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HYPOTHESIS AND THEORY article

Front. Physiol., 13 June 2012
Sec. Aquatic Physiology
This article is part of the Research Topic The physiological consequences of breath-hold diving in marine mammals; the Scholander legacy View all 13 articles

Fatty acid use in diving mammals: more than merely fuel

  • 1 Department of Biology, Baylor University, Waco, TA, USA
  • 2 Department of Biology, Colorado State University, Ft. Collins, CO, USA

Diving mammals, are under extreme pressure to conserve oxygen as well as produce adequate energy through aerobic pathways during breath-hold diving. Typically a major source of energy, lipids participate in structural and regulatory roles and have an important influence on the physiological functions of an organism. At the stoichiometric level, the metabolism of polyunsaturated fatty acids (PUFAs) utilizes less oxygen than metabolizing either monounsaturated fatty acids or saturated fatty acids (SFAs) and yields fewer ATP per same length fatty acid. However, there is evidence that indicates the cellular metabolic rate is directly correlated to the lipid composition of the membranes such that the greater the PUFA concentration in the membranes the greater the metabolic rate. These findings appear to be incompatible with diving mammals that ingest and metabolize high levels of unsaturated fatty acids while relying on stored oxygen. Growing evidence from birds to mammals including recent evidence in Weddell seals also indicates that at the whole animal level the utilization of PUFAs to fuel their metabolism actually conserves oxygen. In this paper, we make an initial attempt to ascertain the beneficial adaptations or limitations of lipids constituents and potential trade-offs in diving mammals. We discuss how changes in Antarctic climate are predicted to have numerous different environmental effects; such potential shifts in the availability of certain prey species or even changes in the lipid composition (increased SFA) of numerous fish species with increasing water temperatures and how this may impact the diving ability of Weddell seals.

Introduction

Diving mammals, such as the Weddell seal (Leptonychotes weddellii), are under extreme pressure to conserve oxygen as well as produce adequate energy through aerobic pathways during breath-hold diving. It is recognized that diving mammals undergo a dive response involving apnea (cessation of breathing), bradycardia, and subsequent decreased cardiac output, as well as peripheral vasoconstriction (reduced blood flow or ischemic conditions in the working skeletal muscles) causing the animal to depend solely on a finite supply of oxygen stored internally. In other words, when diving mammals are active (foraging), they are holding their breath, their working muscles receive little to no blood flow, and they rely solely on internal stores of oxygen, to fuel, and sustain a lipid based aerobic metabolism. Therefore, dive duration can be directly correlated to the rate of oxygen utilization and any factors that affect the rate of oxygen consumption could alter dive times (Fahlman et al., 2008; du Dot et al., 2009; Williams et al., 2011; Shiomi et al., 2012).

While dependant on lipid and protein from a typically piscivorous prey source, lipids provide double the energy per mass when compared to protein and are important as a stored energy source as well as for thermoregulation and hydrodynamics (Castellini et al., 2009). More detailed use of lipids reveal a possible developmental role as well as preferential mobilization of specific fatty acids during lactation (Wheatley et al., 2008; Trumble et al., 2010). Trumble et al. (2010) reported that the primarily ice-based Weddell seal pup had increased polyunsaturated fatty acids (PUFAs) recovered from lipids associated with their skeletal muscle whereas saturated fatty acids (SFAs) were decreased when compared with adults. Assuming similar lipid consumption between age classes, these findings led to speculation that pups were metabolizing SFAs in greater amounts than the adult age class. While consuming a milk high in unsaturated fatty acids (UFA; Wheatley et al., 2008), it was hypothesized that these young seals increased their metabolic and energetic advantage (increased oxygen to metabolize SFA when compared to UFA and more energy per mass) to combat their high mass-specific heat loss and metabolic limitations of being an endothermic mammal in Antarctica. As these seals continued to mature to adults, the fatty acids recovered were primarily monounsaturated fatty acids (MUFAs), however, there appeared to be an exchange between SFA and PUFA between these age classes (Trumble et al., 2010). In this paper, we explain the stoichiometry associated with fatty acid metabolism and hypothesize on the advantages and disadvantages of these fatty acid groups, primarily PUFAs, in diving mammals inhabiting polar waters. Finally, we offer some speculation on potential disadvantages of metabolizing certain groups of fatty acids in a changing environment.

