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1.
  • 1.1. Blood volume and plasma biochemical changes and feed and water consumption in response to a hemorrhage by phlebotomy of 30% of the calculated total blood volume with and without replacement of blood volume with physiological saline were determined in juvenile male Coturnix coturnix japonica.
  • 2.2. Plasma protein and osmolality decreased rapidly posthemorrhage and did not recover by 72 hr posthemorrhage.
  • 3.3. Plasma glucose, Na+ and K+ increased within Ihr postphlebotomy. Plasma Na+ returned to nonphlebotomized levels within 6 hr postphlebotomy.
  • 4.4. Saline replacement of blood volume resulted in hypervolemia within 3–5 min postphlebotomy.
  • 5.5. Phlebotomized quail receiving no saline recovered blood volume to 0 hr (nonphlebotomized) levels within l hr postphlebotomy.
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2.
  • 1.1. The effect of acclimation to 10° and 30°C on the blood volume, clotting time, total blood protein and numbers of cells was determined in Uca pugilator.
  • 2.2. There was no significant difference between blood volume in the 10° and 30° animals but there were significantly more cells and a higher blood protein in the 30° crabs.
  • 3.3. The clotting time is significantly longer for the 10° crabs.
  • 4.4. These changes associated with the blood parameters can be associated with the ecology of the animal.
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3.
  • 1.1. The degree of rat erythrocyte lysis and immobilization of Trypanosoma brucei in infected blood by buffered hypotonie solutions of sodium chloride and sucrose was studied.
  • 2.2. At 0.3% sodium chloride solution 98% hemolysis of erythrocytes was achieved while 95% of the original bloodstream trypomastigotes survived and were found to be motile and viable for biochemical study.
  • 3.3. Further increase in the concentration of sodium chloride above 0.3% revealed an increase in the immobilization of trypanosomes and a decrease in the erythocyte hemolysis.
  • 4.4. Bloodstream trypomastigotes have been prepared by differential osmotic lysis of infected blood in 0.3% sodium chloride solution and used for studying their metabolism.
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4.
  • 1.1. Seasonal changes of circulating blood parameters of Natrix n. natrix were evident and involved both sexes to the same extent.
  • 2.2. A significant decrease in red cell count, haematocrit and haemaglobin concentration in the mating period, and an increase in those parameters and mean cell volume in autumn were observed, and haemodilution during winter torpor.
  • 3.3. The changes during the breeding season had probably a hormonal background; in winter, they resulted first of all from a decreased erythropoietic activity and, to a lesser extent, from an increased red blood cell breakdown rate. However, the possibility that some erythrocytes were withdrawn from the circulation cannot be excluded.
  • 4.4. Winter lymphocytopenia, eosinocytopenia and neutrophilic granulocytosis in females during egg laying were expressions of changes of leucocyte formula.
  • 5.5. Seasonal cyclicity was found only with respect to the white cell count in males and the eosinophile fraction in males and females.
  • 6.6. Probable reasons for, and mechanisms of the changes in blood composition are discussed.
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5.
  • 1.1. Some aspects of the gas exchange system of a diving lizard, Physignathus lesuewii were studied.
  • 2.2. Breathing patterns were analysed.
  • 3.3. Breathing rate increases logarithmically with temperature and Q10 = 1.8. LogBR = −0.237 + 0.0256 T.
  • 4.4. Gas tensions in lung air and arterial and venous blood were measured. Arterial pH declines with increasing temperature.
  • 5.5. Temperature has a marked effect on oxygen affinity of the blood (ΔH = −10.1 kcal mol). A Bohr effect was also noted.
  • 6.6. CO2 equilibrium curves were drawn.
  • 7.7. The results are considered with a view to anticipating the efficiency of the gas exchange system of this species under conditions of variable temperature and during diving.
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6.
