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1.
  • 1.1. A monomeric myoglobin is present in the muscles of the proboscis of the polychaete Glycera dibranchiata. This myoglobin differs in structure and function from the monomeric hemoglobin found in this animal's coelomic cells.
  • 2.2. The myoglobin has a very high oxygen affinity and a high carbonmonoxide combination rate. The high oxygen affinity of this myoglobin is well suited physiologically to supply oxygen to muscles of the proboscis which are used in burrowing and feeding.
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2.
  • 1.1. A 12 week program of treadmill exercise (0.7 m/sec, 30 min per day, five days per week), significantly increased the myoglobin concentration of the femorotibialis medius muscle in bar-headed geese as compared to nonexercised controls.
  • 2.2. The myoglobin concentration differed among various muscles within a bird. The highest myoglobin concentrations were found in the primary flight muscle, the pectoralis major, and in cardiac muscle.
  • 3.3. By physically conditioning their muscles, bar-headed geese may improve the oxygen flow to mitochondria and, thereby, enhance their ability to exercise under conditions of low oxygen partial pressures.
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3.
  • 1.1. Myoglobins from heart and skeletal muscle of turtles were analyzed by thin-layer isoelectric focusing.
  • 2.2. Within the subfamily Emydinae, variation in the occurrence of two myoglobin electromorphs (pI 6.8 and 6.9) was detected.
  • 3.3. Patterns of myoglobin polymorphism support dividing the Emydinae into two subfamilies and help resolve controversial theories on relationships of the genus Deirochelys.
  • 4.4. Possible adaptive significance of the myoglobin variants (isoforms) remains to be determined.
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4.
  • 1.1. The effects of niacin deficiency on the relative turnover rates of proteins in various tissues of Japanese quail were investigated.
  • 2.2. The level of liver NAD was not affected by niacin deficiency whereas the level of pectoral muscle NAD was markedly reduced.
  • 3.3. In all dietary treatments the liver had the highest turnover rates of proteins, heart and brain had intermediate rates, and pectoral muscle had the lowest rates.
  • 4.4. Relative turnover rates of proteins in all tissues (particularly pectoral muscle) of the niacin deficient group were significantly higher than those of pair-fed control group, although there were no significant differences in turnover rate between pair-fed control and control groups.
  • 5.5. The high turnover rate of proteins in niacin deficiency was primarily attributed to enhanced degradation rate of proteins rather than enhanced synthesis rate of proteins.
  • 6.6. Optical density scanning (or densitometric) of water-soluble pectoral muscle proteins separated by isoelectric focusing revealed several additional minor protein bands between major protein bands in the niacin deficient group which were more pronounced in the acidic region of the gel.
  • 7.7. These results suggest that proteins with a low pI value in pectoral muscle of the niacin deficient animal are highly sensitive to protein degradation.
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5.
  • 1.1. Patterns of fuel utilization in the thoracic muscles of three species of ants have been established.
  • 2.2. The thoracic muscles of Formica ulkei exhibit a typical Hymenopteran metabolic organization, relying exclusively upon carbohydrate oxidation for the provision of metabolic energy. This species feeds upon honeydew.
  • 3.3. Pogonomyrmex californicus, a granivorous ant, exhibits a metabolic organization unprecedented for a Hymenopteran species. Its thoracic energy metabolism is based upon lipid oxidation.
  • 4.4. Atta colombica, a fungus feeder, can metabolize both carbohydrate and fat, a versatility which is not typical of Hymenoptera.
  • 5.5. It is concluded that patterns of fuel utilization in insects are not determined by phylogenetic inertia, but are selected to accommodate the activity patterns, feeding ecology and dietary regime of the species.
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6.
  • 1.1. Intracellular pH buffering capacity of hagfish (Eplatretus cirrhatus) dental plate retractor muscles is among the highest reported for any vertebrate muscle.
  • 2.2. Over 80% of the pH buffering capacity of hagfish retractor and myotome muscle is due to components other than proteins and phosphate.
  • 3.3. The muscles have less than 0.5 μmol/g wet weight of l-histidine, and lack l-l-methyl histidine, l-3-methyl histidine and the histidine-containing dipeptides anserine, carnosine and ophidine.
