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Temperature acclimation modifies Na+ current in fish cardiac myocytes.

The present study was designed to test the hypothesis that temperature acclimation modifies sarcolemmal Na+ current (INa) of the fish cardiac myocytes differently depending on the animal's lifestyle in the cold. Two eurythermal fish species with different physiological strategies for surviving in the cold, a cold-dormant crucian carp (Carassius carassius L.) and a cold-active rainbow trout (Oncorhynchus mykiss), were used in acclimation experiments. The INa of carp and trout were also compared with INa of a cold stenothermal burbot (Lota lota). In accordance with the hypothesis, cold-acclimation decreased the density of INa in crucian carp and increased it in rainbow trout, suggesting depression of impulse conduction in cold-acclimated carp and positive compensation of impulse propagation in cold-acclimated trout. The steady-state activation curve of trout INa was shifted by 6 mV to more negative voltages by cold acclimation, which probably lowers the stimulus threshold for action potentials and further improves cardiac excitability in the cold. In burbot myocytes, the INa density was high and the position of the steady-state activation curve on the voltage axis was even more negative than in trout or carp myocytes, suggesting that the burbot INa is adapted to maintain high excitability and conductivity in the cold. The INa of the burbot heart differed from those of carp and trout in causing four times larger charge influx per excitation, which suggests that INa may also have a significant role in cardiac excitation-contraction coupling of the burbot heart. In summary, INa of fish cardiac myocytes shows thermal plasticity that is different in several respects in cold-dormant and cold-active species and thus has a physiologically meaningful role in supporting the variable life styles and habitat conditions of each species.

Acclimatization↗

The relative contributions of developmental plasticity and adult acclimation to physiological variation in the tsetse fly, Glossina pallidipes (Diptera, Glossinidae).

Recent reviews of the adaptive hypotheses for animal responses to acclimation have highlighted the importance of distinguishing between developmental and adult (non-developmental) phenotypic plasticity. There has been little work, however, on separating the effects of developmental plasticity from adult acclimation on physiological traits. Therefore, we investigated the relative contributions of these two distinct forms of plasticity to the environmental physiology of adult tsetse flies by exposing developing pupae or adult flies to different temperatures and comparing their responses. We also exposed flies to different temperatures during development and re-exposed them as adults to the same temperatures, to investigate possible cumulative effects. Critical thermal maxima were relatively inflexible in response to acclimation temperatures (21, 25, 29 degrees C) with plasticity type accounting for the majority of the variation (49-67%, nested ANOVA). By contrast, acclimation had a larger effect on critical thermal minima with treatment temperature accounting for most of the variance (84-92%). Surprisingly little of the variance in desiccation rate could be explained by plasticity type (30-47%). The only significant effect of acclimation temperature on standard (resting) metabolic rate of adult flies was at 21 degrees C, resulting in treatment temperature, rather than plasticity type, accounting for the majority of the variance (30-76%). This study demonstrates that the stage at which acclimation takes place has significant, though often different, effects on several adult physiological traits in G. pallidipes, and therefore that it is not only important to consider the form of plasticity but also the direction of the response and its significance from a life-history perspective.

Acclimatization↗

Acclimation of the euryhaline toad Bufo viridis to hyperosmotic solution (NaCl, urea and mannitol).

Bufo viridis were acclimated to hyperosmotic solutions of NaCl, urea or mannitol. The toads could not be acclimated to mannitol solutions of osmotic strength higher than 300 mosmol kg-1 H2O, but could be acclimated easily to NaCl and urea higher than 500 mosmol kg-1 H2O. Water uptake diminished under mannitol acclimation while the apparent osmotic permeability under NaCl and urea acclimation increased. Urea and sodium influx across the isolated skin changed inversely upon hyperosmotic acclimation, but they did not seem to depend on one another. The adaptational advantages of the observed changes are discussed.

Adaptation, Physiological↗

The temperature dependence of the time course of growth and decay of miniature end-plate currents in carp extraocular muscle following thermal acclimation.

