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1.
  • 1.1. Dab, Limanda limanda, exposed to nominal concentrations of 0 (control), 0.0032% (low) and 0.032% (high) sewage sludge in seawater for 12 weeks, were assessed for their immunological competence.
  • 2.2. No effect upon total blood leucocyte and erythrocyte numbers was found, although significantly fewer thrombocytes were seen in the high-exposure group.
  • 3.3. A decreased serum protein level was found in the high exposure group, but lysozyme and immunoglobulin levels showed non-significant differences between the groups.
  • 4.4. Melano-macrophage centres were also affected in the high-exposure dab, which had increased numbers in the spleen and kidney. No effect upon spleen weights or oxygen free radical production by splenocytes was noted. However, oxygen free radical production by kidney leucocytes was inhibited in the low-exposure dab.
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2.
  • 1.1. Chemical feeding stimulants for an herbivorous fish, Tilapia zillii have been determined by fractionation and bioassay of substances derived from a model food plant.
  • 2.2. Stimulation was produced by amino acids; glutamic acid, aspartic acid, serine, lysine and alanine produced the bulk of stimulatory activity.
  • 3.3. These amino acids are among the most abundant in the test plant, and are markedly different from the amino acids found to stimulate feeding in carnivorous fish.
  • 4.4. On the basis of these results, a chemically-mediated mechanism of feeding niche separation is postulated.
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3.
  • 1.1. A variety of haematological parameters were determined in adult Dasyurus viverrinus.
  • 2.2. Haemoglobin and red cell counts were high with a very low mean cell volume.
  • 3.3. Basophils are absent but the eosinophils contain small numbers of basophilic granules which may indicate a dual role for this cell.
  • 4.4. “Ring Form” leucocytes are present.
  • 5.5. Three types of red cell picture could be identified, some animals showing large numbers of spherocytes, spicule cells, and inclusion bodies.
  • 6.6. These cells resemble those found in some inherited human haemolytic anaemias but there was no evidence of haemolysis in the animals.
  • 7.7. An alkali resistant haemoglobin component is present.
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4.
  • 1.1. Phospholipase A activity was found in the culture broth of growing cultures of Streptococcus mutans strain 6715.
  • 2.2. The amount of enzyme activity was proportional to the cell density of the cultures.
  • 3.3. The enzyme had a pH optimum of 7.0 and was inactivated at temperatures greater than 45°C.
  • 4.4. The enzyme was Ca2+-dependent, since both EDTA and EGTA were inhibitory and Ca2+ was stimulatory.
  • 5.5. Analysis of the fatty acid products resulting from the enzyme's action on 1-palmitoyl-2-oleoyl phosphatidylcholine indicated the enzyme to be a phospholipase A1, (EC 3.1.1.32).
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5.
  • 1.1. Freshwater nonanadromous rainbow trout, Salmo gairdneri, were injected three times a week with either saline, 10μg cortisol/g, 1.0μg thyroxine/g or 10μg cortisol/g + 1.0μg thyroxine/g during a period of 28 days (12 injections). A separate group was derived as a subgroup from the thyroxine group on day 14 and received Cortisol + thyroxine from day 14 until day 28 (six injections).
  • 2.2. Gill chloride cell number and Na+/K+-ATPase activity increased by cortisol treatment, the changes being significant on days 7 and 14, respectively.
  • 3.3. Thyroxine treatment did not affect gill Na+/K+-ATPase activity or chloride cell number directly. Neither did it modify the stimulatory effect of cortisol on these parameters.
  • 4.4. Muscle water decreased in cortisol-treated fish and increased in thyroxine-treated fish, while no changes were observed in the combined hormone groups.
  • 5.5. No changes were observed in plasma chloride in any group during the experiment.
  • 6.6. The results demonstrate a putative role of cortisol in stimulating hypo-osmoregulatory mechanisms and suggest that thyroxine is without a direct or a supportive effect for cortisol action.
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6.
  • 1.1. Size and composition of sagittal otoliths from red drum, Sciaenops ocellatus (Sciaenidae), reared at various constant temperatures were compared with otoliths from wild-caught fish.
  • 2.2. Uncoupling of otolith growth and somatic growth in laboratory-reared fish was evident in otolith length, area, volume, weight, density, and organic fraction.
