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1.
  • 1.1. Lipid changes occur in the developing tadpole of A. dacnicolor. The phosphatidylcholine content of liver and tail decrease during metamorphosis.
  • 2.2. In liver, the fatty acids of phosphatidylcholine and phosphatidylethanolamine become more unsaturated.
  • 3.3. In skin, phosphatidylcholine becomes more unsaturated and phosphatidylethanolamine becomes more saturated.
  • 4.4. In tail, phosphatidylcholine becomes more saturated and phosphatidylethanolamine shows no change.
  • 5.5. Triglycerides become more unsaturated in skin but become more saturated in tail.
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2.
  • 1.1. AMP deaminase from Palaemon serratus tail muscle was partially purified by chromatography on cellulose phosphate.
  • 2.2. Muscle homogenates expressed very low enzyme activities and the presence of ATP was necessary to detect AMP deaminase. The specific activity and substrate affinity of the purified enzyme were also very low.
  • 3.3. The purified prawn muscle AMP deaminase was contaminated by contractile proteins, one of the major contaminants being actin.
  • 4.4. The enzyme displayed a very high affinity for actomyosin which was only partially abolished by pyrophosphate.
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3.
  • 1.1. Cycloheximide and puromycin inhibited leucine transport and incorporation into isolated bullfrog tadpole tail and hepatic cells.
  • 2.2. However, high concentrations of these 2 inhibitors did not affect alanine incorporation appreciably in either tissue.
  • 3.3. NEM and DNP inhibited leucine and alanine incorporation in both cell types, but at different concentrations.
  • 4.4. NEM stimulated leucine transport only in hepatocytes; alanine transport was inhibited by NEM in tail fin cells.
  • 5.5. The results suggest different mechanisms of transport and protein synthesis for the 2 types of amino acids by tadpole liver and tail fin cells.
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4.
  • 1.1.The study was designed to determine if there are sex-dependent differences in vascular reactivity to adrenergic agents.
  • 2.2.Vascular reactivity of both aortic and tail artery smooth muscle from male and female rats to various vasoactive agents was assessed. 3.li]The vascular response of aortic smooth muscle to both phenylephrine and isoproterenol were significantly greater in male rats as compared to females.
  • 3.4.There were apparent sex differences in responsiveness to the KCl-induced, non-receptor mediated contraction of aortic smooth muscle in that the sensitivity to KCl was enhanced in male rats.
  • 4.5.No sex differences were observed in tail artery preparations.
  • 5.6.Phentolamine reduced the maximal tension induced by KCl in the tail artery but not aortic artery preparations. This effect was not sex dependent.
  • 6.7.No differences in the vascular smooth muscle responsiveness to acetylcholine or sodium nitrate was observed between groups or within different vascular beds.
  • 7.8.The increased sensitivity of males to adrenergic challenge could explain in part some of the existing sex differences in cardiovascular disease and hypertension.
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5.
  • 1.1. MFO enzyme activities were measured in microsomes from whole mussels (Mytilus galloprovincialis) comber livers (Serranus cabrilla), or Posidonia oceanica etiolated tissues, and PAH contents were determined in sediments collected in coastal locations of the French Riviera and Corsica during 3 oceanographic cruises in 1987–1988.
  • 2.2. BaP activities in mussel and EROD activities measured in fish were strongly correlated to the log of PAH content in sediments. The first results for CA4H in Posidonia showed significant differences related to PAH pollution levels. The increase in MFO activities measured in Corsica in summer 1988 indicated a recent petroleum contamination.
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6.
  • 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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7.
  • 1.1. An anatomical and physiological investigation was made of several components in the withdrawal escape response of the hermit crab, Pagurus pollicarus.
  • 2.2. In the fused last thoracic-first abdominal ganglion, the giant axon (GA) synapses with the giant motor (GM) neuron which innervates the abdominal flexor muscles.
  • 3.3. The synapse is unidirectional, conducting impulses only from the GA to the GM.
  • 4.4. The synaptic delay time is less than 0.4 msec.
  • 5.5. Concentrations of MgCl2 and MnCl2 which normally block chemical synapses were ineffective in interfering with GA-GM transmission.