1. The effect of temperature (5-35 degrees C) on the decay and growth phases of miniature end-plate currents (MEPCs) was investigated in extraocular muscle from freshwater carp acclimated to either high (28 degrees C) or low (8 degrees C) temperature. 2. The temperature dependence of the time constant of decay (TD) was found to follow an Arrhenius relationship; the relationship between logTD and reciprocal of absolute temperature (1/K) being linear in both groups. The TD of MEPCs recorded from cold-acclimated carp was not statistically significant from that of the warm group. 3. TD was moderately temperature-dependent. Regression gave a Q10 of 1.78 for the warm-acclimated carp, corresponding to an activation energy, Ea, of 41.15 +/- 2.17 kJ mol-1. For the cold-acclimated carp, the Q10 was 1.79, and Ea was 41.43 +/- 2.46 kJ mol-1. 4. Growth time (TG) was less susceptible than TD to temperature change. The relationship between growth time (taken as the time for MEPCs to rise from 20 to 80% of maximum) and temperature was linear for the cold-acclimated group, with a Q10 of 1.34 and Ea of 20.94 +/- 4.75 kJ mol-1. The data for the warm group, were, in contrast, best fitted by two linear regressions meeting at 15.1 degrees C. At temperatures below 15.1 degrees C Q10 was 3.16 and Ea was 82.20 +/- 15.47 kJ mol-1; above 15 degrees C, Q10 was 1.22 and Ea was 14.15 +/- 12.24 kJ mol-1. 5. The acetylcholinesterase inhibitor neostigmine increased TD by approximately twofold and raised TG to approximately 1.4 times control values. These effects were observed across the temperature range scanned for both groups. 6. The results are discussed with reference to the documented effects of temperature and temperature acclimation on membrane lipids and proteins.

Acclimatization↗

THERMAL ACCLIMATION, NEUROMUSCULAR SYNAPTIC DELAY AND MINIATURE END-PLATE CURRENT DECAY IN THE FROG RANA TEMPORARIA

1. The effects of 1 or 2­3 weeks of acclimation to 4 °C and 24 °C of overwintering grass frogs (Rana temporaria) on the synaptic delay and on the time constant of the decay phase (tau) of miniature end-plate currents (MEPCs) in the neuromuscular junction of sartorius muscle were studied. In order to equalize the possible effects of differential starvation, the animals were usually cross-acclimated to the two temperatures. 2. Synaptic delay was not affected by temperature acclimation but was slightly prolonged by the more profound starvation at the higher temperature when the cross-acclimation procedure was not used. The average Q10 of synaptic delay between 4 and 24 °C was 2.60 and of minimum synaptic delays, 2.64. The corresponding values for apparent activation energy (Ea) were 65.79 and 66.48 kJ mol-1. 3. The time constant of the decay phase of MEPCs was not affected by temperature acclimation. The average Q10 between 4 and 24 °C was 2.27. The corresponding Ea value was 56.02 kJ mol-1. 4. The function of peripheral neuromuscular synapses is well regulated and changes in its time relationships do not appear to be involved in the thermal acclimation of frogs.

Journal Article↗

The cardiovascular responses of the red-eared slider (Trachemys scripta) acclimated to either 22 or 5 degrees C. I. Effects of anoxic exposure on in vivo cardiac performance.

The extreme anoxia-tolerance of freshwater turtles under cold conditions is well documented, but little is known about their cardiac performance in such situations. Using chronic catheterization techniques, we measured systemic cardiac power output (PO(sys)), systemic cardiac output (Q(.)(sys)), heart rate (fh), systemic stroke volume (V(s,sys)), systemic resistance (R(sys)) and mean arterial pressure (P(sys)) in red-eared sliders (Trachemys scripta). The effects of cold acclimation and anoxic exposure were studied. Turtles were acclimated to either 22 degrees C or 5 degrees C, and the anoxic exposure was either acute (6 h) at 22 degrees C or chronic (3 weeks) at 5 degrees C. Cold acclimation alone decreased PO(sys) by 15-fold, representing a Q(10) of 8.8. In addition, fh and V(s,sys) decreased significantly, while R(sys) increased and moderated the arterial hypotension. Acute and chronic anoxic exposures significantly decreased PO(sys), V(s,sys), fh and P(sys) and increased R(sys). But the changes were qualitatively much larger with chronic anoxia. For example, acute anoxia in 22 degrees C-acclimated turtles decreased PO(sys) by 6.6-fold, whereas chronic anoxia in 5 degrees C-acclimated turtles decreased PO(sys) by 20-fold. The remarkable cardiovascular down-regulation that accompanies long periods of cold anoxia in these turtles was characterized by comparing cardiovascular status during chronic anoxia at 5 degrees C with that during normoxia at 22 degrees C. Cardiac PO(sys) was reduced 330-fold, through decreases in Q(.)(sys) (120-fold), fh (24.2-fold), V(s,sys) (5.7-fold) and P(sys) (2. 2-fold), while R(sys) was increased 64.6-fold. We also compared cardiac glycolytic rates by assuming that PO(sys) was proportional to ATP supply and that glycolysis yielded 18 times less ATP per mole of glucose than oxidative metabolism. At 22 degrees C, the 6.6-fold decrease in PO(sys) with anoxia suggests that a Pasteur effect was needed in cardiac tissues during acute anoxia. However, this would not be so with chronic anoxia at 5 degrees C because of the 22-fold decrease in PO(sys). We propose that the suppression of the Pasteur effect and the large Q(10) values for cold acclimation would conserve glucose stores and enable turtles to withstand anoxia much longer under cold than under warm conditions.

