Metabolic and ventilatory responses to hypoxia in two altitudinal populations of the toad, Bufo bankorensis

Effects of hypoxia on resting oxygen consumption (MO2), lung ventilation, and heart rate at different ambient PO2 were compared between lowland and high altitude populations of the toad, Bufo bankorensis. Resting MO2 decreased significantly in mild hypoxia (PO2 = 120 mm Hg) at 10 degrees C and in moderate hypoxia (PO2 = 80 mm Hg) at 25 degrees C in both altitudinal populations; however, resting MO2 did not differ significantly between the two populations. Numbers of lung ventilation periods (VP) and total inspired volume (VL) did not change with PO2 at 10 degrees C, but did increase at moderate and severe hypoxia (40 mm Hg), respectively, at 25 degrees C. Resting heart rates did not change during hypoxia and did not differ between altitude populations. The results suggest (1) the effect of PO2 change on MO2 should be considered in future studies involving transfer of anurans to a different altitude; and (2) the metabolic and ventilatory physiology in B. bankorensis does not compensate for the low temperature and PO2 at high altitude.     

Acute hypoxia alters eicosanoid production of perfused pulmonary artery endothelial cells in culture

Hypoxia alters vascular tone which regulates regional blood flow in the pulmonary circulation. Endothelial derived eicosanoids alter vascular tone and blood flow and have been implicated as modulators of hypoxic pulmonary vasoconstriction. Eicosanoid production was measured in cultured bovine pulmonary endothelial cells during constant flow and pressure perfusion at two oxygen tensions (hypoxia: 4% O₂, 5% CO₂, 91% N₂; normoxia: 21% O₂, 5% CO₂, 74% N₂). Endothelial cells were grown to confluence on microcarrier beads. Cell cartridges (N=8) containing 2 ml of microcarrier beads ( 5 × 10⁶ cells) were constantly perfused (3 ml/min) with Krebs' solutions (pH 7.4, T 37°C) equilibrated with each gas mixture. After a ten minute equilibration period, lipids were extracted (C₁₈ Sep Pak®) from twenty minute aliquots of perfusate over three hours (nine aliquots per cartridge). Eicosanoids (6-keto PGF_1α; TXB₂; and total leukotriene [LT - LTC₄, LTD₄, LTE₄, LTF₄]) were assayed by radioimmunoassay. Eicosanoid production did not vary over time. 6-keto PGF_1α production was increased during hypoxia (normoxia 291 ± 27 vs hypoxia 395 ± 35 ng/min/gm protein; p < 0.01). Thromboxane production (normoxia 19 ± 2 vs hypoxia 20 ± 2 ng/min/gm protein) and total leukotriene production (normoxia 363 ± 35 vs hypoxia 329 ± 29 ng/min/gm protein) did not change with hypoxia. These data demonstrated that oxygen increased endothelial prostacyclin production but did not effect thromboxane or leukotriene production.     

The influence of chronic anaemia on catecholamine secretion in the rainbow trout (Oncorhynchus mykiss)