  • 4.4. Instead, they contain an unidentified low molecular weight acid-soluble compound to which the high pH buffering capacity can be attributed.
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7.
  • 1.1. Glucose entry rate was measured in two camels (Camelus dromedarius) and two sheep (Ovis wies) in the fed state and also after 72 hr of fasting.
  • 2.2. Plasma glucose concentration in the fed camels (129 mg/100 ml) was considerably higher than that of the fed sheep (63 mg/100 ml).
  • 3.3. The mean glucose entry rate in the fed camels (1.67mg/min per kg body wt) was very similar to the sheep (1.79 mg/min per kg body wt).
  • 4.4. When the results were expressed as a function of the metabolic body size, the entry rates in the camel were 1.5 times greater than that of the sheep.
  • 5.5. The relationship between glucose entry rate and plasma glucose concentration in different mammalian species is discussed.
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8.
  • 1.1. The organic composition of the body tissues of eight species of deep-sea aspidochirotid holothurian, collected between 500 and 4100m depth in the NE Atlantic Ocean, was obtained by the biochemical analysis of protein, lipid, carbohydrate and % ash.
  • 2.2. The major organic class was protein with soluble lipid the major soluble fraction in the ovary. Carbohydrate values were consistently low.
  • 3.3. The calorific value was significantly higher in the ovary than in the other tissues.
  • 4.4. The total body calorific content for two selected species, Benthothuria funebris and Mesothuria lactea, was 25.62 and 26.24J/mg ash-free dry weight (AFDW).
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9.
  • 1.1. The mechanism of action of glyburide (a sulfonylurea) on muscle has been investigated by measuring glucose uptake and glucose transporter (GLUT4) protein levels after chronic glyburide treatment.
  • 2.2. A dietary induced insulin resistant rat model (4 wk of high-fat, high-sucrose feeding) was given glyburide (2mg/kg/day) for 10 days and glucose uptake was measured in a perfused hindquarter preparation.
  • 3.3. Protein levels of the GLUT4 glucose transporter were determined by Western analysis.
  • 4.4. After 7 days of treatment, rats fed glyburide had lower blood glucose concentrations 2 hr (72 ± 5 vs 103 ± 12 mg/dl) and 24 hr (97 ± 7 vs 123 ± 7 mg/dl) after glyburide administration with no difference in serum insulin levels compared to vehicle treated animals.
  • 5.5. Glucose uptake was approx doubled in basal state (0 insulin) in response to glyburide (2.8 + 0.4 vs 1.7 ± 0.2μ mol/g per hr).
  • 6.6. Maximal insulin (100 nM) stimulated glucose uptake tended to be higher in the glyburide treated group, but did not reach statistical significance (8.0 ± 0.7 vs 7.0 ± 0.6 μmol/g per hr).
  • 7.7. Western analysis revealed no significant effect of glyburide on the GLUT4 protein level in skeletal muscle.
  • 8.8. These results suggest that glyburide alters glucose uptake through some mechanism other than alterations in the level of the GLUT4 glucose transporter protein.
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10.
  • 1.1. Lactic dehydrogenase dehydrogenase isozymes and other respiratory enzymes were studied in degenerating intersegmental muscles of Manduca sexta and Antheraea polyphemus.
  • 2.2. Total activities of the different enzymes (isocitric dehydrogenase, malic dehydrogenase, catalase, lactic dehydrogenase) decline at varying rates, starting before the rapid phase of involution.
  • 3.3. One isozyme of LDH, an M-type isozyme, increases several-fold during the final three days prior to the emergence of the insect.
  • 4.4. The same isozyme appears very transiently or not at all in muscles which do not break down, and is present in degenerating silk glands at the time of their most rapid involution.
  • 5.5. The data suggest that limitation of oxidative metabolism plays a role in the involution of the muscles.
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11.
  • 1.1. A novel glycogen phosphorylase inhibitor was partially purified from crayfish hepatopancreas.
  • 2.2. The inhibitor was found only in two species of crayfish examined, and not in lobster, fresh and salt water clams, mussels or cockroaches.
  • 3.3. The inhibitor is a small protein (Mr = 23,000) which did not show proteolytic activity.