Adaptation, Physiological↗

Possible biphasic sweating response during short-term heat acclimation protocol for tropical natives.

The aim of the present study was to evaluate the sweat loss response during short-term heat acclimation in tropical natives. Six healthy young male subjects, inhabitants of a tropical region, were heat acclimated by means of nine days of one-hour heat-exercise treatments (40+/-0 degrees C and 32+/-1% relative humidity; 50% (.)VO(2peak) on a cycle ergometer). On days 1 to 9 of heat acclimation whole-body sweat loss was calculated by body weight variation corrected for body surface area. On days 1 and 9 rectal temperature (T(re)) and heart rate (HR) were measured continuously, and rating of perceived exertion (RPE) every 4 minutes. Heat acclimation was confirmed by reduced HR (day 1 rest: 77+/-5 b.min(-1); day 9 rest: 68+/-3 b.min(-1); day 1 final exercise: 161+/-15 b.min(-1); day 9 final exercise: 145+/-11 b.min(-1), p<0.05), RPE (13 vs. 11, p<0.05) and T(re) (day 1 rest: 37.2+/-0.2 degrees C; day 9 rest: 37.0+/-0.2 degrees C; day 1 final exercise: 38.2+/-0.2 degrees C; day 9 final exercise: 37.9+/-0.1 degrees C, p<0.05). The main finding was that whole-body sweat loss increased in days 5 and 7 (9.49+/-1.84 and 9.56+/-1.86 g.m(-2).min(-1), respectively) compared to day 1 (8.31+/-1.31 g.m(-2).min(-1), p<0.05) and was not different in day 9 (8.48+/-1.02 g.m(-2).min(-1)) compared to day 1 (p>0.05) of the protocol. These findings are consistent with the heat acclimation induced adaptations and suggest a biphasic sweat response (an increase in the sweat rate in the middle of the protocol followed by return to initial values by the end of it) during short-term heat acclimation in tropical natives.

Acclimatization↗

Effects of norepinephrine on uptake and oxidation of plasma free fatty acids in cold-acclimated rats.

In order to know the mode of action of norepinephrine in enhanced utilization of plasma free fatty acids (FFA) in cold acclimation, albumin-bound 14C-palmitate was infused intravenously at a constant rate into cold- and warm-acclimated rats under pentobarbital anesthesia with and without norepinephrine infusion. Rectal temperature, CO2 output and plasma FFA, from which the rates of FFA uptake and oxidation were calculated, were determined simultaneously. Similar fractions, that is, 7 and 5% of the total uptake of plasma FFA by the tissue were immediately oxidized in both cold- and warm-acclimated rats, respectively. Norepinephrine infusion caused a significant increase in all the parameters examined. In addition, during hormone infusion the percentage of FFA uptake oxidized was elevated from 22% in control to 50% in cold-acclimated rats. This increment was accompanied with greater increases in rectal temperature and CO2 output. Similarly, in functionally eviscerated cold-acclimated rats, norepinephrine induced a greater increase in the percentage of FFA uptake oxidized than in eviscerated controls. These results indicate that although the FFA uptake was increased simultaneously norepinephrine infusion casued a more marked acceleration of the oxidation of plasma FFA in the cold-acclimated rats than in control rats.

Acclimatization↗

Comparative disposition and biotransformation of naphthalene in fresh- and seawater-acclimated striped bass (Morone saxatilis).

1. The disposition and biotransformation of naphthalene in striped bass (Morone saxatilis) acclimated to either fresh- or seawater have been determined. 2. The 24-h total concentration factor did not significantly differ between the freshwater (283.7 +/- 61.5 [+/- SD]) and seawater (245.5 +/- 44.4)-acclimated bass. At both salinities, the viscera/gonad and liver accumulated large concentrations of residues, whereas the skin retained the largest total residue mass. 3. During the 24-h depuration period, the freshwater-acclimated bass depurated 45% of retained residue and the seawater-acclimated bass depurated 85% of retained residue. 4. Naphthalene was primarily excreted unchanged (> 99% in freshwater-acclimated bass and > 88% in seawater-acclimated bass), but small amounts of 1,2-dihydro-1,2-dihydroxynaphthalene and 1- and/or 2-naphthylsulphate were formed.

