In order to have a general view of metabolic requirements during swimming, in vitro aerobic and anaerobic fluxes were measured in red and white muscles from silver eels and yellow eels which differ in activity levels and nutritional states. These measurements were performed in control eels and after a 4 day swimming session (70% U(crit) in yellow eels, 80% U(crit) in silver eels). A swimming session significantly increases U(crit) from 12% to 18%, depending on the stage, with a significantly higher in vitro energy cost during the yellow stage at the muscle level. In vitro, the swimming session brings about a gain in anaerobic capacities rather than in aerobic ones. Some in vivo hypotheses are proposed.

This paper deals with the effects of exercise training on oxygen consumption (MO(2)) and ROS metabolism in the red muscle of trained and untrained female silver eels. Their critical swimming speed (U(crit)) was determined before and after a 4-day training (10h of swimming at 70% of U(crit) and 14 h at 50%, every day). The U(crit) of trained eels increased significantly (by about 7%). The in vitro MO(2) and ROS production by the red fibres were higher (not significant) in trained than in untrained eels, but the ROS production/MO(2) ratio was alike in both groups. The antioxidant-enzyme activities and lipoperoxidation index in trained eels were both lower than those of the untrained ones. These biochemical changes related to the increase in U(crit) suggest that such a training session could maintained or even increased aerobic power of the red muscle without deleterious impact by ROS. These regulations could play a role in the eel's swimming performance efficiency.

Mitochondrion is the main production site for reactive oxygen species (ROS). In endotherms, the existence of a positive relationship between ROS production and metabolic rate is acknowledged. But, little is known about ectotherms, especially fish, with a metabolic rate dependent on the environmental temperature. The maximal oxygen consumption and the production of highly reactive hydroxyl radicals by permeabilized red muscles of yellow and silver eels and trouts were measured concomitantly and compared to those of rats chosen for their comparable body mass, but different metabolic rate. The positive correlation found in fish between the metabolic rate and the ROS production showed a shift with respect to mammals.

Silver European eels (Anguilla anguilla L.) need to develop important aerobic capacities to cope with their long fasting spawning migration at depth, particularly males which are about half the size of females. Moreover, they have to face potential oxidative stress because reactive oxygen species (ROS) production is linked to the increase in metabolic rate. Thus, aerobic metabolism was globally evaluated in male and female silver eels exposed to a 10.1 MPa hydrostatic pressure (1,000 m depth). Oxygen consumption (MO2), ROS production and antioxidant enzyme activities were measured in the muscle fibres. Males showed a trend in both higher rate of aerobic metabolism and ROS production than females. After pressure exposure, ROS production was inversely correlated to metabolic rate only in males. By facilitating MO2 rise with no harmful effects by ROS, the supposed enhanced aerobic capacities of males could speed up the sustained swimming. In females, the tendency to lower metabolic rate and higher catalase activity would make them less vulnerable to ROS effects. These results are in agreement with the hypothesis for different migration depths between genders.

The diversity of fish is larger than for any other vertebrate group. There are more fish species than of all the other vertebrates together. Fish also inhabit more diverse habitats than any other group of vertebrates, from Himalayan or Andean brooks at 4,000 meters to abyssal depths of at least 8,370 m, thus spanning an extremely wide range of hydrostatic pressures. In studying the effects of hydrostatic pressure on biological systems it is fundamental to experimentally dissociate those effects from those of other factors, though these interactions could be of obvious interest. Particularly difficult, at all levels of biological organization, is the distinction between hydrostatic pressure effects per se and increased gas partial pressures effects. As P. Sebert and A. G. Macdonald pointed out, it is a curious fact that few marine biologists in general, and fish biologists in particular, have responded to the extraordinary range of interesting hyperbaric phenomena which fish present.

This review will focus on the effects of hydrostatic pressure on the oxidative metabolism and on the energy production of the eel Anguilla anguilla, in comparison with the results of investigations conducted on the other powerful euryhaline species, the chinese crab Eriocheir sinensis. Anguilla and Eriocheir were chosen as being both aquatic ectotherms with comparable life modes, the eel being however "preadapted" to high pressure while the crab normally never encounters high levels of pressure during its life cycle. Comparison between both species should lead to better knowledge of the biological effects of hydrostatic pressure per se.Experimental evidence suggests that the oxygen consumption ṀO2 decrease observed in both animal species during exposure to 101 ATA hydrostatic pressure and which follows a transient increase, likely results from a decrease in O2 use at the cell level. That idea of an alteration of aerobic metabolism during the first hours under pressure is substantiated by a set of experiments on the eel. However, results indicate that, after some days under pressure, the shallow water fish is quite able to acclimate perfectly to high pressure. The hypothesis that pressure induces a state resembling histotoxic hypoxia during the first hours of exposure is put forward and discussed.The second part of the review focuses on some results showing that osmoregulation is also concerned with hydrostatic pressure. Results obtained on the freshwater eel clearly establish the occurrence of a Na+ balance impairment at the tissue level induced by a long-term (30 days) exposure to pressure. It is interesting to point out that this impairment occurs at the same time when a new state of energetic metabolism results from adjustments of intertissue coupling of anaerobic and aerobic metabolisms induced by pressure. It is shown that the physiological processes involved in the control of the hydromineral balance in the chinese crab (which never experiences high-pressure exposure in the course of its life cycle) are outstandingly resistant to pressure by comparison with other crustaceans like the crayfish and the shore crab. Disturbances in hydromineral balance and energetic metabolism in the chinese crab are rapidly resorbed and adjusted to a new state of activity.