Oxygen and Diving

The important role for the rate of oxygen consumption and diving was recently elucidated in emperor penguins (Aptenodytes forsteri; Shiomi et al., 2012). The results of this study indicated that once a certain amounts of work or numbers of flipper strokes were reached, the animals initiated their return to the surface regardless of the amount of time spent diving. To date, this is the strongest evidence that alteration in oxygen consumption or work effort significantly alter dive times. Along with the aforementioned emperor penguins, Weddell seals represent extreme examples of this breath-hold model. These divers routinely dive under an ice ceiling, which offers less than 5% access to breathable surface area (Figure 1). This is in sharp contrast to open water divers such as elephant seals (Mirounga angustirostris) or other non-polar pinnieds. These constraints demand that the Antarctic divers be more tightly regulated with respect to their oxygen utilization; they must complete a dive cycle and find a breathing hole before their oxygen stores are depleted. Previous research has illustrated how these and open water divers are uniquely adapted to their environment and how energy is conserved even at the molecular level (Burns, 1996; Burns et al., 1998; Kanatous et al., 1999, 2001, 2002, 2008a,b; Burns et al., 2005, 2007; Clark et al., 2006, 2007; Noren et al., 2008b; Ptitsyn et al., 2010; Trumble et al., 2010; Ponganis et al., 2011; Williams et al., 2011). For example, studies of adult Weddell seals, harbor seals (Phoca vitulina) and Steller sea lions (Euematopias jubatus) have revealed that their muscle adaptations to maintain a lipid based aerobic metabolism under the hypoxic conditions associated with breath-hold diving include: (1) an increased aerobic capacity (or one that is matched to routine levels of exertion), (2) a reliance on fatty acid catabolism for aerobic ATP production, (3) enhanced oxygen storage and diffusion capacity, and (4) a reduced dependency on blood-borne oxygen and metabolites (e.g., decreased capillary density) compared to terrestrial mammals (Davis et al., 1991; Davis and Kanatous, 1999; Kanatous et al., 1999, 2001, 2002). Recently, physiological studies have begun to describe the development of diving capacity and oxygen stores in diving mammals (Noren et al., 2004, 2005, 2006, 2008a; Clark et al., 2006, 2007; Kanatous et al., 2008a). Recent data have reported numerous physiological changes such as an increase in the concentration of myoglobin to levels ∼60% of those found in adults. These adaptations occur during weaning periods and are necessary for these animals to initiate independent foraging (Burns, 1996; Kanatous et al., 2008a).

FIGURE 1
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Figure 1. Weddell seals routinely feed on a diet of Antarctic silverfish (Pleuragramma antarcticum) that is rich in unsaturated fatty acids. Recent data indicates that similar to long distance migratory birds, adult Weddell seals preferentially metabolize PUFAs in contrast to either monounsaturated or saturated fatty acids (Trumble et al., 2010).

In terms of skeletal muscle development, the cessation of weaning and commencement of diving in Weddell seals induces developmental changes in muscle physiology that parallel changes in activity. Preliminary microarray results indicate differential expression of RNA transcripts associated with various ontogenic signaling pathways, in addition to differences in transcripts associated with lipid metabolism, among age classes (Kanatous et al., 2008b; Ptitsyn et al., 2010). These previous findings mirrored results describing significant changes in the lipid composition and potential utilization of fatty acids in skeletal muscle during these developmental stages (Trumble et al., 2010). In addition, where this developmental trend of increasing exercise capacity occurs from birth in terrestrial mammals, we found that the skeletal muscle physiology of Weddell seal pups suggests a higher capacity for exercise than juveniles or adults. This is indicated by pups having the highest percentage of type I slow oxidative fibers as well as the highest mitochondrial volume densities of any age class. A relative lack of an increase in aerobic enzymes, however, indicates that these results may be due to an adaptation for enhanced non-shivering thermogenesis (Kanatous et al., 2008a). Furthermore, juveniles were recently shown to have the highest expression of myoglobin (72.4 ± 7 vs. 55.9 ± 2.5 and 35.5 ± 3 mg g−1 wet mass muscle in adults and pups, respectively) supporting the hypothesis that myoglobin concentrations differ with behavioral differences in diving activity (Kanatous et al., 2008a).

Fatty Acids and Stoichiometry

Typically known as a major source of energy, lipids also participate in structural and regulatory roles that have an important influence on the physiological functions of an organism. As essential fatty acids, it is well known that PUFAs of n−3 and n−6 groups are considered the most powerful intracellular and intercellular mediators and modulators of the cell signaling network and cell membrane fluidity (important in polar habitats). The action of PUFAs has been shown to have various effects on immune and inflammatory processes (Puertollano et al., 2004). While the processes above are certainly important for a developing diving mammal, fatty acids play a large role in fueling metabolism and may provide insight into diving adaptations. For mammalian diver’s it is imperative to conserve oxygen to maximize success of an intake of primarily unsaturated fats and proteins. This intake of UFAs and subsequent transport and oxidation within skeletal muscles (assuming skeletal muscle activity during diving) may to be an advantage to the diver. Specifically, the moles of oxygen needed to metabolize any particular SFA are slightly greater than that for a similar length UFA (MUFA and PUFA). This stoichiometry of oxygen consumption is based on the number of double bonds and thus hydrogen involved (see below for example). If extrapolated to the fatty acid groups (not the individual fatty acids) identified in Weddell seal blubber (14–24 carbon; Trumble et al., 2010), the mean moles of oxygen needed to oxidize PUFAs (29 mol O2/FA) is greater than MUFAs (26 mol O2/FA) and SFAs (23 mol O2/FA). Upon closer examination, a majority of saturated and unsaturated fatty acids recovered (percent of total) from the blubber (Wheatley et al., 2008) and muscle of Weddell seals are 18 carbons (18C) in length (>50%, Trumble et al., 2010). Specifically, an 18C SFA containing 36 hydrogen atoms requires (36/4) + 18 − 1 = 26 mol of oxygen for complete oxidation whereas the most commonly recovered MUFA, 18:1, requires 25.5 mol and the most commonly recovered PUFA, 18:3 requires 25 mol of oxygen for complete oxidation. Based on mean percent fatty acid composition from Weddell seal pups (SFA, 28%; UFA, 72%), juveniles (SFA, 31%; UFA, 69%), and adults (SFA, 30%; UFA 70%; Trumble et al., 2010) and an estimated mean total percent blubber mass for each age class (Gales and Burton, 1987; Noren et al., 2008b; pups, 32 ± 0.8%; juveniles, 21.5 ± 0.7%; and adults, 23.9 ± 0.7%) estimates of moles of oxygen required to oxidize saturated and unsaturated fatty acids can be calculated (Figure 2). This may equate to UFA-oxygen conservation when compared with metabolizing similar amounts of SFAs in Weddell seal adults. While this alteration of oxygen consumption appears insignificant in terms of oxygen moles oxidized between these 18C fatty acids, when extrapolating to a 400-kg adult (35% muscle mass; Ponganis et al., 1993) and differences in mass-specific metabolic rates (0.676 Mb0.75/kg; Kleiber, 1975) metabolizing an unsaturated 18C fatty acid offers an increase of ∼30 s of dive time (not taking activity budget into account) during a 30-min dive. A dive time shortened by 30 s (assuming dive locomotion at 1–3 m/s), would shortened the distance covered by 30–90 m, which could significantly alter foraging or breathing hole location success.