Animals↗

Effects of diet and cold acclimation on lipid composition of rat interscapular brown adipose tissue.

The effects of diet and of cold acclimation on lipid composition of interscapular brown adipose tissue (BAT) were studied in rats. Three groups of animals were acclimated for 20 weeks to 28 degrees C (controls), 5 degrees C (CA) or to a daily fluctuating temperature (Cy). They received either normal fat (5 p. 100 lipids) [NF] or high fat (26 p. 100) [HF] diets. Cold acclimation increased the tissue weight and its protein, phospholipid, free fatty acid and cholesterol content. It decreased the total lipid proportion in the tissue. HF diet led to an increase in lipid content and to a decrease in the protein content only in control and Cy groups. The mean chain length of triglyceride or phospholipid fatty acids was increased by HF diet and cold acclimation. The proportion of unsaturated acids was not changed in cold acclimated rats, but the amount of arachidonic acid bound to phospholipid was significantly increased. It is concluded that the total amount of lipid in the diet acts on the synthesis of BAT lipids. The cold dependant changes in lipid composition which are similar but less important in cyclic cold acclimation than in constant cold adaptation seem to be proportional to the increase in the tissue energy metabolism.

Acclimatization↗

Changes in thyroid hormone and insulin status of the brown adipose tissue of cold acclimated rats on short term exposure to heat.

Acclimation of rats to cold caused 45% increase in the concentration of triidothyronine (T3) and 35% increase in the concentration of thyroxine (T4) in serum. Exposure of cold-acclimated rats to heat (12 hr, 37 degrees C) failed to decrease the concentrations of thyroid hormones in circulation. The concentration of T3 in brown adipose tissue (BAT) increased almost 10-fold on cold acclimation. Iodothyronine deiodinase activity also registered 3-fold increase. Exposure of cold-acclimated animals to heat caused decrease in the concentration of T3 in BAT without appreciably affecting T4 concentration. In liver tissue, the changes in hormone concentrations were quite small compared to those in BAT. On thyroidectomy or when fed with propyl thiouracil, rats could not survive exposure to the cold. The concentration of insulin in circulation showed small increase, while that in the tissues showed significant decrease on acclimation of rats to the cold. The concentration of the hormone in BAT registered significant increase on exposure of cold-acclimated animals to heat (12 hr, 37 degrees C). The increase in liver was marginal. The temperature-dependent response of T3 indicates an important role for this hormone in rapid physiological response in BAT.

Acclimatization↗

[Studies on adipocyte glucagon receptor assay--with special reference to the effect of cold acclimation on glucagon receptors of white adipocytes].

The changes in glucagon receptors of white adipocytes from cold-acclimated rats were investigated to know the metabolic role of glucagon in cold acclimation by establishing a glucagon radioreceptor assay system for isolated white adipocytes. Glucagon radioreceptor assay methodology The binding of 125I-labelled glucagon to isolated epididymal white adipocytes was linearly related to the number of cells (0.5-2.0 X 10(5) cells/ml) added in the medium. At a cell concentration higher than 3.0 X 10(5) cells/ml, the amount of specific binding failed to show the proportional relationship to the number of adipocytes. The effects of incubation temperature (4 degrees C, 25 degrees C and 37 degrees C) on the glucagon binding were investigated. Incubation at 25 degrees C was adopted in the present study because of the highest maximum binding and the longest steady state obtained. Preincubation at 25 degrees C for 15 min increased significantly the amount of specific binding. It was confirmed that bacitracin, polypeptide antibiotics, inhibited significantly the degradation of glucagon. The glucagon binding under these conditions was found to be saturable and reversible, validating a specific reaction for the glucagon receptor. When a Scatchard plot was constructed, the data was curvilinear with an upward concavity, indicating the presence of at least two classes of binding site with different fixed affinities or of negatively cooperative interactions between receptors. It was concluded that an appropriate condition for glucagon receptor assay of white adipocytes consists of cell concentration of 1 X 10(5) cells/ml, 15 minute-preincubation and 30 minute-reaction at 25 degrees C in the presence of bacitracin (1 mg/ml). Effect of cold acclimation on glucagon receptors of white adipocytes Cold acclimation decreased the size and increased the number of epididymal white adipocytes. Cold acclimation increased the number of glucagon receptors of white adipocytes; about 140% increase expressed as per cell, approximately 260% increase per unit of surface area and 210% increase per whole tissue. The affinity of binding sites was not changed. The increased binding sites could explain, at least partly, the enhanced metabolic response of cold-acclimated rats to glucagon.