The effect of long-term (7 day) anaemia on catecholamine release was examined in rainbow trout (Oncorhynchus mykiss) in vivo during acute exposure to hypoxia and in situ using a perfused post-cardinal vein preparation. The first goal was to distinguish among reductions in blood O₂ partial pressure, O₂ concentration and haemoglobin percentage saturation as potential stimuli for, or correlates of, catecholamine secretion during hypoxia. The second goal was to elucidate the role of these factors in promoting enhanced chromaffin cell responsiveness in trout subjected to chronic hypoxia (Montpetit and Perry 1998). Anaemic fish (haematocrit lowered from 28.4±2.4% to 11.9±1.6%) displayed a marked reduction in haemoglobin-O₂ binding affinity [P ₅₀ (P _aO₂ at 50% Hb-O₂ saturation) was increased from 14.7 mm Hg to 24.3 mm Hg]. Upon exposure to hypoxia, the anaemic fish released catecholamines into their circulation at higher values of arterial O₂ partial pressure (∼52 mm Hg versus ∼18 mm Hg) and haemoglobin O₂ saturation (<70% versus <55%) than did control fish. In addition, anaemic fish achieved significantly greater circulating levels of total catecholamines (noradrenaline plus adrenaline) during acute hypoxia (294.8±67.3 versus 107.0±35.6 nmol l⁻¹). These results do not support the view that catecholamine release is triggered by a reduction in haemoglobin O₂ saturation or arterial PO₂, per se. Nor are they consistent with the idea that catecholamine release occurs at a threshold value of arterial PO₂ corresponding to a critical reduction in blood O₂ concentration. The effects of the non-selective cholinergic receptor carbachol on catecholamine secretion from chromaffin tissue were assessed using perfused posterior cardinal vein preparations derived from control or anaemic fish. For adrenaline secretion, there was no statistically significant change in the ED₅₀ (dose eliciting 50% response). For noradrenaline secretion however, preparations originating from anaemic fish displayed an enhanced responsiveness to carbachol as indicated by a significant 4.5-fold reduction in the carbachol ED₅₀ value from 2.53 × 10⁻⁶ mol kg⁻¹ to 5.67 × 10⁻⁷ mol kg⁻¹. These results demonstrate that anaemia-induced hypoxaemia, in the absence of any lowering of PO₂, is able to modulate the responsiveness of chromaffin cells to cholinergic stimulation. Accepted: 21 April 1999     

Aerobic capacity of Peruvian Quechua: A test of the developmental adaptation hypothesis

High altitude natives are reported to have outstanding work capacity in spite of the challenge of oxygen transport and delivery in hypoxia. To evaluate the developmental effect of lifelong exposure to hypoxia on aerobic capacity, VO_2peak was measured on two groups of Peruvian Quechua subjects (18–35 years), who differed in their developmental exposure to altitude. Male and female volunteers were recruited in Lima, Peru (150 m), and were divided in two groups, based on their developmental exposure to hypoxia, those: a) Born at sea‐level individuals (BSL), with no developmental exposure to hypoxia (n = 34) and b) Born at high‐altitude individuals (BHA) with full developmental exposure to hypoxia (n = 32), but who migrated to sea‐level as adults (>16‐years‐old). Tests were conducted both in normoxia (BP = 750 mm Hg) and normobaric hypoxia at sea‐level (BP = 750 mm Hg, FiO₂ = 0.12, equivalent to 4,449 m), after a 2‐month training period (in order to control for initial differences in physical fitness) at sea‐level. BHA had a significantly higher VO_2peak at hypoxia (40.31 ± 1.0 ml/min/kg) as compared to BSL (35.78 ± 0.96 ml/min/kg, P = 0.001), adjusting for sex. The decrease of VO_2peak at HA relative to SL (ΔVO_2peak) was not different between groups, controlling for baseline levels (VO_2peak at sea‐level) and sex (BHA = 0.35 ± 0.04 l/min, BSL = 0.44 ± 0.04 l/min; P = 0.12). Forced vital capacity (controlling for height) and the residuals of VO_2peak (controlling for weight) had a significant association in the BHA group only (r = 0.155; P = 0.031). In sum, results indicate that developmental exposure to altitude constitutes an important factor to determine superior exercise performance. Am J Phys Anthropol 156:363–373, 2015. © 2014 Wiley Periodicals, Inc.     

Blood respiratory properties of rainbow trout,Salmo gairdneri: Responses to hypoxia acclimation and anoxic incubation of blood in vitro

Summary Blood respiratory properties of rainbow trout were determined following acclimation to normoxia and two levels of hypoxia.The most prominent response appeared to be an increase in blood O₂ affinity graded to the level of hypoxia. TheP ₅₀ values (at pH 7.8 and 20°C) were 24.1 21.7 and 16.8 mm Hg when specimens were acclimated to water O₂ tensions of 150, 80 and 50 mm Hg, respectively. The blood O₂ affinity was closely correlated with the erythrocytic ATP concentration. The stepwise correlation of ATP andP ₅₀, when trout were exposed to graded oxygen lack in the water, indicates that the blood O₂ affinity is precisely regulated.Anoxic incubation of trout blood in vitro induced a rapid reduction in erythrocytic ATP concentration (t _1/2=75 min), which was closely correlated to theP ₅₀ value. The drop inP ₅₀ value during anoxic exposure can be explained partly by the direct allosteric effect of a decreased erythrocytic ATP concentration and partly by the modified Donnan distribution of protons across the red cell membrane. Reoxygenation of the incubated blood, however, only partly re-established the erythrocytic ATP concentration, with a concurrent rise inP ₅₀ value.The results invite discussion about the mechanism, by which fish regulate their blood O₂ affinity. It is concluded, that it is regulated at the organismal rather than at the red cell level.Abbreviation (E) erythrocytes, erythrocytic     