  • 4.4. Preliminary kinetic analysis of the inhibitory mechanism indicated that it bound to both glycogen and the glycogen phosphorylase protein.
  • 5.5. Inhibitor binding to glycogen resulted in a competitive inhibition pattern with respect to glycogen phosphorylase (inhibition constant of ca 10 μg/ml).
  • 6.6. The inhibitor also bound glycogen phosphorylase directly with a binding coefficient of 100 μg/ml resulting in a partially non-competitive inhibition pattern with respect to phosphate.
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12.
  • 1.1. In a continuing investigation of phycocyanin-membrane surface interaction, fluorescence quenching experiments were performed with a mixture of two populations of fluorescence probe-encapsulated phospholipid bilayer vesicles in the presence and absence of phycocyanin.
  • 2.2. These membrane vesicles were prepared with 1,2-dimyristoyl phosphatidylcholine (DMPC), cholesterol and a probe molecule.
  • 3.3. A fluorophore was encapsulated in one population of membrane vesicles, while a quencher was encapsulated in another population of membrane vesicles.
  • 4.4. The result was compared with those of experiments in the presence of other biomolecules, including albumin, cytochrome c, hemoglobin, myoglobin or RNA.
  • 5.5. Interestingly, a one-third reduction of the fluorescence intensity was observed in the mixture of these two populations of membrane vesicles in phycocyanin's presence.
  • 6.6. In contrast, the other biomolecules caused no significant reduction in the fluorescence intensity.
  • 7.7. These findings were evidence of a phycocyanin-induced membrane perturbation.
  • 8.8. This was further demonstrated by a phycocyanin-induced change in the thermotropic behavior of DMPC vesicles, as measured by differential scanning microcalorimetry.
  • 9.9. Such a unique property of phycocyanin is believed to be associated with its known membrane surface-interacting character.
  • 10.10. A possible phycocyanin-modulated membrane-membrane interaction was discussed.
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13.
  • 1.1. The composition of bile pigments in the blood and bile of 39 species were studied.
  • 2.2. Conjugated bilirubin (trace to 4.62 mg/100 ml) was detected in the serum of most fish, while biliverdin (trace to 2.0 mg/100ml) was detected only in Anguilla Japonica, Thalassoma lunare and Clinocottus analis.
  • 3.3. Analysis showed tht there are two types of bile pigments excretion pattern in these fishes. The first pattern excretes bilirubin (most conjugate) predominantly, the other excretes mostly biliverdin with some bilirubin. However, during starvation, the excretion of conjugate bilirubin gradually shifted to unconjugated biliverdin. The rate of shifting varies with species.
  • 4.4. Introduction of bilirubin into Anguilla japonica produced an initial excretion of mono-conjugates, followed by di-conjugates. Introduction of biliverdin caused an increased in the excretion of unconjugated biliverdin, but no significant increase of bilirubin in the bile was detected.
  • 5.5. A binary excretion pathway of bile pigments in fish is proposed. The evolutionary characteristics of heme catabolism in terrestrial animals with respect to this pathway is discussed.
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14.
  • 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
  • 2.2. The O2 in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O2 concentration down to 1.6 mg/l.
  • 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q10) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
  • 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.
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15.
  • 1.1. Small quantities of sea water were recyclically perfused over the surface of paired anterior byssus retractor muscles of Mytilus californianus.
  • 2.2. Dopamine was identified in the perfusate by thin-layer chromatography.
  • 3.3. Stimulation of the pedal ganglion caused the dopamine content of the perfusate to increase.
  • 4.4. A significant increment of release of dopamine was detected at stimulation frequencies above 3 Hz and increased progressively with increase in stimulation frequency.
  • 5.5. The possibility of a role for dopamine as a relaxing or inhibitory neurotransmitter in Mytilus is considered in relation to the present and related evidence and to the actions of 5-HT, the probable relaxing transmitter.
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16.
  • 1.1. The role ofinterleukin-1 (IL-1) in sepsis-induced muscle proteolysis was assessed by treating septic rats with recombinant IL-1 receptor antagonist (rIL-Ira).