  • 1.1. Phascolopsis gouldi, the commonly studied sipunculan of the Woods Hole area, Massachusetts, can tolerate a salinity range from about 45% seawater to at least 100% SW, with literature records extending to about 160% SW. There was no survival at 40% SW.
  • 2.2. Over this salinity range, P. gouldi is an osmotic and ionic conformer.
  • 3.3. The osmotic and sodium concentrations of the coelomic fluid are the same as that of the medium; the chloride concentration is about 9% less than that of the medium; the potassium concentration is about 30% higher.
  • 4.4. Analysis of water content regulation by two different approaches shows that P. gouldi does have a limited ability for volume regulation, restricted to salinities higher than 58% SW.
  • 5.5. P. gouldi is not a “simple osmometer”.
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7.
  • 1.1. Dogfish (Squalus acanthias) were acclimated to reduced salinities and their plasma, muscle tissue and erythrocytes subsequently analysed.
  • 2.2. Decrease in the osmolarity of the plasma was principally due to a fall in urea concentration and a significant fall in the concentrations of sodium and chloride.
  • 3.3. Changes in the muscle and erythrocytes in dilute media were a decrease in urea, potassium, sodium and chloride concentrations.
  • 4.4. The concentrations of the free amino acids in the muscle and the red blood cells decreased more than would be expected by the movements of water only.
  • 5.5. The results were discussed in relation to the regulation of cellular volume and the involvement of the free amino acid pool of the tissues in this process.
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8.
  • 1.1. We studied the morphology and contractile properties in marginal sphincters isolated from anemones from different environments.
  • 2.2. Sphincters from specimens from protected areas are ovoid or roughly square shape. Oval sphincters have increased number of mesogloeal branches and the main axis is thickened. Roughly square sphincters have irregular borders, mesogloeal axes of uniform thickness and homogeneous branching.
  • 3.3. Specimens from exposed areas have sphincters with an ovoid shape and dichotomous branching.
  • 4.4. Sphincters of specimens from partially protected areas show transition forms.
  • 5.5. Under stimulation with KCl at different concentrations, sphincters of anemones from exposed environments contract faster and develop higher isometric forces than muscles isolated from specimens of protected areas.
  • 6.6. It was concluded that sphincters of anemones from different environments have a morphology and a physiological response adapted to the milieu.
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9.
  • 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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10.
  • 1.1. The ventricle cells of the flounder (Platichthys flesus) maintained the cell volume regulation mechanism in vitro, when isolated hearts were submitted to a hyposmotic solution.
  • 2.2. The initial osmotic swelling of the cells was followed by a secondary shrinking. A new steady state volume (water content) was established in the course of 6 hr. The water content was 3% above control.
  • 3.3. The cellular amount of K+ and taurine decreased concomitantly with the decline in cellular water.
  • 4.4. The decrement in cellular taurine was explained by leakage of taurine, per se, into the perfusion media.
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11.
  • 1.1. This study deals with the hematological and blood chemistry of 13 adult marsh harriers (Circus aeruginosus).
  • 2.2. No significant differences were observed between male and female groups in any of the parameters.
  • 3.3. The value of white blood cells was 14,677/mm3 heterophils and lymphocytes, these being the most abundant cellular type (81.42 and 12%, respectively).
  • 4.4. Urea and uric acid are present in approximately similar proportions, though birds are said to be uricotelic.
  • 5.5. The cholesterol concentration values determined in our study, are higher than those reported in most other birds.
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12.
  • 1.1. A choriolytic enzyme was isolated from the hatching medium of the pike, Esox lucius.
  • 2.2. The enzyme is defined as hatching enzyme.
  • 3.3. The molecular weight of the enzyme is 24,000.
  • 4.4. The enzyme is a glycoprotein containing 2% carbohydrate.
  • 5.5. Its isoelectric point is 6.5.
  • 6.6. The pH optimum is around pH 8.
  • 7.7. The enzyme molecule contains two disulfide bonds but no free cysteine.
