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PubMed1970

Effect of temperature acclimatization on the fatty acid composition of goldfish intestinal lipids.

1. The fatty acid composition of whole goldfish, whole-intestinal mucosa, intestinal mucosal membranes and individual phospholipids extracted from mucosal membranes were measured, fish adapted to different temperatures being used. 2. Alterations of the adaptation temperature did not noticeably affect the fatty acid composition of the whole-fish lipids, but there were marked changes in the fatty acids of lipids extracted from homogenates of goldfish intestinal mucosa. These changes were more pronounced in a membrane fraction prepared from these homogenates. Raising the adaptation temperature by 20 degrees C halved the percentage of C(20:1), C(20:4) and C(22:6) fatty acids and nearly doubled the percentage of C(18:0) and C(20:3) fatty acids recovered. 3. Choline phosphoglycerides constituted about one-half and ethanolamine phosphoglycerides about one-quarter of the total membrane phospholipids. 4. The fatty acids of choline and ethanolamine phosphoglycerides were more susceptible to temperature-dependent changes than were the phosphoglycerides of inositol or serine. 5. The increase in C(18:0) fatty acid that occurred in membranes of warm-adapted fish was greatest for ethanolamine phosphoglycerides, but increases also occurred in other phospholipid fractions and in membrane neutral lipids.

Acclimatization↗
PubMed1997

Capillary geometry in the soleus muscle of rats cold-acclimatized for 68 generations.

The effects of chronic cold exposure on soleus muscle capillarity were examined, particularly in terms of the distribution of arteriolar and venular capillaries and their capillary domain area (CDA) in adult rats exposed to cold for 68 generations (CG; n = 6). These parameters were compared with those obtained from control rats (CON; n = 5) and deacclimatized rats (DCG; n = 4), reared in thermoneutral temperature after being reared for 11 generations in cold. Morphometric data were obtained from muscle cross sections exposed to a double-staining method that stained the arteriolar and venular portions of capillaries blue and red, respectively. In CG, the capillary densities of arteriolar and venular capillaries were significantly greater than that of both CON and DCG (P < 0.05). The CDA of arteriolar, intermediate and venular portions in CG was significantly smaller by 15, 14 and 13%, respectively, than those of respective portions in CON (P < 0.05). Although CDA of arteriolar and venular capillary portions was also smaller in DCG than in CON, the degree of reduction was less in DCG than in CG. The succinate dehydrogenase activity of soleus muscle was significantly greater in CG than in both CON and DCG (P < 0.05). These results suggest that adaptive changes in the oxygen transport system, identified as an increase in the number of arteriolar capillaries and a reduction in the diffusion distance for oxygen, were observed in the soleus muscle after chronic cold exposure. These changes may improve the effective oxygen supply to muscle tissues and enable muscle tissues to promote thermogenesis in the cold atmosphere.

Acclimatization↗
PubMed1990

Aerobic performance at altitude: effects of acclimatization and hematocrit with reference to training.

The aim of the present investigation carried out on six members of the Swiss 1981 Mt. Lhotse Shar (8398 m) expedition was to assess the quantitative role of some of the determinants of VO2max at altitude. The loss of VO2max expected for the investigated altitude range was partially counterbalanced by the training undergone by the subjects during the approach to the base camp. delta VO2max was -18% instead of the expected 30%-35%. The VO2max value attained shortly after arrival at 5200 m was not significantly increased (38.4 +/- 4.4 SD vs 36.9 +/- 3.3 ml O2.kg-1.min-1) with a progressive rise of Hb from 16.4 +/- 0.8 to 18.2 +/- 1 g/100 ml of blood. Hemodilution, by oral administration of 2 liters of the isosmolar solution ISOSTAR, at 5200 m led to a 2.3% decrease of Hct and a 7.3% reduction of VO2max per kg of body weight. The product of heart rate times systolic arterial pressure ("double product") was somewhat (but not significantly) greater in hypoxia than in normoxia at all work loads. The maximum value for this product, however, was 10%-15% lower at 5200 than at 400 m. The increase of Hb from 15.1 +/- 0.7 to 17.1 +/- 1.6 g/100 ml of blood pre- to post-expedition was not accompanied by a significant increase of VO2max determined at 400 m either absolute or per kg of body weight.

Acclimatization↗
PubMed1998

Acclimatization strategies--preparing for exercise in the heat.

More than 200 years ago, in 1768, Lind in his monograph: "An assay on diseases incidental to Europeans in hot climate" pointed out that habituation to hot climates reduced the danger to health. Two centuries later, Lind and Bass in a classical study which was carried out under hot/dry climatic conditions (49 degrees C and 20% rh) demonstrated that the adaptation to heat may be described as the series of physiological adjustments that occur when a person who is accustomed of living in a cool environment is transferred to a hot climate. This adaptation is a process which is fully achieved after 10 to 14 days of exposure to heat, but two thirds or even 75% of the adaptation is obtained already within 5 days (1). According to this study improved tolerance to heat is related to typical physiological changes: heightened sweating response, lowered heart rate, and lowered rectal temperature during exercise in the heat.