Acclimatization↗

Structural studies of natural actomyosin from thermally acclimated frogs.

Natural actomyosin was isolated from skeletal muscle of frogs (Rana catesbeiana) acclimated at 25 degrees C and 5 degrees C. It was found that preparations isolated from warm-acclimated frogs may display considerable degradation of myosin heavy chains as compared with preparations isolated from cold-acclimated frogs. However, degradation may be minimized by inclusion of protease inhibitors during purification, indicating enhanced protease activity in preparations of natural actomyosin from warm-acclimated frogs. When purified in the presence of protease inhibitors, natural actomyosin from both warm-acclimated and cold-acclimated frogs exhibits comparable subunit composition of SDS-gel electrophoresis. The overall gel pattern is similar to that obtained from rabbit natural actomyosin except that in the frog, troponin-T and troponin-C appear to co-migrate with tropomyosin and myosin light chain 2, respectively.

Acclimatization↗

Effects of heat acclimation on atropine-impaired thermoregulation.

The effects of saline or atropine injection (2 mg, im) on eccrine sweating and performance time in seven healthy male subjects were evaluated during treadmill walking (1.34 m X s-1) in a hot-dry environment (Ta = 49 degrees C, Tdp = 20.5 degrees C) before and after heat acclimation (HA). Mean skin temperature (Tsk), rectal temperature (Tre), and heart rate (HR) were continuously measured. Sweat loss from the skin (Msw) was calculated by changes in body weight. HA resulted in decreased (p less than 0.05) Tre (0.4 degrees C) and HR (17 b X min-1), and increased (p less than 0.05) Msw (16 g X m-2 X h-1) during the saline experiments. Pre-acclimation, Msw was reduced (p less than 0.01) 65% (151 g X m-2 X h-1) with atropine, which resulted in higher (p less than 0.01) Tre (0.4 degrees C) and Tsk (2.8 degrees C). HR was increased 48% (53 b X min-1) by atropine pre-acclimation (p less than 0.01). Post-acclimation, atropine reduced (p less than 0.01) Msw 33% (100 g X m-2 X h-1) and increased (p less than 0.01) HR 63% (62 b X min-1) compared to saline exposures. The change in Tre X min-1 (delta Tre/delta t) was lower (p less than 0.05) in atropine-injected subjects following heat acclimation, and their worktime was improved by an average of 23.5 min (p = 0.08). These data demonstrate that heat acclimation improves the endurance time of atropine-treated subjects in a hot-dry environment. This improvement was, in part, due to the potentiation of sweat gland activity enabling greater evaporative cooling for the same dose of atropine.

Acclimatization↗

Acclimation to hypoxia increases survival time of zebrafish, Danio rerio, during lethal hypoxia.

Survivorship of zebrafish, Danio rerio, was measured during lethal hypoxic stress after pretreatment in water at either ambient oxygen or at a lowered, but nonlethal, level of oxygen. Acclimation to nonlethal hypoxia (pO(2) congruent with 15 Torr; ca. 10% air-saturation) for 48 hr significantly extended survival time during more severe hypoxia (pO(2) congruent with 8 Torr; ca. 5% air-saturation) compared to survival of individuals with no prior hypoxic exposure. The magnitude of the acclimation effect depended upon the sex of the fish: hypoxia pretreatment increased the survival times of males by a factor of approximately 9 and that of females by a factor of 3 relative to controls. In addition, survival time of control and hypoxia acclimated fish depended upon when in the year experiments were conducted. Survival times were 2-3 times longer when measured in the late fall or winter compared to survival times measured during the spring or summer. These results demonstrate a direct survival benefit of short-term acclimation to hypoxia in this genetically tractable fish. The fact that the acclimation effect depended upon the sex of the fish and the season during which experiments were conducted demonstrates that other genetic and/or environmental factors affect hypoxia tolerance in this species. J. Exp. Zool. 289:266-272, 2001.

Acclimatization↗

Effects of long-term temperature acclimation on thyroid hormone deiodinase function, plasma thyroid hormone levels, growth, and reproductive status of male Atlantic cod, Gadus morhua.