FIGURE 2
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Figure 2. Estimated moles of oxygen needed to completely oxidize saturated (SFA), and unsaturated (UFA) fatty acids recovered from Weddell seal skeletal muscles (n = 20) in 2006. Calculations derived from mean moles of oxygen (see text) and mean lipid amounts in skeletal muscle (Trumble et al., 2010) among age groups and mean mass of age groups (estimates for blubber mass derived from Noren et al., 2008b) and mean total percent of fatty acids recovered. note: fatty acids include (SFA; C14:0–24:0), monounsaturated (MUFA; 14:1n−5, 16:1n−9, 16:1n−7, 18:1n−9, 18:1n−7, 18:1n−11, 20:1n−9, 20:1n−7, 22:1n−11, 22:1n−9, 24:1n−9), and polyunsaturated (PUFA; 18:2n−6, 18:3n−6, 18:3n−3, 18:4n−3, 20:2n−9, 20:2n−6, 20:3n−6, 20:4n−6, 20:3n−3, 20:4n−3, 20:5n−3, 22:4n−6, 22:5n−6, 22:5n−3, 22:6n−3).

The stoichiometric relationship between saturated and unsaturated fatty acids from an energy production (ATP) perspective also results in differences, which may also influence diving. Using the most common fatty acid recovered (18:1, Trumble et al., 2010), we surmise that the oxidation of unsaturated fatty acids requires additional auxiliary enzymes (isomerases and a reductase). This becomes important in that the double bonds formed in beta-oxidation are trans as opposed to cis in naturally occurring unsaturated fatty acids. Specifically, an isomerase is required for breaking the double bond in MUFAs, which are typically between carbons 9 and 10. Thus, oleate (18:1) requires three cycles of beta-oxidation with each cycle removing two carbons, replacing the double bond at the number 3 position. The hydratase of beta-oxidation requires the double bond to be in the trans configuration and at second carbon location. Therefore, the ATP count for MUFAs (>50% of total percent of FAs recovered) is two less than the fully saturated analog because one fewer FADH2 is generated (for 18:0, there are 146 ATP produced; for 18:1 there would be 144 ATP produced). Further, to process the second double bond in a PUFA, for example 18:2, another reductase and isomerase are required. Since the double bonds are typically in the 9 and 12 positions, the three cycles of beta-oxidation can proceed as usual, resulting in the double bonds at the 3 and 6 positions. Beta-oxidation will then proceed to form a trans-2, cis-4 product. The mammalian version of the second auxiliary enzyme, another reductase, reduces this to a singly unsaturated product with a trans double bond in the 3 position. With this additional reductase involved, the ATP count will be three fewer than for a fully saturated version because, in addition to the loss of FADH2, one NADPH is used for this additional reductase. Thus, the ATP count for a fatty acid configured as 18:2 would only be 141 as compare to 146 from a saturated 18C fatty acid. While there may be a loss in ATP production by preferentially metabolizing UFAs as compared to SFAs, dives are more limited by oxygen than ATP thus the oxygen conservation may dramatically outweigh the differences in ATP production for these animals.