Acclimatization↗
PubMed1995

Blood lactate concentration following exercise: effects of heat exposure and of active recovery in heat-acclimatized subjects.

The purpose of this study was to examine the effect of ambient heat on the decrease in blood lactate concentration ([LA]bl) during passive and during active recovery. Ten trained men performed six 1-min bouts of exercise at 100% VO2peak on a cycle ergometer, with 1-min rest between the bouts. Each subject exercised twice in thermoneutral (22 degrees C, 40% RH, TN), and twice in hot (35 degrees C, 30% RH, H) conditions. Exercise was followed by either 40 min of passive recovery (sitting) or by 20 min active recovery (cycling at 35% VO2peak) and 20 min passive recovery, named thereafter, 'active recovery'. Capillary blood lactate was measured before, 1 min after, and every 5 min during recovery. Heart rate (HR), rectal and skin temperatures (Tre, Tsk) were monitored continuously. VO2 was measured prior to exercise, during the last exercise bout, the first 10 min of recovery, and periodically thereafter. Post-exercise [LA]bl was similar in all treatments (13.5 +/- 1.8, 13.0 +/- 1.3, 14.8 +/- 4.1, 13.3 +/- 2.6 mmol.l-1 for TN-active, TN-passive, H-active and H-passive, respectively). [LA]bl was significantly lower during active, compared to passive recovery in both, TN and H conditions. Environmental heart did not independently affect [LA]bl during passive or active recovery. Exercise resulted in an elevation in Tre in all treatments, with a significantly higher Tre during active recovery in H compared to the other sessions. Likewise, no differences in HR and in VO2 were observed between H and TN conditions during active nor during passive recovery.(ABSTRACT TRUNCATED AT 250 WORDS)

Acclimatization↗
PubMed1994

Structural order of membranes and composition of phospholipids in fish brain cells during thermal acclimatization.

A comparison of the structural orders of membranes of a mixed brain-cell population isolated from Cyprinus carpio L. acclimated to either summer (23-25 degrees C) or winter (5 degrees C) revealed a high degree of compensation (80%) for temperature, as assayed by electron spin resonance spectroscopy. The cells rapidly forget their thermal history and adjust the physical properties of the membranes when shifted to the other extreme of temperature either in vivo or in vitro. Phospholipids separated from both types of animals exhibit only around 10% compensation. Arachidonic and docosahexaenoic acids are the major polyunsaturated fatty acids in the brains, but the fatty acid composition of the brain total phospholipids does not vary with adaptation to temperature. Separation of phosphatidylcholines and phosphatidylethanolamines into molecular species revealed a 2- to 3-fold accumulation of 18:1/22:6, 18:1/20:4, and 18:1/18:1 species in the latter; 18:0/22:6 showed an opposite tendency. Molecular species composition of phosphatidylcholines did not vary with the temperature. The same trends of changes were seen with brains of freshwater fish from subtropical (Catla catla L.) or boreal (Acerina cernua) regions. It is concluded that the gross amount of docosahexaenoic acid (22:6) plays only a minor role in adjusting the membrane physical properties to temperature. Factors other than lipids might be involved in the adaptation processes. Due to their specific molecular architecture, molecules such as 18:1/22:6, 18:1/20:4, or 18:1/18:1 phosphatidylethanolamine might prevent the contraction of membranes in the cold and may provide an environment for some other components involved in the temperature regulation of physical properties of nerve cell membranes.

Acclimatization↗
PubMed2000

Acclimatization to altitude and normoxic training improve 400-m running performance at sea level.

To investigate the benefits of 'living high and training low' on anaerobic performance at sea level, eight 400-m runners lived for 10 days in normobaric hypoxia in an altitude house (oxygen content = 15.8%) and trained outdoors in ambient normoxia at sea level. A maximal anaerobic running test and 400-m race were performed before and within 1 week of living in the altitude house to determine the maximum speed and the speeds at different submaximal blood lactate concentrations (3, 5, 7, 10 and 13 mmol x l(-1)) and 400-m race time. At the same time, ten 400-m runners lived and trained at sea level and were subjected to identical test procedures. Multivariate analysis of variance indicated that the altitude house group but not the sea-level group improved their 400-m race time during the experimental period (P < 0.05). The speeds at blood lactate concentrations of 5-13 mmol x l(-1) tended to increase in the altitude house group but the response was significant only at 5 and 7 mmol x l(-1) (P < 0.05). Furthermore, resting blood pH was increased in six of the eight altitude house athletes from 0.003 to 0.067 pH unit (P < 0.05). The results of this study demonstrate improved 400-m performance after 10 days of living in normobaric hypoxia and training at sea level. Furthermore, the present study provides evidence that changes in the acid-base balance and lactate metabolism might be responsible for the improvement in sprint performance.

Acclimatization↗