The recent collapse of the Northwestern Atlantic cod fisheries has coincided with a cooling of water temperatures. During this time the condition factor of cod has been poor. The objective of the present study was to determine the effects of long-term temperature acclimation on growth reproduction and thyroid function in laboratory held Atlantic cod (Gadus morhua). One of the key parameters used to assess thyroid function is the peripheral metabolism of L-thyroxine (T4) by microsomal deiodinase enzymes. Deiodinase function has not been described for gadid fish. T4 outer-ring deiodinating activity (apparent K(m) 1-2 nM) was confined primarily to liver. Its properties resembled those for hepatic T4ORD activity of other teleosts and the mammalian type II deiodinase. The T4ORD activity of cod liver exceeded that of salmonids and could explain the high plasma T3 levels (10-18 ng/ml), which were 2-5 times greater than T4 levels. T4 and T3 inner-ring deiodination was confined mainly to brain. In order to determine the effects of long-term temperature acclimation on cod, somatic growth, reproduction, and thyroidal status were assessed monthly in 400-900-g satiation-fed male Atlantic cod captured in June from the St. Lawrence Estuary and then acclimated from August to the following June under a natural photoperiod at 2-4 degrees C (LT) or 6-10 degrees C (HT). Reproductive status was determined from the gonadosomatic index (GSI), plasma testosterone (T) and 11-ketotestosterone (11-KT) levels, and the appearance of milt; thyroidal status was determined from plasma T4 and 3,5,3'-triiodo-L-thyronine (T3) levels and hepatic T4ORD activity to produce biologically active T3. Testis maturation (high levels of 1 and 11-KT, and milt release) occurred in April and May and was uninfluenced by acclimation temperature. LT cod grew more slowly than HT cod. Differences in body weight were particularly evident from December to February. In conclusion, (i) cod possess outer- and inner-ring deiodinase activities, predominating respectively in liver and brain, and with properties resembling those of other teleosts, (ii) T4ORD activity of liver is unusually high and may account for the high plasma T3 levels in this species, (iii) T4ORD activity tends to increase during periods of increased somatic growth, and (iv) chronic acclimation of male cod to 2-4 degrees C, as opposed to 6-10 degrees C, decreases somatic growth but does alter circulating levels of thyroid hormones and androgens and it does not change the time of sexual maturation.

Acclimatization↗

Brown adipose tissue and thermogenesis in hypophysectomized rats in relation to temperature acclimation.

The aim of this work was to test the role of pituitary dependent hormones in cold-induced non-shivering thermogenesis. In the 28 degrees C-acclimated rat, hypophysectomy inhibited body growth and led to an atrophy of thyroid and adrenals. In brown adipose tissue (BAT) some alterations were induced which are usually observed after cold acclimation of the animal: increase in relative weight, decreases in the relative amount of lipids, increases in the amounts of protein and DNA and modification of the proportions of several phospholipid fatty acids; moreover, basal lipolysis, in vitro, was enhanced to the same extent as that following cold acclimation of the normal rat. The in vivo stimulation by norepinephrine (NE) of O2 consumption (test for nonshivering thermogenesis) and of fatty acid release into blood were suppressed. Progressive cold acclimation of the hypophysectomized rats at 15 degrees C led to a hypertrophy of BAT to the same extent as in the sham-operated animals. The in vivo sensitivity to NE was partially restored. The results suggest that hypophysectomy does not suppress the ability to acclimate to moderate cold by means of BAT dependent non-shivering thermogenesis. However, the low ability to produce heat seems to indicate that pituitary or pituitary-dependent hormones are necessary to optimize the cold stimulation of brown fat thermogenesis.

Acclimatization↗

Changes in tension generation and ATPase activity in skinned muscle fibres of the carp following temperature acclimation.

Common carp (Cyprinus carpio L.) were acclimated to either 7 degrees C or 23 degrees C for 1-2 months. Skinned fibre preparations were isolated from the white myotomal muscle, and ATPase activity measured during maximal isometric contractions. At 7 degrees C, fibres from the cold acclimated fish were found to generate more force than those from warm acclimated fish (123.1 and 97.2kN m-2 respectively), and more "work" (force X time integral) was obtained for each ATP hydrolysed. ATP turnover per myosin head in fibres from cold-acclimated fish was lower than in fibres from warn-acclimated fish (1.85 and 2.84 ATP S1(-1) s-1).

Acclimatization↗