  • 3.3. Fish grown at low temperatures had significantly smaller and less dense otoliths having a greater organic content than fish of the same size grown at higher temperatures.
  • 4.4. Changes in inorganic elements were poorly related to temperature in laboratory-reared fish.
  • 5.5. The effect of temperature on otolith elemental composition was small relative to the effects of age and its associated physiological changes.
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7.
  • 1.1. Protein synthesis by GTP -supplemented yeast mitochondria is stimulated by a fraction of molecular weight less than 2,000 isolated from yeast high-speed supernatant (S-150).
  • 2.2. The low molecular weight fraction works independently of the respiratory chain as the stimulation effect is not cyanide-sensitive.
  • 3.3. Stimulation of mitochondrial protein synthesis by cytoplasmic factors is dependent upon the method of mitochondrial isolation.
  • 4.4. The low molecular weight stimulatory factor(s) are not reduced folate derivatives which supply formyl groups required for initiation of mitochondrial protein synthesis.
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8.
  • 1.1. The neuroendocrine caudodorsal cells (CDCs) of Lymnaea stagnalis are a network of about 100 electrotonically coupled neurones. The CDCs release multiple peptides, including an ovulation hormone, during a period of electrical activity, the CDC-discharge.
  • 2.2. In isolated brains, a similar period of electrical activity (the afterdischarge) can be induced in all CDCs by a period of intracellular repetitive suprathreshold stimulation of one CDC.
  • 3.3. In order to study the regulation of this electrical behaviour in the absence of electrical interactions and in a controlled environment, experiments were performed on CDCs in dissociated cell culture.
  • 4.4. Methods for isolation and cell culture are described. Cell cultures had long-term viability and outgrowth of neurities occurred under serum-free conditions.
  • 5.5. CDCs in cell culture maintained their capability of producing afterdischarges upon electrical stimulation. Cells in culture appeared more excitable than cells in the intact isolated brain.
  • 6.6. The characteristic responses of CDCs in intact isolated brains to acetylcholine and FMRFamide were preserved in cultured CDCs. Both agents induced a transient hyperpolarization of the membrane, inexcitability and inhibition of an ongoing discharge.
  • 7.7. In experiments where isolated CDCs were closely apposed, but physically separate, it was found that an afterdischarge in one CDC could induce a discharge in the other CDC.
  • 8.8. These results confirm previous results which showed that an excitatory factor is released from the brain during the afterdischarge (Ter Maat et al., 1988, Brain Res., 43, 77–82), and demonstrate that this excitatory factor is released from the CDCs themselves.
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9.
  • 1.1. Heparin stimulates the activity of nonactivated and activated skeletal muscle phosphorylase kinase in a Ca2+-dependent manner.
  • 2.2. The stimulatory effect of heparin on the activity of nonactivated phosphorylase kinase is also expressed in the presence of calmodulin and glycogen. Heparin acted in synergism with glycogen.
  • 3.3. Heparin increases the affinity of phosphorylase kinase to Ca2+ 5–12 fold depending upon the activation conditions.
  • 4.4. Ca2+ influences the stimulation of liver phosphorylase kinase by heparin in a similar way.
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10.
  • 1.1. The electric organ discharge (EOD) frequency modulations evoked by brief water vibration were analysed in the pulse-type fish Gymnotus carapo.
  • 2.2. The response consisted of a transient increase of the EOD frequency at short latency (30 msec). Response profiles were characteristic of the specimen and relatively independent on stimulus intensity.
  • 3.3. Conversely, they were dependent on stimulation sequence, showing a rapid decrement along successive stimuli and high temporal discrimination.
  • 4.4. The brief latencies indicate a relatively simple neural circuit.
  • 5.5. The response may be an electrolocation enhancement strategy for the detection of moving objects based on “sampling” the periphery at a higher frequency.
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11.
  • 1.1. Babesia hylomysci has an aminopeptidase and an acid endoprotease
  • 2.2. The amino-peptidase has properties very similar to the aminopeptidase in Plasmodium yoelii nigeriensis and P. chabaudi.
  • 3.3. The acid endoprotease is specific towards haemoglobin and practically has no action on bovine serum albumin.