The influence of hypoxia on the blood regulation of the brackish water shrimp Palaemonetes varians Leach

During periods of hypoxia in hypotonic media, Palaemonetes varians Leach showed an unimpaired regulation of blood chloride until some minutes before death. Heart rate showed no clear dependence on the water oxygen tension (P_wO₂) and postbranchial haemolymph oxygen tensions slowly decreased during progressive hypopoxia from a normoxic level of ≈ 30 mm Hg until the animals turned opaque some minutes before they died. Blood pH increased in hypoxia, from 7.6 in normoxia to > 8 in P_wO₂ 10 mm Hg. Taken together, these data have been taken to indicate that the oxygen consumption rate at the critical point (MO₂ P_cr) of this species is very low (P_wO₂ = < 10 mm Hg) compared with other brackish water natantians studied. The ecological significance of this to the species is considered.     

Metabolic responses during initial days of altitude acclimatization in the Eastern Himalayas

The study was carried out on 16 men (aged 20–30 years) to evaluate daily metabolic responses during the early phase of altitude acclimatization at moderate altitudes between 3100 and 4200 m in the Eastern Himalayas. Resting (R) and submaximal exercise (E) oxygen consumption (|VO₂) at 100 W at sea level (SL) were 3.25 (SEM 0.15) and 20.31 (SEM 0.77) ml/kg per min respectively. On day 1 at 3110 m both R and E |VO₂ decreased (P<0.001) and subsequently remained constant. At 3445 m these values tended to increase over the 3110 m values but were lower than the SL values. At 4177 m the decline in |VO₂ was significantly greater (P<0.01) than at the preceding altitudes. Pulmonary ventilation (|VE) increased consistently (P<0.001) with increase in altitude. The arterial oxygen saturation (S _a O₂) at different altitudes was lower (P<0.001) than SL values. The cardiac frequency (f _C ) at R and E was higher (P<0.001) at altitude; the values at 3110 and 3445 m were significantly lower (P<0.001) than at 4177 m. Blood pressure (BP) increased (P<0.001) on the first day at each altitude. The systolic BP tended to decline towards SL values but the diastolic BP remained high (P<0.001) throughout. The resting blood lactic acid concentration, [la ^–] _bl , showed a decline (P<0.001) only at 4177 m. The [la ^–] _bl at E was similar at 3110 and 3445 m but was higher (P<0.01) at 4177 m. These observations suggest that acclimatization to a mid-altitude of 3445 m can be safely avoided where rapid ascent to higher altitude is required.     

Effects of ambient PO2 and temperature on oxygen uptake in Nautilus pompilius

This study employs closed-circuit respirometry to evaluate the effect of declining ambient oxygen partial pressure (PO₂) and temperature on mass specific rates of oxygen uptake (V˙O₂) in Nautilus pompilius. At all temperatures investigated (11, 16, and 21 °C), V˙O₂ is relatively constant at high PO₂ (oxyregulation) but declines sharply at low PO₂ (oxyconformation). The critical PO₂ below which oxyconformation begins (P _c) is temperature dependent, higher at 21 °C (49 mmHg) than at 11 °C or 16 °C (21.7 mmHg and 30.8 mmHg respectively). In resting, post-absorptive animals, steady-state resting V˙O₂ increases significantly with temperature resulting in a Q₁₀ value of approximately 2.5. The metabolic strategy of N. pompilius appears well suited to its lifestyle, providing sufficient metabolic scope for its extensive daily vertical migrations, but allowing for metabolic suppression when PO₂ falls too low. The combination of low temperatures and low PO₂ may suppress metabolic rate 16-fold (assuming negligible contributions from anaerobic metabolism and internal O₂ stores), enhancing hypoxia tolerance. Accepted: 20 January 2000     