  • 2.2. In initial experiments, we tested the effectiveness of IL-Ira in preventing muscle proteolysis induced by administration of IL-1.
  • 3.3. When normal rats were treated with rIL-α (three intraperitoneal doses of 100 μ g/kg body weight each over 16 hr), total and myofibrillar muscle protein breakdown rates, measured as release oftyrosine and 3-methylhistidine, respectively, by incubated extensor digitorum longus muscles, were significantly increased.
  • 4.4. This metabolic response to IL-α was completely abolished by rIL-Ira, administered as three intraperitoneal doses of 3 mg/kg body weight each over 16hr.
  • 5.5. In subsequent experiments, sepsis was induced in rats by cecal ligation and puncture (CLP); non-septic rats were sham-operated.
  • 6.6. Treatment of septic rats over 16hr with a total dose of 25mg/kg body weight of rIL-Ira reduced, but did not normalize, the increased muscle protein breakdown rates seen during sepsis.
  • 7.7. When the dose of rIL-Ira was more than doubled and given as a constant infusion at a rate of 4.2 mg/kg body weight/hr for 16 hr, the increased rate of muscle proteolysis in septic rats was normalized.
  • 8.8. The present study offers the first direct evidence that IL-1 is involved in the regulation of muscle proteolysis during sepsis.
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17.
  • 1.Total lipids, free fatty acids, triglycerides, phospholipids and total cholesterol in blood serum, liver, brain, cardiac and skeletal muscles of Naja haje haje were determined during the different phases of the hibernation cycle.
  • 2.A sharp decrease in the level of total lipids of blood serum and all tissues occurred during hibernation. Upon arousal, lipogenesis is commonly restored.
  • 3.Elevated concentrations of serum free fatty acids predominated in pre-hibernation and hibernation periods, while the tissues recorded highly significant declines during hibernation.
  • 4.Occurrence of marked decreases in triglycerides contents of serum and tissues except the cardiac muscles in the hibernation and arousal phases.
  • 5.Sharp increases in the phospholipid contents of blood and the selected tissues were recorded during hibernation. The level declined in both liver and cardiac muscles in arousing animals.
  • 6.Total cholesterol level was lowered in blood during hibernation. The cardiac muscles showed a highly significant decrease while liver, brain and skeletal muscles showed elevations in the same phase.
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18.
  • 1.1. The pathway and distribution of motor neurons in the uropod muscles of the crayfish, Procambarus clarkii, was investigated electrophysiologically and histologically.
  • 2.2. There were three crossing points of motor neurons between the peripheral motor bundle originating from the second and third roots of the sixth abdominal ganglion.
  • 3.3. It seems that there are no anatomical and functional regularity in the innervation pattern of the uropod muscles.
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19.
  • 1.1. The concentration of protein in the haemolymph of Balanus hameri ranged from 2.0 to 17.3 mg/ml, and the lipid from 1.4 to 7.7 mg/ml; the haemolymph protein and lipid levels increased significantly prior to cross-fertilization.
  • 2.2. The protein and lipid concentrations in Balanus balanus haemolymph were 8.1 and 1.7 mg/ml respectively.
  • 3.3. The lipid concentration of Lepas anatifera haemolymph was 1.2 mg/ml.
  • 4.4. The neutral lipid and phospholipid components of B. hameri and L. anatifera haemolymph were the same, with the major components of the phospholipid fraction being phosphatidyl ethanolamine and phosphatidyl choline.
  • 5.5. The osmolarity (970.4 mOsm), chloride ion concentration (501.3 m-eq/l) and pH (7.29) of B. hameri haemolymph were also determined.
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20.
  • 1.1. The fiber types of uropod muscles of the crayfish, Procambarus clarkii, were determined by the myofibrillar ATP-ase histochemistry and electrophysiology.
  • 2.2. The ATP-ase histochemistry was carried out on the sections of the whole tailfan and the slow muscles were identified as being of the slow type on the basis of their low staining intensities.
  • 3.3. The location of slow bundles in the mixed type muscles i.e. the dorsal rotator (DRT), the ventral rotator (VRT), and the telson-uropodalis posterior (TUP) was confirmed.
  • 4.4. TUP was newly revealed in this study to be a mixed muscle.
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