The Fatty Acid Trade-Off: Membrane Composition

The consumption of a high fat diet produces a surplus of NADH and FADH2, which subsequently increases the generation of reactive oxygen species (ROS). Indeed, a high fat diet has been shown to increase the rate of H2O2 (ROS species) production in skeletal muscle mitochondria (Nadal-Casellas et al., 2010). This production of ROS has been reported to contribute to the processes of aging as well as progression of numerous disorders such as Type II diabetes and Parkinson disease in mammals (Kang and Hamasaki, 2003). Ultimately, the increased rate of ROS production by the mitochondria results in mitochondrial dysfunction in skeletal muscle. However, recent studies have begun to elucidate the differential role of cellular membrane lipid composition in the susceptibility to ROS damage (Hulbert, 2008a,b, 2010; Montgomery et al., 2011). These studies have shown that membranes composed of higher concentrations of PUFAs have an increased susceptibility to ROS damage by lipid peroxidation, which ultimately shortens lifespan in animals. However, it has been speculated that membranes higher in MUFAs protect against ROS damage (Hulbert, 2010). Trumble et al. (2010) reported that greater than half of all the recovered fatty acids associated with the skeletal muscle of Weddell seals were MUFAs. We speculate this increase in MUFA levels supports in ameliorating damage by ROS. New research also found that membranes of the relatively long-lived short-beaked echidna (Tachyglossus aculeatus) are more monounsaturated and less polyunsaturated than would be predicted from their body size which were hypothesized to ameliorate ROS damage and promote long life spans (Hulbert, 2008a,b, 2010). This association between PUFA membrane levels appears to be related to life span (Hulbert, 2010) as well as Basal metabolic rate (BMR) and appears to hold true for most terrestrial mammals and birds studied (Hulbert, 2008a,b, 2010).

Basal metabolic rate represents cellular living at a minimal cost within certain assumptions such that the mass-specific BMR has been shown to vary among species inversely related to body size. An idea proposed and developed by Hulbert and Else (1999) suggests that this variation in BMR is not only a function of body size but also directly related to cellular metabolic rate which is directly correlated to the lipid composition of the membranes (Hulbert and Else, 1999). Further, and mentioned above, there appears to be a direct positive correlation between PUFA levels in the membrane and a higher BMR. We report here for the first time, that Weddell seals appear to follow the concept proposed by Hulbert and Else (1999); PUFAs are increased in the skeletal muscle membrane of the smaller pup and decline with the larger animals (Figure 3). While unknown whether this switch in membrane fatty acids occurs during development in terrestrial mammals, we report that this metabolic switch in membrane composition occurs after pupping or lactation and seems to be transitioned in juveniles. In terrestrial mammals, higher levels of PUFAs have been reported in the membranes of relatively smaller mammals and have been associated with leakier membranes and more active pumps (Hulbert, 2010). This “PUFA-permeable prefigure” may add evidence to our recent findings that Weddell seal pups offset their thermal challenge of being an endothermic animals born into an extremely harsh environment of Antarctica through the use of increased and potentially uncoupled metabolism. In short, it appears that non-diving pups adopt the metabolic and cellular “benefits” of the relatively small terrestrial mammal PUFA rich membrane composition. At this time, we do not know the mechanisms involved with this membrane switch. However, it appears to coincide with development, or the physiological shift to adult divers. Further, as membrane PUFA levels change, MUFA and SFA levels increase in adult membrane composition for possible additional protection from ROS damage from proportionally high rates of sustained lipid metabolism and from the reperfusion of the muscles associated with the end of dives (Figure 3).

FIGURE 3
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Figure 3. Membrane (phospholipids) fatty acids (saturated, SFA; monounsaturated, MUFA; and polyunsaturated, PUFA) in Weddell seal skeletal muscle (pup, n = 5; juvenile, n = 5; adult, n = 5). Differences in lower case letters denotes statistical differences among age classes (p < 0.05).

Interestingly, an additional “benefit” or adaptation of ingesting and metabolizing PUFAs, especially in adult diving mammals, may be its influence on heart rate. A report by Gudbjarnason et al. (1978) reported that the heart rate of animals, ranging from mice to whales, was directly related to the levels of 22:6n−3 in their cardiac phospholipids (Gudbjarnason et al., 1978). Subsequently, it was determined that this increase in 22:6n−3 was also positively correlated with increased Ca2+ATPase activity in the cell (Infante, 1987) which led to the “membrane pacemaker theory” mentioned above (Hulbert and Else, 1999). This notion that heart rate is influenced by n−3 fatty acids has been pursued by several investigators with the general consensus that ingestion of n−3 fatty acids tend to lower resting heart rates (Christensen et al., 1999; Billman and Harris, 2011). Assuming that the relatively lower PUFA levels associated in the skeletal muscle lipids is a function of increased metabolizing of PUFAs and not a function of decreased PUFA intake, then our findings may indicate a preferential fatty acid adaptation to lower heart rate during diving. It should be mentioned that PUFAs cannot be formed de novo by mammalian cells and therefore must be obtained from the diet. Assuming a PUFA rich prey equal in proportion to what is found in milk (Wheatley et al., 2008) then our findings suggest PUFAs were preferentially mobilized by the muscle for energy and, more importantly, switch in levels in the skeletal muscle membranes. At this time, we can only speculate that this switch may suggest a regulation of desaturases or elongases associated with membrane lipid constituents. Further research is needed to confirm this hypothesis.