To reproduce, European eels must undergo a long migration without feeding. During this migration they have to cope with many environmental factor changes, one of them being hydrostatic pressure. We focus on the effects of hydrostatic pressure on swimming energetics: does the pressure exposure modify swimming efficiency? By using a specially designed Blazka type swimming tunnel able to work under pressure, we have measured oxygen consumption of migrating male silver eels at different swimming speeds (from 0.2 to 1.0BL/s) first at atmospheric pressure then at 101 ATA hydrostatic pressure. The results show that pressure increases the energetic swimming efficiency by decreasing oxygen consumption for a given swimming speed. Such a pressure effect could represent a remarkable adaptation enabling eels to spare their energy stores and swim for a long time.

European silver eels migrate 6000 km to their supposed spawning area in the Sargasso sea. As the eel is fasting, this intense swimming activity is realised only with fat stores, involving mainly red muscle i.e. aerobic metabolism. However, eel migration is performed at depth and thus in cold water, both being known to induce changes in muscle energy metabolism. During migration, white and red muscles can operate together or separately in order to counteract the eventual effects of low temperatures and/or high pressures. We have studied the temperature sensitivity (5,15, and 25 degrees C) of aerobic and anaerobic metabolism in both sexes. At the same temperature, migrating eels have a higher basal glycolytic flux. Moreover, there are temperature and sex effects: anaerobic glycolysis (JB) is more sensitive to cold water whereas aerobic (JA) is more affected by warm. Males, which are less sensitive to cold water, also have higher aerobic fluxes than females. As depth corresponds to low temperature, the possibility that males migrate more deeply than females is discussed. In an ecophysiological context, it is interesting to suppose that males and female eels migrate at different depths in order to optimize their energy utilization by aerobic and / or anaerobic pathways. (C) 2008 Elsevier Inc. All rights reserved.

During their migration for reproduction, European eels have to cope with many environmental factors changes. The main changes concern hydrostatic pressure and temperature that are important environmental and physiological factors when considering life in the deep sea. We focus on the consequences of pressure (from 0.1 to 12.1MPa by 1MPa steps) and temperature (9, 15, 22°C) shifts on the oxygen consumption (MO2) at the whole animal level. Because of their morphological differences, we are also interested in males and females to evaluate the best conditions for migration. Firstly, whatever temperature, males present higher aerobic capacities than females at atmospheric pressure. Secondly, an increase in temperature increases the pressure effects in males (synergy) but decreases them in females (opposite effects). We raise the hypothesis that two different migration strategies could be used in the water column in order to reach the breeding area: males could tend to privilege pressure and cold waters (deep water) and females, on the other hand, could opt for warmer temperature surface waters.

European silver eels are thought to undergo sexual maturation during their oceanic reproductive migration from the European continent to their spawning area in the Sargasso Sea. Tracking data and various anatomical and physiological features suggest that silver eels migrate in deep sea, leading us to hypothesise that high hydrostatic pressure (HP) influences the induction of eel reproduction. We subjected female and male silver eels to 101ATA for 3 and 7 weeks, respectively, in a hyperbaric chamber equipped with a freshwater recirculation system. In comparison with control eels kept at 1 ATA, HP effects were tested against the messenger RNA levels of pituitary gonadotropins (LHbeta, FSHbeta) using quantitative real-time RT-PCR. The effects of HP on gonadal activity were estimated by measuring gonadosomatic index, oocyte diameter and plasma levels of vitellogenin (Vtg) and sex steroids (E(2), 11-KT). At the pituitary level, LHbeta expression tended to increase while FSHbeta expression decreased in both sex, leading to an increase in the LHbeta/FSHbeta ratio. This suggests a differential effect of HP on the expression of the two gonadotropins. In females submitted to HP, we observed a significant increase in oocyte diameter and plasma levels of 11-KT and E(2). A similar trend was observed for 11-KT plasma levels in males. In females, Vtg plasma levels also significantly increased, reflecting the stimulatory effect of sex steroids on hepatic vitellogenesis. Our results suggest that HP plays a specific and positive role in eel reproduction but additional environmental and internal factors are necessary to ensure complete sexual maturation.

Hitherto, the question of the energetic cost of osmo-ionoregulation in euryhaline crustaceans has received only cursory attention. Many studies are scanty, even contradictory. Most of the experiments carried out on this topic are based on measurements of oxygen consumption and estimates of aerobic metabolic activity. The ATP content of crustacean tissues has also sometimes been measured. Some attempts were made to correlate osmoregulation patterns, ions transport activity and oxygen consumption of some decapod crustacea. The basic aim of this work is to re-examine the question with some new data.