  • 6.6. The GA-GM synapse was reversibly blocked by 0.5 mM DNP.
  • 7.7. It is concluded that GA-GM connection is a rectifying electrical synapse.
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8.
  • 1.1. The response to light of Hermissenda photoreceptors when recorded intracellularly without interference from synaptic and action potentials consisted of three phases: an early depolarization (ED) followed by hyperpolarization (dip) and subsequent depolarization (tail).
  • 2.2. The ED and the dip were associated with increased membrane conductance while decreased membrane conductance was involved with the tail.
  • 3.3. The dip reversal potential was − 82.1 ± 5.3 mV and its amplitude varied inversely with the log of [K+].
  • 4.4. Perfusing with agents which block K+ current like 4AP, Quinine, Quinidine or injection of TEA eliminated the dip and its associated increased membrane conductance, thus further supporting the role of K+ conductance in producing the dip.
  • 5.5. The dip was enhanced by increased [Ca2+]o, reduced by decreased [Ca2+]o and abolished together with its associated increased membrane conductance when perfused with either D600, Cd2+, Mg2+, Mn2+, or Co2+, which block transmembrane Ca2+ current.
  • 6.6. The dip and its associated increased membrane conductance were abolished by intracellular injection of EGTA and enhanced by perfusion with Ruthenium red.
  • 7.7. Intracellular injection of Ca2+ mimicked the dip: membrane conductance was increased and the cell hyperpolarized.
  • 8.8. These results indicate that the increase in intracellular [Ca2+] is primarily responsible for the light-induced increase of K+ conductance during the dip. The possible source of the Ca2+ is, at least in part, extracellular due to activation of an inward Ca2+ current.
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9.
  • 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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10.
  • 1.1. Studies characterizing glucose transport in the frog sartorius were performed.
  • 2.2. For nonstimulated and stimulated muscles, intracellular 2-deoxyglucose exceeded 2-deoxyglucose-6-phosphate at 15 min, showed little further increase, and was maintained below the extracellular concentration for 2 hr.
  • 3.3. Accumulated 2-deoxyglucose-6-phosphate did not inhibit glucose transport.
  • 4.4. Unlike in adipocytes, basal and stimulated 2-deoxyglucose transport showed no difference in sensitivity to N-carbobenzoxy-glycyl-l-phenylalaninamide.
  • 5.5. Phenylarsine oxide blocked contraction-enhanced 2-deoxyglucose uptake.
  • 6.6. These results suggest that the glucose transporter of the sartorius exhibits auto-regulation, and that basal transport is not regulated by the same process as in adipocytes.
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11.
  • 1.1. The effect of myo-inositol on the ability of three species of nematodes to survive desiccation has been studied.
  • 2.2. Survival rates obtained from worms treated with an inositol bathing medium were compared with survival rates of worms treated with distilled or tapwater media.
  • 3.3. Highest survival rates were found in those nematodes that were placed in an inositol solution prior to desiccation.
  • 4.4. Tapwater facilitated higher revival rates than did distilled water in both D. dipsaci and D. myceliophagous.
  • 5.5. No such differences were found for A. tritici.
  • 6.6. The results are discussed in relation to the possible mechanisms of protection afforded by the different bathing media.
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12.
  • 1.1. Seven natural populations of Dacus dorsalis were analyzed for a dimeric esterase by means of horizontal starch-gel electrophoresis.
  • 2.2. The electrophoretic phenotypes were governed by nine codominant Est-D alleles.
  • 3.3. The commonest allele in all seven population samples was Est-D100 which encoded an electrophoretic band with intermediate mobility.
  • 4.4. The distribution of EST-D phenotypes were in accordance with Hardy-Weinberg expectations.
  • 5.5. There was no geographic variation in the distribution of Est-D alleles.
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13.
  • 1.1. Seasonal variation in total lipids was examined in several body components of the turtle Sternotherus odoratus.
  • 2.2. Carcass fat stores in both sexes were depleted during winter. Additionally, a decline in carcass lipids was associated with increases in gonadal mass.
  • 3.3. Concentrations of liver lipids were maximal during August and minimal during winter.