In vitro studies of the effect of Environmental Conditions on the anthacnose pathogen of bananas, Colletotrichum musae

In vitro studies were undertaken to determine the effect of pH, temperature, water availability and carbon dioxide (CO₂) concentration on germination and growth of Colletotrichum musae, the causal pathogen of anthracnose of bananas. The optimum pH for germination and growth varied between 4·0 and 5·0 depending on temperature. At low pH (< 3·0) and 15°C, both germination and growth were significantly reduced, with a marked increase in the lag time, in days, prior to growth. C. musae germinated and grew over a wide range of water activities (a_w; 0·995−0·94 and 0·995−0·92, respectively) at 20, 25 and 30°C. In all cases where germination occurred appresoria were subsequently produced. Optimum growth occurred at 30°C and 0·995 a_w, although this changed to 0·98 a_w at 35°C. Increasing CO₂ concentration to 15% or reducing oxygen concentration to 1% resulted in a significant (P < 0·05) reduction in growth, but did not inhibit growth completely.     

Oxygen uptake of carp,Cyprinus carpio,swimming in normoxic and hypoxic water

Synopsis Oxygen uptake (V_{o 2}) was measured in carp of approximately 40 cm length swimming at controlled variable oxygen tensions (P_{o 2}). At P_{o 2}> 120 mm Hg V_{o 2} increased with an increase in swimming speed from 5.6 to 11.3 cm · sec^–1. Extrapolation of V_{o 2} to zero activity at P_{o 2} = 140 mm Hg revealed a standard O₂ uptake of 36.7 ml O₂ · kg^–1 · h^–1 at 20° C. At the lowest swimming speed (5.6 cm · s^–1) the oxygen uptake increased when the water P_{o 2} was reduced. A near doubling in V_{o 2} was seen at P_{o 2} = 70 mm Hg compared to 140 mm Hg. At higher swimming speeds in hypoxic water V_{o 2} decreased relative to the values at low swimming speeds. As a result the slope of the lines expressing log V_{o 2} as a function of swimming speed decreased from positive to negative values with decreasing P_{o 2} of the water. pH of blood from the caudal vein drawn before and at termination of swimming at P_{o 2} = 70 mm Hg and 100 mm Hg did not show any decrease in relation to rest values at P_{o 2} = 140 mm Hg. Blood lactate concentration did not increase during swimming at these tensions.     

An investigation of the role of circulating catecholamines in the control of ventilation during acute moderate hypoxia in rainbow trout (Oncorhynchus mykiss)

Summary Gill ventilation volume ( w), arterial blood oxygen tension (PaO₂) and arterial blood oxygen content (CaO₂) of rainbow trout (Oncorhyncus mykiss) were monitored during normoxia [waterPO₂ (PwO₂) 155 Torr], hypoxia (PwO₂=72±5.8 Torr), or hyperoxia (PwO₂=643±32 Torr). Fish hyperventilated during acute (30 min) hypoxia and hypoventilagted during acute hyperoxia. Plasma catecholamine levels were unchanged after 30 min of hypoxia or hyperoxia. In addition, selective adrenoceptor blockade with either propranolol (-adrenoceptor antagonist) or phentolamine (-adrenoceptor antagonist) did not modify the hyperventilatory response during hypoxia. These results indicate that circulating catecholamines are not involved in the control of ventilation in moderately hypoxic rainbow trout. In the summer, intra-arterial infusion of catecholamine in normoxic trout caused transient (adrenaline) or persistent (noradrenaline) hypoventilation. These observations also do not support a role for catecholamines in the stimulation of ventilation.During hypoxia,PwO₂,PaO₂ andCaO₂ were depressed whereas during hyperoxia, onlyPwO₂ andPaO₂ was elevated significantly. Thus, it is suggested that the hypoventilatory response to hyperoxia is mediated by a direct effect of elevatedPwO₂/PaO₂, whereas the hyperventilatory response to hypoxia is mediated by changes inPwO₂/PaO₂, and/orCaO₂.     