It has been reported that long distance migratory birds (Calidris pusilla) ingest a diet high in n−3 PUFA prior to migration, potentially acting as a molecular signal to prime flight muscles and increase oxygen efficiency while using less energy (Maillet and Weber, 2006; Piersma, 2011). Several studies contribute to this notion and suggest that PUFAs may affect the performance of skeletal muscles and locomotion in a variety of vertebrates (McKenzie et al., 1998; Helge et al., 2001; Infante et al., 2001; Valencak et al., 2003). We speculate PUFAs, especially n−3’s, play an important role in the development of foraging from pup to adults and that these fatty acids may be functionally related to oxygen conservation, locomotor performance, life stage specific energetic demands and diving ability. In a recent study involving rats switched from a SFA diet to fish oil (high n−3 PUFAs) myocardial oxygen consumption, coronary flow and percent oxygen extraction was significantly reduced while maintaining integrity of contractile function in the heart muscle (Pepe and McLennan, 2007). The metabolic costs of foraging are critical components of the energy budget of animals and will have direct affect on the amount of prey they must obtain to survive. This is especially true for breath-hold deep divers; where any increases in the metabolic costs will significantly alter their dive times and foraging success. As stated above, our recent data indicates that similar to long distance migratory birds, adult Weddell seals preferentially metabolize oxygen-conserving PUFAs in contrast to either MUFAs or SFAs, which enable the seals to preserve their limited oxygen resources during diving. An important area of future research will be elucidating the molecular controls that regulate this switch in metabolic fuel during ontogeny.

Fatty Acids as Regulatory Signals

Because myoglobin has been shown to increase during the weaning period of both penguins and seals before they initiate diving (Burns et al., 2005, 2007; Clark et al., 2007) the potential for myoglobins regulation to be dependent on its interplay with specific fatty acids seems plausible. Indeed, recent evidence has shown that the amount and type of lipids act as important initial regulators of myoglobin in diving mammals (De Miranda Jr. et al., 2012) with some indication of secondary regulation by activity level and calcium signaling (Kanatous et al., 2008b, 2009; Ptitsyn et al., 2010). In comparative animal studies, an increase of n−3 PUFAs or a high n−3 to n−6 ratio of fatty acids was shown to prompt increases in calcium transport and calcium absorption in PUFA-deficient rats (Kruger and Horrobin, 1997; Weiss et al., 2005). It has been established in terrestrial animals and diving mammals that calcium signaling, as well as its downstream targets of calcineurin and NFAT, plays an important role in determining fiber type distribution, aerobic capacity and myoglobin concentrations in skeletal muscles (Chin et al., 1998; Spangenburg and Booth, 2003). Recent evidence from our labs indicates this increase of myoglobin expression in weaning animals before they start diving may be initiated through an activity and calcium independent pathway. While further studies in cell culture may yield a more specific response to certain fatty acids, our current research strongly suggests that the pre-dive increases in myoglobin of divers during weaning may be associated with changes in the lipid composition of the milk associated with nursing (De Miranda Jr. et al., 2012). Additional results from our labs suggests that the when compared to mouse samples (Mus musculus), marine mammal species demonstrated increased levels of sphingolipids and ceramides in the cell membrane. Specifically, sphingomyelin, phosphatidylcholine, ceramide, and sphingosine were elevated in the cellular membranes. While preliminary, these differences may result in changes in total cellular metabolism since these lipid constituents are known to be involved in cell signaling pathways.

Conclusion

While certainly incomplete, we have pointed out some potential advantages/disadvantages of metabolizing fatty acids in diving mammals. While it has been described that fatty acids in polar marine mammals are elevated in C16–C24 UFAs, we make an initial attempt to ascertain the beneficial adaptations or limitations of these lipids constituents. At the stoichiometric level, the metabolism of UFAs may be correlated to oxygen conservation (Suarez, 2011; Weber, 2011) while producing fewer ATP. There is evidence that indicates cellular metabolic rate is directly correlated to the PUFA composition of the membranes: birds to terrestrial mammals utilize PUFAs to conserve oxygen, possibly through lowering cardiac rate. Additionally, we speculate that ontogenetic trade-offs of fatty acids in the skeletal muscle and cellular membrane may play a vital role in the regulating changes in metabolism and establishing certain skeletal muscle adaptations (i.e., myoglobin) to diving in Weddell seals. As a current point of discussion, changes in Antarctic climate are predicted to have numerous different environmental effects; such potential shifts in the availability of certain prey species or even changes in the lipid composition (increased SFA) of numerous fish species with increasing water temperatures (Phleger et al., 1999). As we have calculated above, a slight change in fatty acid saturation could alter the diving capacity of Weddell seals. In order to clearly understand the physiology of these divers and predict how these animals will react to physiological challenges, we must understand the full suite of adaptations; from potential shifts in metabolic fuels that could affect dive times and foraging ability to understanding the molecular switches to become an efficient diver. Further research is required on the role specific lipids have on regulating homeostatic pathways. Our understanding of the role of lipids in regulating the homeostasis of the animals is in its initial stages.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors would like to thanks A. Fahlman for the invitation to publish in the Scholander Legacy. This work was supported by NSF Office of Polar Programs grants (OPP-0125475 and OPP-0440713) awarded to Shane B. Kanatous. All samples were collected under MMPA #10751788-00. We wish to thank all the personnel at Raytheon Polar services for their outstanding support as well as several colleagues for their field and lab assistance; T. Hawke, S. Noren, R. Watson, and J. Davis.