  • 8.8. Inhibitor studies and metal analysis show that the enzyme is a zinc-metalloprotease.
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13.
  • 1.1. The utility of biochemical genetic methods of bird identification was investigated for some common species which create a hazard for commercial aviation in Ireland.
  • 2.2. Sixteen enzyme loci were assayed in eight species, using starch gel electrophoresis; three larids, three corvids and two columbids.
  • 3.3. Genera were distinguishable using all but two loci.
  • 4.4. Differences within genera were small, but all species except for the gulls Larus argentatus and L. marinus, could be identified using one or more loci.
  • 5.5. Arising from the success of the method using fresh specimens, a protocol for the electrophoretic identification of traumatized remains of strikes is suggested.
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14.
  • 1.1. Cells of tentacles and body wall of the sea anemone Condylactis gigantea behaved as simple osmometers during 5hr exposure to 50, 67, 83, 100 and 125% sea-water.
  • 2.2. All intracellular water appeared to be osmotically active.
  • 3.3. Cell sodium, chloride and total osmolyte content remained invariable, with taurine decreasing and potassium increasing as sea-water concentration was reduced.
  • 4.4. Tissues, as a whole, exhibited a pseudoregulatory response to changes in salinity as the large and osmotically inert extracellular space buffered volume changes to a considerable extent.
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15.
  • 1.1. Kinetic aspects of the enzyme UDP-galactose 4-epimerase in crude homogenates of the albumen gland of the snail Lymnae stagnalis were estimated. The mean values of the Km for UDP-galactose and for NAD are 0.343 and 0.097 mM, respectively. The enzyme is inhibited by NADH. It is inactivated by freezing and raised temperature (25°C), but it can be reactivated by NAD.
  • 2.2. In the albumen gland the epimerase activity is 10–100 times higher than in other tissues, reflecting the high turnover of glucose to galactose, essential for the synthesis of galactogen in this organ.
  • 3.3. In fed snails long day conditions stimulates albumen gland epimerase activity, coinciding with high egg production.
  • 4.4. In starved snails a fairly high residual activity of the enzyme is maintained, irrespective of photoperiod or egg production.
  • 5.5. Trematode infection leads to a considerable reduction of the epimerase activity.
  • 6.6. The results indicate that the epimerase activity in fed snails, when the gland shows a regular release, reflects long-term adaptations (photoperiod). In starved and parasitized snails, when no regular release or product occurs, a basic epimerase activity is maintained. This might be important for a rapid restoration of egg production after the termination of adverse conditions.
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16.
  • 1.1. Oxygen equilibrium curves were measured on trout red blood cell suspensions at pH 7.8 and 8.4 at 15, 20 and 25 C. Normal red cells and red cells that had been depleted of their ATP content were used.
  • 2.2. The equilibrium data were fitted to the Adair's model and the enthalpy (ΔH) and entropy (ΔS) changes for the first and fourth steps of oxygenation and for overall oxygenation were calculated from the temperature dependencies of the Adair constants.
  • 3.3. For normal red blood cells, the apparent heat for the first oxygenation step, δh1, is close to zero.
  • 4.4. Temperature insensitivity of this step at physiological pH, combined with a large pH dependence, probably denotes a property of Hb4, the Root effect Hb of trout blood.
  • 5.5. At pH 7.8, ΔH4 is about —4kcal/mol, a small value which may be attributed to the large release of Bohr protons that occurs at the last oxygenation step and corresponds to an endothermic process which opposes to the exothermic oxygenation of the haem.
  • 6.6. The ΔH4 value appears to have a large influence on the enthalpy for overall oxygenation.
  • 7.7. Results for ATP-free red cells are consistent with a mere increase in the intracellular pH and suggest that ATP has no specific effect at and above pHi ~ 7.7.
  • 8.8. Effects of temperature and pH on trout red blood cell isotherms emphasize the primary importance of the major component of trout blood, namely Hb4, in trout blood functional properties.