The influence of dissolved oxygen concentration on phosphofructokinase and the glucose metabolism ofEscherichia coli K-12

The glucose metabolism and the response of phosphofructokinase activity to oxygen were investigated using glucose-limited chemostat cultures ofE. coli K-12. With a dilution rate of 0.2 hr^–1 and a glucose input concentration of 0.83 g/litre, 10 steady states were obtained ranging from 320 to 0 mm HgO₂. Dissolved oxygen reached zero level at a pO₂ of 25.8 mm Hg. The specific phosphofructokinase activity was constant above 28 mm Hg O₂ and increased linearly at lower pO₂ levels until it reached highest activity at 0 mm Hg O₂. Cell dry weight also started to decrease linearly from 28 to 5.9 mm Hg O₂, and fell sharply thereafter. Acid production rate did not start before pO₂ reached 25.6 mm Hg, increased progressively with an additional sharp increase below 5.9 mm Hg O₂. The main endproducts formed were acetic acid and ethanol with lactic acid appearing below 5.9 mm Hg O₂. The results suggest an effect of oxygen on phosphofructokinase synthesis rather than an ATP inhibition of the enzyme.This work was supported by a grant from the Australian Research Grant Commission.     

Respiratory and cardiovascular responses to acute hypoxia and hyperoxia in internally pipped chicken embryos

During the first day of hatching, the developing chicken embryo internally pips the air cell and relies on both the lungs and chorioallantoic membrane (CAM) for gas exchange. Our objective in this study was to examine respiratory and cardiovascular responses to acute changes in oxygen at the air cell or the rest of the egg during internal pipping. We measured lung (V·_O2lung) and CAM (V·_O2CAM) oxygen consumption independently before and after 60 min exposure to combinations of hypoxia, hyperoxia, and normoxia to the air cell and the remaining egg. Significant changes in V·_O2total were only observed with combined egg and air cell hypoxia (decreased V·_O2total) or egg hyperoxia and air cell hypoxia (increased V·_O2total). In response to the different O₂ treatments, a change in V·_O2lung was compensated by an inverse change in V·_O2CAM of similar magnitude. To test for the underlying mechanism, we focused on ventilation and cardiovascular responses during hypoxic and hyperoxic air cell exposure. Ventilation frequency and minute ventilation (V_E) were unaffected by changes in air cell O₂, but tidal volume (V_T) increased during hypoxia. Both V_T and V_E decreased significantly in response to decreased P_CO2. The right-to-left shunt of blood away from the lungs increased significantly during hypoxic air cell exposure and decreased significantly during hyperoxic exposure. These results demonstrate the internally pipped embryo's ability to control the site of gas exchange by means of altering blood flow between the lungs and CAM.     

Temperaturadaptation der Sauerstoffaffinität des Blutes von Rana esculenta L.

Zusammenfassung Die Sauerstoffaffinität des Blutes (ausgedrückt im Sauerstoffhalbsättigungsdruck P ₅₀) von an 5° C adaptierten Fröschen (Rana esculenta L.) ist bei gleicher Umgebungstemperatur geringer als bei an 20° C adaptierten Fröschen. P ₅₀ bei pH 7,4 und 20° C Umgebungstemperatur betrug 42,4 mm Hg bei den kälte- und 39,1 mm Hg bei den wäremadaptierten Fröschen (Abb. 1). Die Sauerstoffkapazität der kälteangepaßten Frösche von 12,33 ml O₂/100 ml Blut ist höher als die der wärmeangepaßten von 10,43 ml O₂/100 ml Blut (Tabelle 1). Die Bedeutung und die Ursache der Sauerstoffkapazitäts- und Sauerstoffaffinitätsadaptation im Hinblick auf die Stoffwechseladaptation werden diskutiert.

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Temperature adaptation of the oxygen affinity of the blood in Rana esculenta L.

Summary The oxygen affinity of blood (expressed by the oxygen half saturation pressure P ₅₀) in frogs (Rana esculenta L.), adapted to 5° C is less as in frogs, adapted to 20° C at equal experimental temperature. P ₅₀ in cold-adapted frogs related to pH 7.4 and 20° C is 42.4 mm Hg and in heat-adapted frogs 39.1 mm Hg (Fig. 1). The oxygen capacity of the cold-adapted frogs is with 12.33 ml O₂/100 ml blood higher than of the heat-adapted frogs with 10.43 ml O₂/100 ml blood (Table 1). The importance and the origin of the adaptation of the oxygen affinity and capacity in view to the adaptation of the metabolic rate are discussed.