References

Billman, G. E., and Harris, W. S. (2011). Effect of dietary omega-3 fatty acids on the heart rate and the heart rate variability responses to myocardial ischemia or submaximal exercise. Am. J. Physiol. Heart Circ. Physiol. 300, H2288–H2299.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burns, J. (1996). The development of diving behavior in juvenile Weddell seals: pushing physiological limits in order to survive. Can. J. Zool. 77, 737–747.

CrossRef Full Text

Burns, J. M., Costa, D. P., Frost, K., and Harvey, J. T. (2005). Development of body oxygen stores in harbor seals: effects of age, mass, and body composition. Physiol. Biochem. Zool. 78, 1057–1068.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burns, J. M., Lestyk, K. C., Folkow, L. P., Hammill, M. O., and Blix, A. S. (2007). Size and distribution of oxygen stores in harp and hooded seals from birth to maturity. J. Comp. Physiol. B 177, 687–700.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burns, J. M., Trumble, S. J., Castellini, M. A., and Testa, J. W. (1998). The diet of Weddell seals in McMurdo Sound, Antarctica as determined from scat collections and stable isotope analysis. Polar Biol. 19, 272–282.

CrossRef Full Text

Castellini, M. A., Trumble, S. J., Mau, T. L., Yochem, P. K., Stewart, B. S., and Koski, M. A. (2009). Body and blubber measurements of Antarctic pack-ice seals: Implications for the control of body condition and blubber regulation. Physiol. Biochem. Zool. 82, 113–120.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chin, E. R., Olson, E. N., Richardson, J. A., Yang, Q., Humphries, C., Shelton, J. M., Wu, H., Zhu, W., Bassel-Duby, R., and Williams, R. S. (1998). A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type. Genes Dev. 12, 2499–2509.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Christensen, J. H., Christensen, M. S., Dyerberg, J., and Schmidt, E. B. (1999). Heart rate variability and fatty acid content of blood cell membranes: a dose-response study with n-3 fatty acids. Am. J. Clin. Nutr. 70, 331–337.

Pubmed Abstract | Pubmed Full Text

Clark, C. A., Burns, J. M., Schreer, J. F., and Hammill, M. O. (2006). Erythropoietin concentration in developing harbor seals (Phoca vitulina). Gen. Comp. Endocrinol. 147, 262–267.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Clark, C. A., Burns, J. M., Schreer, J. F., and Hammill, M. O. (2007). A longitudinal and cross-sectional analysis of total body oxygen store development in nursing harbor seals (Phoca vitulina). J. Comp. Physiol. B 177, 217–227.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Davis, R. W., Castellini, M. A., Williams, T. M., and Kooyman, G. L. (1991). Fuel homeostasis in the harbor seal during submerged swimming. J. Comp. Physiol. B 160, 627–635.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Davis, R. W., and Kanatous, S. B. (1999). Convective oxygen transport and tissue oxygen consumption in Weddell seals during aerobic dives. J. Exp. Biol. 202(Pt 9), 1091–1113.

De Miranda, M. A. Jr., Schlater, A. E., Green, T. L., and Kanatous, S. B. (2012). In the face of hypoxia: myoglobin increases in response to hypoxic conditions and lipid supplementation in cultured Weddell seal skeletal muscle cells J. Exp. Biol. 215, 806–813.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

du Dot, T. J., Rosen, D. A., Richmond, J. P., Kitaysky, A. S., Zinn, S. A., and Trites, A. W. (2009). Changes in glucocorticoids, IGF-I and thyroid hormones as indicators of nutritional stress and subsequent refeeding in Steller sea lions (Eumetopias jubatus). Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 152, 524–534.

CrossRef Full Text

Fahlman, A., Svard, C., Rosen, D. A., Jones, D. R., and Trites, A. W. (2008). Metabolic costs of foraging and the management of O2 and CO2 stores in Steller sea lions. J. Exp. Biol. 211, 3573–3580.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gales, N. J., and Burton, H. R. (1987). Ultrasonic measurement of blubber thickness of the southern elephant seal, Mirounga leonina (Linn.). Aust. J. Zool. 35, 207–217.

Gudbjarnason, S., Doell, B., Oskardottir, G., and Hallgrimsson, J. (1978). Modification of Cardiac Phospholipids and Catecholamine Stress Tolerance. Amsterdam: Elsevier.

Helge, J. W., Wu, B. J., Willer, M., Daugaard, J. R., Storlien, L. H., and Kiens, B. (2001). Training affects muscle phospholipid fatty acid composition in humans. J. Appl. Physiol. 90, 670–677.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hulbert, A. J. (2008a). Explaining longevity of different animals: is membrane fatty acid composition the missing link? Age (Dordr.) 30, 89–97.

CrossRef Full Text

Hulbert, A. J. (2008b). The links between membrane composition, metabolic rate and lifespan. Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 150, 196–203.