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17.
  • 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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18.
  • 1.1. The effect of fetal calf serum as an additive for reconstituted freeze-dried bovine and porcine blood for feeding Glossina palpalis palpalis was determined.
  • 2.2. Reproductive performance of tsetse flies fed reconstituted freeze-dried bovine and porcine blood supplemented with fetal calf serum was higher than that of flies fed only freeze-dried blood.
  • 3.3. Sonicated freeze-dried porcine blood supplemented with fetal calf serum resulted in a reproductive performance equivalent to that of flies fed on non-sonicated freeze-dried porcine blood and fetal calf serum.
  • 4.4. A 50:50 mixture of freeze-dried porcine and freeze-dried bovine blood reconstituted and sonieated resulted in a reproductive performance equivalent to the highest ever attained for in vitro-reared G.p. palpalis.
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19.
  • 1.1. When blood flows, membranes are bombarded with ions etc., whose entry creates an ATP demand proportional to flow rate. Also proportional to flow rate is ATP production from oxidation of substrates [S] from the same blood volume.
  • 2.2. O2 is limiting and reaction velocity at rest (metabolic rate) is determined by flow rate, F, but not by [S].
  • 3.3. Since resting blood O2 A-V difference is about 5 vol%, 11 circulated produces about 0.25 kcal in mammals, birds or warm reptiles.
  • 4.4. Where O2 is not limiting, as in most amino acid deaminations, V = K F[S] with K a constant unrelated to Km.
  • 5.5. At equal blood vol/kg, solid geometry dictates that the average cross-sectional area of major vessels/kg will be an inverse function of body mass. The smaller the animal, the shorter the vessels, the “thicker” the vessels/kg body wt, and at any one blood pressure, the higher the flow/kg/hr. If a man's major vessels were equal in cross-section/kg to those of a shrew, it would take 2241 of blood to fill them.
  • 6.6. Growth decreases flow/kg (and therefore metabolic rate), by decreasing vessel cross-section/kg without changing blood pressure or linear velocity of flow.
  • 7.7. Surface area/g, body wt to some power, average vessel length/kg, circulation time and average major vessel cross-sectional area are all related mathematically.
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20.
  • 1.1. Using laser Doppler techniques in man, we have previously demonstrated differences in skin blood flow properties at sites with primarily nutritive (NUTR) perfusion, such as the elbow or knee, as compared to sites such as the finger pulp, with predominantly arteriovenous anastomotic (AVA) perfusion.
  • 2.2. Basal and heat stimulated flow is greater at AVA sites. In man, blood pressure changes are reflected primarily by changes at AVA rather than NUTR sites.
  • 3.3. These blood pressure induced changes affect the red blood cell velocity (VEL) component at AVA sites more than microvascular volume (VOL).
  • 4.4. Given these findings in man, we decided to compare skin blood flow properties in a suitable animal model.
  • 5.5. We chose the Wistar-Kyoto (WKY) and Spontaneously Hypertensive Rat (SHR) strains, in view of the marked difference in systemic blood pressure in these two related strains.
  • 6.6. Skin blood flow varied considerably at different skin sites in the rats. Skin sites with hair covering, on the back and at the base of the tail, showed low basal and heat stimulated blood flow.
  • 7.7. In contrast, the plantar surface of the paw behaved similarly to the finger or toe pulps in man, with 3–4-fold higher basal flow than the hair covered areas and a 7–8-fold rise with local heating to 44°C.
  • 8.8. Furthermore, there was a 25% greater blood flow at the plantar paw surface in the SHR rats as compared to the WKY rats, corresponding to the 25% higher systemic blood pressure in these animals.
  • 9.9. The heat induced increase in flow at the plantar surface of the paw was primarily a result of a marked increase in VEL rather than VOL.
  • 10.10. The higher flow at this site in SHR as compared to WKY rats was likewise ascribable to an increase in VEL, VOL being equivalent in the two strains.
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