     

Respiration and oxygen transport functions of the blood from an intertidal fish,Helcogramma medium (Tripterygiidae)

Synopsis Aquatic and aerial oxygen uptake (̇O₂), ventilation frequency, and oxygen transport properties of the blood were determined for the intertidal fish Helcogramma medium. Ventilation frequency increased in response to decreased environmental PO₂ and aquatic ̇O₂ was maintained down to a critical PO₂ of 30–40 mm Hg. Below PO₂ 30 mm Hg fish intermittently gulped air and finally emerged into air at PO₂ 18 mm Hg. After 1 h exposure to air ̇O₂ decreased to 60% of the aquatic rate and this was accompanied by an increase in blood lactate. Aerobic expansibility was reduced in air (×1.2) compared to water (× 5.5). The Hb concentration was 0.47 ± 0.13 mmol 1^–1 and hematocrit 11.55 ± 3.61% indicating a moderate O₂-carrying capacity. Oxygen affinity was not especially high (P₅₀ = 19 mm Hg at pH 7.7 and 15°C) and ATP was the predominant acid-soluble phosphate regulating P₅₀. The equilibrium curve was essentially hyperbolic (Hill's n = 1.2) with a marked Bohr effect = –1.06) and Root effect (saturation depressed by 50% at pH7.1). The pattern of respiration and the respiratory properties of the blood together with observations of the behaviour of the fish during aerial exposure indicated that Helcogramma is adapted to living in a well-aerated environment yet can adequately tolerate short term exposure to low aquatic PO₂ or air.     

Effect of hypoxia on prostacyclin production in cultured pulmonary artery endothelium

Exposure of cultured bovine pulmonary artery endothelial cells to varying levels of hypoxia (10% or 0% O₂) for 4 hours resulted in a significant dose-dependent inhibition in endothelial prostacyclin synthesis (51% and 98%, at the 10% and 0% O₂ levels respectively, p <0.05, compared to 21% O₂ exposure values). Release of ³H-arachidonic acid from cellular pools was not altered by hypoxia. Some of the cells were incubated with arachidonic acid (20 μM for 5 min) or PGH₂ (4 μM for 2 min) immediately after exposure. Endothelium exposed to 0% O₂, but not to 10% O₂, produced significantly less prostacyclin after addition of either arachidonic acid (25 ± 5% of 21% O₂ exposure values, n=6, p <0.01) or PGH₂ (31 ± 3% of 21% O₂ exposure values, n=6, p <0.05). These results suggest that hypoxia inhibits cyclooxygenase at the 10% O₂ level and both cyclooxygenase and prostacyclin synthetase enzymes at the 0% O₂ exposure levels. Exposure of aortic endothelial cells resulted in a 44% inhibition of prostacyclin at the 0% exposure level. No significant alteration in prostacyclin production was found in pulmonary vascular smooth muscle cells exposed to hypoxia. These data suggest that the increased prostacyclin production reported in lungs exposed to hypoxia is not due to a direct effect of hypoxia on the main prostacyclin producing cells of the pulmonary circulation.     

Seasonal respiratory responses to temperature and hypoxia in relation to burrowing depth in three intertidal bivalves

Respiratory responses to temperature and hypoxia in relation to burrowing depth were determined for winter- (W-C) and summer-conditioned (S-C) individuals of , , and . These bivalves occur sympatrically on sand-flats but display different sediment burrowing depths ( . , <2 cm; . , 3–8 cm; . , 5–20 cm). A range depths over which daily temperature variation and O₂ concentration decline rapidly from surface values. Species thermal tolerance limits were found to decrease and to be more greatly temperature compensated with burrowing depth. Oxygen consumption rate (VO₂ increased with temperature to 25°C in . , but was, thereafter, regulated (Q10 1.0) up to 40°C while VO₂ increased with temperature in . and . until thermally streased at 25° to 30°C. The deposit feeding . does not acclimate VO₂ to temperature while . and . , both suspension feeders, show “reverse” acclimation [VO₂ (W-C) < VO₂ (S-C)] that conserves overwintering energy stores. The shallow burrowing . and deposit feeding . rarely experience hypoxia and are poor to non-regulators of VO₂ in reduced O₂ concentrations. In contrast, when winter-conditioned, . is a moderate regulator of VO₂, the degree of regulation increasing in S-C individuals which are exposed to higher levels of hypoxia.     