CrossRef Full Text

Hulbert, A. J. (2010). Metabolism and longevity: is there a role for membrane fatty acids? Integr. Comp. Biol. 50, 808–817.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hulbert, A. J., and Else, P. L. (1999). Membranes as possible pacemakers of metabolism. J. Theor. Biol. 199, 257–274.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Infante, J. P. (1987). Docosahexaenoate-containing phospholipids in sarcoplasmic reticulum and retinal photoreceptors. A proposal for a role in Ca2+-ATPase calcium transport. Mol. Cell. Biochem. 74, 111–116.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Infante, J. P., Kirwan, R. C., and Brenna, J. T. (2001). High levels of docosahexaenoic acid (22:6n-3)-containing phospholipids in high-frequency contraction muscles of hummingbirds and rattlesnakes. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 130, 291–298.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kanatous, S. B., Davis, R. W., Watson, R., Polasek, L., Williams, T. M., and Mathieu-Costello, O. (2002). Aerobic capacities in the skeletal muscles of Weddell seals: key to longer dive durations? J. Exp. Biol. 205, 3601–3608.

Pubmed Abstract | Pubmed Full Text

Kanatous, S. B., DiMichele, L. V., Cowan, D. F., and Davis, R. W. (1999). High aerobic capacities in the skeletal muscles of pinnipeds: adaptations to diving hypoxia. J. Appl. Physiol. 86, 1247–1256.

Pubmed Abstract | Pubmed Full Text

Kanatous, S. B., Elsner, R., and Mathieu-Costello, O. (2001). Muscle capillary supply in harbor seals. J. Appl. Physiol. 90, 1919–1926.

Pubmed Abstract | Pubmed Full Text

Kanatous, S. B., Hawke, T. J., Trumble, S. J., Pearson, L. E., Watson, R. R., Garry, D. J., Williams, T. M., and Davis, R. W. (2008a). The ontogeny of aerobic and diving capacity in the skeletal muscles of Weddell seals. J. Exp. Biol. 211, 2559–2565.

CrossRef Full Text

Kanatous, S. B., Pearson, L. E., and Cable, A. E. (2008b). “How do you build a marine carnivore? The potential of microarray and proteomic techniques to identify the molecular regulation of the ontogeny of skeletal muscle adaptations in Weddell seals (Leptonychotes weddellii),” in Molecules to Migration: The Pressures of Life 4th CPB Meeting in Africa: Mara 2008, eds S. Morris, and A. Vosloo (Bologna: Medimond Publishing Co.), 395–407.

Kanatous, S. B., Mammen, P. P., Rosenberg, P. B., Martin, C. M., White, M. D., Dimaio, J. M., Huang, G., Muallem, S., and Garry, D. J. (2009). Hypoxia reprograms calcium signaling and regulates myoglobin expression. Am. J. Physiol. Cell Physiol. 296, C393–C402.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kang, D., and Hamasaki, N. (2003). Mitochondrial oxidative stress and mitochondrial DNA. Clin. Chem. Lab. Med. 41, 1281–1288.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kleiber, M. (1975). The Fire of Life. Huntington, NY: Robert E. Krieger Publishing Co.

Kruger, M. C., and Horrobin, D. F. (1997). Calcium metabolism, osteoporosis and essential fatty acids: a review. Prog. Lipid Res. 36, 131–151.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Maillet, D., and Weber, J. M. (2006). Performance-enhancing role of dietary fatty acids in a long-distance migrant shorebird: the semipalmated sandpiper. J. Exp. Biol. 209, 2686–2695.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

McKenzie, D. J., Higgs, D. A., Dosanjh, B. S., Deacon, G., and Randall, D. J. (1998). Dietary fatty acid composition influences swimming performance in Atlantic salmon (Salmo salar) in seawater. Fish Physiol. Biochem. 19, 111–122.

CrossRef Full Text

Montgomery, M. K., Hulbert, A. J., and Buttemer, W. A. (2011). The long life of birds: the rat-pigeon comparison revisited. PLoS ONE 6, e24138. doi:10.1371/journal.pone.0024138

CrossRef Full Text

Nadal-Casellas, A., Amengual-Cladera, E., Proenza, A. M., Llado, I., and Gianotti, M. (2010). Long-term high-fat-diet feeding impairs mitochondrial biogenesis in liver of male and female rats. Cell. Physiol. Biochem. 26, 291–302.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Noren, S. R., Biedenbach, G., and Edwards, E. F. (2006). Ontogeny of swim performance and mechanics in bottlenose dolphins (Tursiops truncatus). J. Exp. Biol. 209, 4724–4731.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Noren, S. R., Boness, D. J., Iverson, S. J., McMillan, J., and Bowen, W. D. (2008a). Body condition at weaning affects the duration of the postweaning fast in gray seal pups (Halichoerus grypus). Physiol. Biochem. Zool. 81, 269–277.

CrossRef Full Text

Noren, S. R., Pearson, L. E., Davis, J., Trumble, S. J., and Kanatous, S. B. (2008b). Different thermoregulatory strategies in nearly weaned pup, yearling, and adult Weddell seals (Leptonychotes weddelli). Physiol. Biochem. Zool. 81, 868–879.