  • 4.4. In mouse normal red blood cells we find an acid protease having physico-chemical properties similar to the enzyme present in B. hylomysci extracts.
  • 5.5. The similarity of electrophoretic velocity between acid protease in B. hylomysci and non-infected red blood cells leads us to think that the acid protease of parasitic extracts comes from the host-cell.
  • 6.6. The proteolytic system of Babesia and Plasmodium are similar.
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12.
  • 1.1. Comparative studies of EGF, TGF-α, and TGF-βl action on the synthesis of DNA and cellular proteins in rat L6 myogenic cells and fetal bovine myoblasts demonstrated considerable differences between particular growth factors, dependent on dose and target cells.
  • 2.2. Among examined growth factors only EGF exerted mitostimulatory action, more pronounced at lower concentrations. EGF, progressively with dose, stimulated protein synthesis much more effectively in fetal bovine myoblasts than in L6 cells.
  • 3.3. The dynamics of stimulation of protein synthesis by TGF-α was greater than by EGF in both examined types of cell cultures.
  • 4.4. The maximal response of fetal bovine myoblasts to TGF-α in a concentration of 100 ng/ml reached 370%, whereas EGF in a 10 times higher concentration stimulated protein synthesis only to 123% of control.
  • 5.5. In contrast to EGF, TGF-α significantly inhibits DNA synthesis. Inhibition of the mitogenic response with simultaneous stimulation of protein synthesis by TGF-α may indicate changes toward cell differentiation.
  • 6.6. TGF-β 1 in smallest concentration inhibits both DNA and protein synthesis. The suppressive action of TGF-β 1 was more distinct in fetal bovine myoblasts than in the L6 cell line.
  • 7.7. Increasing concentrations of TGF-β l diminished its inhibitory effect, even leading to stimulation of protein synthesis at higher doses in L6 myoblasts.
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13.
  • 1.1. Nephron segments (rabbit) were dissected and explanted into primary culture.
  • 2.2. Outgrowth of epithelial cells and proliferation in monolayer from distal nephron segments was dependent upon cell substratum (plasma or collagen) and upon hormonal supplements of serum-free media.
  • 3.3. Distal nephron segments from cortex and outer medulla (thick ascending loop of Henle, collecting tubule) have differential requirements for growth-stimulation.
  • 4.4. Proximal epithelial tissue (embryonic Nephron Anlage) depends on serum or embryo extract for differentiation into convoluted segments.
  • 5.5. The mammalian nephron can be cultivated in vitro to form segmental epithelial monolayers.
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14.
  • 1.1. Inorganic phosphate (Pi) was absorbed rapidly by suspension-cultured cells of Catharanthus roseus which had previously been cultured in Pi-free Murashige Skoog medium.
  • 2.2. The intracellular levels of ATP, ADP and 5-phosphoribosyl-l-pyrophosphate (PRPP) increased markedly during the 24 hr which followed the addition of Pi (1.25mM).
  • 3.3. Availability of PRPP in vivo, estimated by the measurement of nucleotide synthesis from [8-14C]adenine, was also increased by addition of Pi.
  • 4.4. Only a 20% increase in the maximum catalytic activity of PRPP synthetase was observed in extracts of cells, prepared 24 hr after addition of Pi.
  • 5.5. In contrast to results for mammalian PRPP synthetase, the activity of PRPP synthetase, partially purified from Catharanthus roseus, was inhibited by concentration of Pi greater than 5mM.
  • 6.6. The mechanisms involved in the increased availability of PRPP and the synthesis of adenine nucleotides in the plant cells cultured in Pi-containing medium are discussed.
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15.
  • 1.1. Exposure of isolated Aplysia eyes to serotonin (10−7 M) produces large and long-lasting (hours) increases in the ERG recorded from the surface of the eye.
  • 2.2. Dopamine, octopamine, or acetylcholine do not mimic the effect of 5-HT on the ERG.
  • 3.3. Brief electrical optic nerve stimulation (2 Hz, 2 min) also increases the ERG and this effect also lasts a long period of time (0.5–2 hr).
  • 4.4. Our results suggest that serotonin increases the response of photoreceptor cells to light and that efferent optic nerve activity may modulate photosensitivity through release of serotonin in the eye.