Respiratory responses and tolerance to hypoxia in two marine teleosts,Epinephelus akaara (Temminck & Schlegel) and Mylio macrocephalus (Basilewsky)

The respiratory responses and tolerance of hypoxia were studied in two marine teleosts, the red grouper (Epinephelus akaara, a sluggish species) and the black sea bream (Mylio macrocephalus, an active species). Neither species showed abnormal behaviour or mortality when exposed to 2 mg O₂ l^–1 for 7 h. The black sea bream was, however, comparatively more tolerant when exposed to 1 mg O₂ l^–1, but tolerance of both species became similar under extremely hypoxic conditions (i.e. 0.5 mg O₂ l^–1). In contrast to most other teleosts, both species showed a reduction in opercular beating rate during hypoxia, and oxygen conformity was found in the range of 0.5 to 7.0 mg O₂l ^–1. O₂ dissociation curves were constructed, and the P₅₀ value of the black sea breams (27 ± 5.6 mm Hg) was found to be much lower than that of the red groupers (50 ± 2.5 mm Hg). For both species, the general levels of venous PO₂ showed a direct relationship to ambient PO₂, and were markedly reduced after 1 h exposure to various levels of hypoxia. Compared with the red groupers, the black sea breams appeared to be more able to maintain its venous PO₂ levels during prolonged hypoxic exposure.     

Thyroid function during intermittent exposure to hypobaric hypoxia

Circulatory levels of triiodothyronine (T₃) and thyroxine (T₄) and their kinetics were studied in rabbits exposed to intermittent hypobaric hypoxia (5200 m, 395 mm Hg,PO₂ 83 mm Hg) 6 h daily for 5 weeks in a decompression chamber maintained at room temperature of 22°–24° C. Kinetics of T₃ and T₄ were studied on days 21 and 28 of hypoxic exposure. The T₃ and T₄ values were found to be significantly lower on day 8 of exposure to hypoxia compared to the pre-exposure values. The decreased levels were maintained throughout the entire period of hypoxic stress. The metabolic clearance rate, production rate, distribution space and extrathyroidal T₃ and T₄ pools were significantly decreased in animals under hypoxic stress compared to the control animals. The decline in thyroid hormone levels and their production in rabbits under hypoxic stress indicate an adaptive phenomenon under conditions of low oxygen availability.     

Transposition of Saccharomyces cerevisiae Ty1 retrotransposon is activated by improper cryopreservation

Ty1 is a retrotransposon of the yeast Saccharomyces cerevisiae whose transposition at new locations in the host genome is activated by stress conditions, such as exposure to UV light, X-rays, nitrogen starvation. In this communication, we supply evidence that cooling for 2 h at +4 °C followed by freezing for 1 h at −10 °C and 16 h at −20 °C also increased Ty1 transposition. The mobility of Ty1 was induced by cooling at slow rates (3 °C/min) and the accumulation of trehalose inside cells or the cooling at high rates (100 °C/min) inhibited significantly the induction of the transposition. The freeze-induced Ty1 transposition did not occur in mitochondrial mutants (rho⁻) and in cells with disrupted SCO1 gene (Δsco1 cells) evidencing that the Ty1 transposition induced by cooling depends on the mitochondrial oxidative phosphorylation. We also found that the freeze induced Ty1 transposition is associated with increased synthesis and accumulation of superoxide anions (O⁻₂) into the cells. Accumulation of O⁻₂ and activation of Ty1 transposition were not observed after cooling of cells with compromised mitochondrial functions (rho⁻, Δsco1), or in cells pretreated with O⁻₂ scavengers. It is concluded that (i) elevated levels of reactive oxygen species (ROS) have a key role in activation the transposition of Ty1 retrotransposon in yeast cells undergoing freezing and (ii) given the deleterious effect of increased ROS levels on cells, special precautions should be taken to avoid ROS production and accumulation during cryopreservation procedures.