CrossRef Full Text

Noren, S. R., Cuccurullo, V., and Williams, T. M. (2004). The development of diving bradycardia in bottlenose dolphins (Tursiops truncatus). J. Comp. Physiol. B 174, 139–147.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Noren, S. R., Iverson, S. J., and Boness, D. J. (2005). Development of the blood and muscle oxygen stores in gray seals (Halichoerus grypus): implications for juvenile diving capacity and the necessity of a terrestrial postweaning fast. Physiol. Biochem. Zool. 78, 482–490.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pepe, S., and McLennan, P. L. (2007). (n-3) Long chain PUFA dose-dependently increase oxygen utilization efficiency and inhibit arrhythmias after saturated fat feeding in rats. J. Nutr. 137, 2377–2383.

Pubmed Abstract | Pubmed Full Text

Phleger, C. F., Nichols, P. D., Erb, E., and Williams, R. (1999). Lipids of the notothenioid fishes Trematomus spp. and Pagothenia borchgrevinki from East Antarctica. Polar Biol. 22, 241–247.

CrossRef Full Text

Piersma, T. (2011). Why marathon migrants get away with high metabolic ceilings: towards an ecology of physiological restraint. J. Exp. Biol. 214, 295–302.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ponganis, P. J., Kooyman, G. L., and Castellini, M. A. (1993). Determinants of the aerobic dive limit of Weddell seals: analysis of diving metabolic rates, postdive end tidal PO2s, and blood and muscle oxygen stores. Physiol. Zool. 66, 732–749.

Ponganis, P. J., Meir, J. U., and Williams, C. L. (2011). In pursuit of Irving and Scholander: a review of oxygen store management in seals and penguins. J. Exp. Biol. 214, 3325–3339.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ptitsyn, A., Schlater, A., and Kanatous, S. (2010). Transformation of metabolism with age and lifestyle in Antarctic seals: a case study of systems biology approach to cross-species microarray experiment. BMC Syst. Biol. 4, 133. doi:10.1186/1752-0509-4-133

CrossRef Full Text

Puertollano, M. A., Puertollano, E., Ruiz-Bravo, A., Jimenez-Valera, M., De Pablo, M. A., and De Cienfuegos, G. A. (2004). Changes in the immune functions and susceptibility to Listeria monocytogenes infection in mice fed dietary lipids. Immunol. Cell Biol. 82, 370–376.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Shiomi, K., Sato, K., and Ponganis, P. J. (2012). Point of no return in diving emperor penguins: is the timing of the decision to return limited by the number of strokes? J. Exp. Biol. 215, 135–140.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Spangenburg, E. E., and Booth, F. W. (2003). Molecular regulation of individual skeletal muscle fibre types. Acta Physiol. Scand. 178, 413–424.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Suarez, R. (2011). The biology of energy expenditure. J. Exp. Biol. 214, 163.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Trumble, S. J., Noren, S. R., Cornick, L. A., Hawke, T. J., and Kanatous, S. B. (2010). Age-related differences in skeletal muscle lipid profiles of Weddell seals: clues to developmental changes. J. Exp. Biol. 213, 1676–1684.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Valencak, T. G., Arnold, W., Tataruch, F., and Ruf, T. (2003). High content of polyunsaturated fatty acids in muscle phospholipids of a fast runner, the European brown hare (Lepus europaeus). J. Comp. Physiol. B Biochem. Syst. Environ. Physiol. 173, 695–702.

CrossRef Full Text

Weber, J. M. (2011). Metabolic fuels: regulating fluxes to select mix. J. Exp. Biol. 214, 286–294.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Weiss, L. A., Barrett-Connor, E., and von Muhlen, D. (2005). Ratio of n-6 to n-3 fatty acids and bone mineral density in older adults: the Rancho Bernardo Study. Am. J. Clin. Nutr. 81, 934–938.

Pubmed Abstract | Pubmed Full Text

Wheatley, K. E., Nichols, P. D., Hindell, M. A., Harcourt, R. G., and Bradshaw, C. J. (2008). Differential mobilization of blubber fatty acids in lactating Weddell seals: evidence for selective use. Physiol. Biochem. Zool. 81, 651–662.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Williams, C. L., Meir, J. U., and Ponganis, P. J. (2011). What triggers the aerobic dive limit? Patterns of muscle oxygen depletion during dives of emperor penguins. J. Exp. Biol. 214, 1802–1812.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Keywords: fatty acids, diving mammals, PUFA, ontogeny, lipids

Citation: Trumble SJ and Kanatous SB (2012) Fatty acid use in diving mammals: more than merely fuel. Front. Physio. 3:184. doi: 10.3389/fphys.2012.00184

Received: 09 February 2012; Accepted: 18 May 2012;
Published online: 13 June 2012.

Edited by:

Andreas Fahlman, Texas A&M Corpus Christi, USA

Reviewed by:

Tim Moerland, Kent State University, USA
Michael A. Menze, Eastern Illinois University, USA

Copyright: © 2012 Trumble and Kanatous. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.

*Correspondence: Stephen J. Trumble, Department of Biology, Baylor University, One Bear Place 97388, Waco, TX 76798, USA. e-mail: stephen_trumble@baylor.edu

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