30.0 mV and 15.0 to 75 μA/cm2 with averages at 10m V and 50 μA/cm2 respectively.
  • 4.4. The electrical gradient is reduced by 2,4-dinitrophenol, thiocyanate and furosemide but not by ouabain, CO2 or acetozolamide.
  • 5.5. It is suggested that the nature and mechanism of electrogenesis in Achatina parallels that of the Helix mantle.
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17.
  • 1.1. Transduction and transmission in catfish ampullary electroreceptors is mediated by sensory cells bearing microvilli, chemically mediating synapses, nerve terminals and one axon. Although some aspects still remain to be clarified, a number of properties have been found.
  • 2.2. Spike generation per seand the modulation of spike frequency by electrical stimuli behave differently with respect to a number of experimental factors.
  • 3.3. Stimulus current enters presumably through non-voltage-sensitive or non-specific ion channels.
  • 4.4. Fluctuations of the spike frequency may be used as a measure for proper functioning of this sense organ.
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18.
  • 1.1. Tissue-specific abundance of the capped small RNAs in the silkmoth Bombyx mori was compared using preparative immunoprecipitation with anti-trimethylguanosine antibody.
  • 2.2. The yields of total capped small RNAs from larval posterior silk gland, 1. early, 2. late in the fifth-instar, and 3. immortal ovarian-derived cells in culture, were determined to be 187, 50 and 218 ng, respectively, per mg of total cellular RNA.
  • 3.3. Separation of immunoprecipitated RNAs by polycrylamide gel electrophoresis, followed by densitometric analysis of the bands, allowed the quantitation of individual capped molecules.
  • 4.4. This analysis revealed tissue-specific patterns.
  • 5.5.|The data indicate that the total abundance of capped small RNAs in Bombyx is highest in rapidly-dividing cells.
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19.
  • 1.1. Biliverdin reductase from the liver of eel, Anguilla japonica was characterized and purified with a novel enzymatic staining method on polyacrylamide electrophoretic gel.
  • 2.2. This enzyme could use both NADPH and NADH as coenzyme. The Km of NADPH was 5.2 μM, while that of NADH was 5.50 μM.
  • 3.3. The optimum reaction pH for using HADPH as coenzyme was 5.3. That for NADH was 6.1. The optimum reaction temperature is 37°C.
  • 4.4. When NADPH was used as coenzyme, the Km of biliverdin was 0.6 μM. When NADH was used as coenzyme, the Km of biliverdin was 7.0 μM.
  • 5.5. The activity of the enzyme was inhibited by the concentration of biliverdin. Also, the potency of the enzyme was much less than that of the analogous enzyme isolated from mammals.
  • 6.6. This is a fairly stable enzyme with a mol. wt around 67,000. Its estimated pI was pH 3.5–4.0.
  • 7.7. This is the first time biliverdin reductase has been isolated and characterized from a vertebrate other than mammals. The property of it is quite different from that of mammals.
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20.
  • 1.1. The features of neoplasia which predict for drug responsiveness are rapid growth and/or inefficient repair of damage, especially to DNA.
  • 2.2. PDT has the advantage of yielding responses regardless of the growth fraction of a tumor, and repair appears to play only a minor role.
  • 3.3. While an entirely different spectrum of tumors can be targeted with PDT, the perhaps unavoidable accompaniment is that a new set of rules for efficacy will need to be established.
  • 4.4. The selectivity of PDT is based on the need for irradiation which can be directed, along with the short tissue half-life of the cytotoxic product, singlet oxygen. Sensitizers which target specific cellular organelles could promote PDT efficacy, if in vitro data (Woodbum et at., 1992b Photochem. Photobiol. 55, 697–704) can be translated into clinical practice.
  • 5.5. It remains to be established whether total drug distribution to neoplastic tissues or concentration in specific sub-cellular sites is the more important factor.
  • 6.6. Questions relating to the role of biodistribution as a factor in efficacy of PDT sensitizers of photosensitizers remain to be explored. Just as the political cartographers are grappling with changes in territorial boundaries of known lands, we continue to clarify the rules relating to PDT boundaries. In this regard, it is clearly important for determinants of pharmacokinetics and biodistribution to be evaluated and understood.
  • 7.7. Once clinical reports on the “second generation” agents are published, we may get a better picture, although it is not unusual for clinical reports to raise more questions than they answer.
  • 8.8. It seems safe to conclude that there is nothing “magic” about HPD, and that additional efficacious photosensitizers for PDT can be produced.
  • 9.9. If we find that a wide variety of different structures are useful in the clinic, a likely conclusion is that there are multiple mechanisms of tumor localization. Since the nature of neoplasia is so diverse, this possibility should not be surprising.
  • 10.10. In view of the finding, cited above, that liposomes show about the same degree of tumor selectivity as does Photofrin, it may be feasible to target any efficient photosensitizer for neoplastic tissues by development of an appropriate delivery system.
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