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16.
  • 1.1. A potentiometric method for the assay of cholinesterase has been proposed and compared with a colorimetric assay.
  • 2.2. Main kinetic parameters of cholinesterase from Hypostomus punctatus brain were determined indicating that true acetylcholinesterase is by far the predominant enzyme in the brain of this fish.
  • 3.3. We have compared our data with published results described from other fish species.
  • 4.4. The enzyme inhibition achieved after 3 hr incubation of brain homogenates with ethyl-parathion have indicated that this enzyme shows a characteristic organophosphorous sensitive behavior.
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17.
  • 1.1. The intestinal absorption of insulin in carps was assessed examining the transepithelial passage of ingested gold-labeled hormone by electron microscopy. Insulin transfer occurred mainly through the intercellular spaces between the enterocytes.
  • 2.2. When reaching the lamina propria, the gold-labeled hormone gathered predominantly around the granules of the granular cells, and therefore can enter the circulatory system via the blood capillaries which are found in close contact with these cells.
  • 3.3. Winter-acclimatized carp were also capable of internalizing the hormone when fed with insulin.
  • 4.4. Furthermore, the absorbed hormone revealed full activity in regard to the observed changes in the ultrastructure of the liver cells of the treated cold-adapted fish.
  • 5.5. The fish ingesting the hormone underwent the same type of hepatic ultrastructure reprogramming observed when winter-acclimatized carps are injected intraperitoneally with insulin, i.e. conversion to a phenotype corresponding to hepatocytes from summer-adapted carp.
  • 6.6. The oral absorption of insulin by winter-acclimatized fish and its effect in reversing the cold-adaptive state might be useful for the fish culturing industry.
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18.
  • 1.1. Isolated photophores of the living bathypelagic fish Myctophum punctatum respond to train of weak (10–25 V) and short (2–5 msec) electrical stimuli applied at different frequencies (8–100/sec) by a luminus response.
  • 2.2. This response is characterized by a short emission latency time, the peak of light develops within about 2 sec after the beginning of the electrical stimulation: afterwards the light decreases to a constant level within about 8 sec.
  • 3.3. Stimuli of higher strength (60–75 V) and longer duration (8–16 msec) applied at different rates (1–100/sec) evoke brief flashes.
  • 4.4. The isolated supracaudal gland emits flashes in response to electrical stimulation whatever the strength and the duration of stimuli.
  • 5.5. The flash of the supracaudal gland differs from the flash of the isolated photophores in three respects: lower threshold, higher magnitude and longer duration.
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19.
  • 1.1. The Root effect was evaluated in hemolysates from 26 species of bony fish and 20 species of cartilaginous fish found on the Brazilian southeastern coast.
  • 2.2. Teleost Root shifts, with a single exception, are correlated with the presence of the choroid rete mirabile but not with its counterpart in the swimbladder.
  • 3.3. Five ray species displayed weak and moderate Root effects despite the absence of choroid and swimbladder rete.
  • 4.4. The presence and intensity of the Root effect is probably primarily related to the high oxygen demand of the retina and with the importance of visual perception in fish.
  • 5.5. In marine teleosts the magnitude of the Root effect seems to be associated with the presence and size of both the choroid rete and the pseudobranch.
  • 6.6. An antioxidant protection of the fish eyes can be advocated for the pseudobranch.
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20.
  • 1.1. A comparative study of the proteolytic activity in four different sections of the digestive tracts of the European sea bass (Dicentrarchus labrax) and hybrid striped bass (Morone chrysops × M. saxatilis) reared in freshwater revealed minor differences between these fish.
  • 2.2. Tryptic activity plays a major role in the proteolytic process in both fish.
  • 3.3. The activity of seven intestinal proteolytic enzymes was detected utilizing a combination of specific substrates and inhibitors.
  • 4.4. High levels of proteolytic activity were detected in both the proximal and distal sections of the fish intestine at a high pH range (9–10).
  • 5.5. In situ monitoring of pH levels revealed a lower pH level in the intestinal proximal section of hybrid striped bass compared with the distal section.
  • 6.6. In contrast, higher pH levels were detected at the proximal compared with the distal sections of D. labrax intestine.
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