  • 4.4. Males showed little seasonal change in plasma lipid levels, whereas females had seasonal peaks temporally associated with ovarian development and carcass fat storage.
  • 5.5. Ovarian concentrations of lipids were minimal after nesting and increased during fall.
  • 6.6. Results suggest that S. odoratus uses stored fats both for reproduction and maintenance during winter.
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14.
  • 1.1. Carp red cells were treated with drugs that affect the cell membranes. The water content of the cells and the accumulation of cAMP in the cells were measured in normoxia and in hypoxia using non-stimulated and adrenergically stimulated cells.
  • 2.2. WGA, DIDS + CCCP and A23187 increased the water content of nonstimulated normoxic cells.
  • 3.3. In hypoxia ouabain and DIDS + CCCP increased the water content but cytochalasin B, NPM, DIDS, CCCP and A23187 + CA2+ abolished the hypoxia-induced swelling.
  • 4.4. Any membrane perturbation induced some cAMP formation, Sophora and Anquilla lectins being most potent.
  • 5.5. Also in adrenergically stimulated cells, membrane perturbation generally increased cAMP formation.
  • 6.6. However, cAMP accumulation diminished in cells treated with cytochalasin B, CCCP and DIDS + CCCP.
  • 7.7. The adrenergic swelling of carp red cells was reduced in normoxia by DIDS. NPM and CCCP increased the adrenergic swelling in normoxia to hypoxic level.
  • 8.8. In hypoxia WGA and Anquilla lectin decreased the swelling.
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15.
  • 1.1. Using a high-speed video system operating at 400 frames/sec, the effects of temperature on tail beat frequency, swimming speed and stride length were examined in newly hatched larvae of herring (Clupea harengus L.) and in tadpole larvae of the ascidian Dendrodoa grossularia van Beneden.
  • 2.2. The effect of temperature was linear; the tail beat frequency of 8 mm-long herring larvae increased from 19 Hz at 5.6°C to 37 Hz at 14.9°C (Q10 = 2.04); that of 2 mm-long Dendrodoa larvae increased from 10 Hz at 9.6°C to 23 Hz at 18.1°C (Q10 = 2.52).
  • 3.3. Burst swimming speeds of herring larvae increased from 80 mm/sec at 5°C to 150 mm/sec at 15°C, stride length remaining constant at about 0.5 of the body length for each tail beat.
  • 4.4. More continuous swimming of Dendrodoa increased from 4.0 mm/sec at 10°C to 11.5 mm/sec at 18°C, the stride length increasing from about 0.15 to 0.25.
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16.
  • 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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17.
  • 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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18.
  • 1.1. The respiratory status of the embryonic quail during the two days prior to hatching was assessed by measuring the gas tensions within the air space of the egg and of blood collected from the chorioallantois.
  • 2.2. When the lungs became inflated there was a significant decrease in the pO2 of the gas in the air space.
  • 3.3. After pipping, there was a rise in the pO2 and fall in the pCO2 within the air space, together with corresponding changes in the blood.
  • 4.4. The outer shell membrane remained intact until the onset of hatching.
  • 5.5. These results were compared with those obtained by other workers using the domestic fowl.
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19.
  • 1.1. An alkaline p-nitrophenylphosphate phosphatase has been purified 440-fold from extracts of Hatobacterium halobium.
  • 2.2. The enzyme has an apparent molecular weight of 24,000.
  • 3.3. A Km value for p-nitrophenylphosphate of 1.12mM has been found under optimal conditions.
  • 4.4. The enzyme is selectively activated and stabilized by Mn2+.
  • 5.5. It requires high salt concentrations for stability and maximum activity.
  • 6.6. It displays an unusual restricted substrate specificity of 25 phosphate esters tested, only phosphotyrosine and casein were hydrolysed besides p-nitrophenylphosphate.
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20.
  • 1.1. The properties of ATPase activity were studied with the cells at the early stationary phase of Saccharomycopsis fibuligera.
  • 2.2. Optimal pH for the activity was approximately 7.
  • 3.3. The activity was stimulated by Mg2+.
  • 4.4. The activity was inhibited by NaF, DCCD, oligomycin, NaN3, NaVO3, or PCMB but not inhibited by ouabain.
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