Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Exercise endurance capacity is markedly reduced due to impaired energy homeostasis during prolonged fasting in FABP4/5 deficient mice

BMC Physiology volume 19, Article number: 1 (2019) Cite this article

Abstract

Background

Skeletal muscle prefers carbohydrate use to fatty acid (FA) use as exercise intensity increases. In contrast, skeletal muscle minimizes glucose use and relies more on FA during fasting. In mice deficient for FABP4 and FABP5 (double knockout (DKO) mice), FA utilization by red skeletal muscle and the heart is markedly reduced by the impairment of trans-endothelial FA transport, with an increase in glucose use to compensate for reduced FA uptake even during fasting. We attempted to determine whether prolonged fasting affects exercise performance in DKO mice, where constant glucose utilization occurs.

Results

A single bout of treadmill exercise was performed in the fed and fasted states. The initial speed was 10 m/min, and gradually increased by 5 m/min every 5 min up to 30 m/min until the mice stopped running. Running distance was significantly reduced by DKO genotype and prior fasting, leading to the shortest distance in fasted DKO mice. Levels of glycogen in skeletal muscle and the liver were nearly depleted in both WT and DKO mice during prolonged fasting prior to exercise. Levels of TG in skeletal muscle were not reduced by exercise in fasted DKO mice, suggesting that intramuscular TG was not utilized during exercise. Hypoglycaemia was accelerated in fasted DKO mice, and this acceleration could be due to constant glucose utilization by red skeletal muscle and the heart where FA uptake is diminished due to defective trans-endothelial FA transport. Taken together, energy supply from serum and storage in skeletal muscle were very low in fasted DKO mice, which could lead to a significant reduction in exercise performance.

Conclusions

FABP4/5 have crucial roles in nutrient homeostasis during prolonged fasting for maintaining exercise endurance capacity.

Background

Fatty acid binding proteins (FABPs) are 14–15 kDa cytosolic proteins that can reversibly bind to hydrophobic molecules such as saturated and unsaturated fatty acids (FAs) and eicosanoids with high affinity [1, 2]. It has been reported that FABPs promote the transport of lipids to specific compartments in the cells. Among FABPs, FABP4 (also referred to as A-FABP/aP2/ALBP) and FABP5 (also known as E-FABP/mal1) are abundantly expressed in adipocytes, macrophages and muscle-type capillary endothelial cells [1,2,3,4,5]. A series of studies with mice lacking both FABP4 and FABP5 (double knockout (DKO) mice) provided evidence that FABP4/5 are involved in the development of metabolic diseases, including diet-induced obesity, type 2 diabetes and insulin resistance [6,7,8]. Although it has been reported that both local and systemic inflammatory processes mediated by adipocyte and macrophage FABP4/5 can cause such metabolic diseases [1, 2, 6, 7, 9, 10], it remains obscure how the simultaneous disruption of FABP4/5 in mice exhibits remarkable effects on the amelioration of metabolic diseases.

Recent studies from our laboratory and others have reported that capillary endothelial FABP4/5 have an important role in FA transport via circulation into the heart and skeletal muscle (referred to as trans-endothelial FA transport) [3, 11,12,13]. A tracing study using 125I-BMIPP (FA tracer) and 18F-FDG (glucose tracer) revealed that DKO mice exhibit reduced FA uptake with a marked increase in glucose use in red/oxidative skeletal muscle and the heart even during fasting. Thus, trans-endothelial FA transport occurs in highly oxidative tissues with muscle type continuous capillaries, while a remarkable increase in glucose use is induced in the same tissues by a compensatory mechanism independently of insulin. These findings suggest that the ameliorating effects of FABP4/5 disruption observed in diseased models could be due to a compensatory increase in glucose use by the peripheral tissues, at least in part.

In contrast to the beneficial effects on metabolic diseases, DKO mice also exhibit an impairment of systemic metabolism when fasting is prolonged. In the fasted state in general, most tissues, except red blood cells and the brain, rely on FA use to produce energy and minimize glucose consumption [14, 15]. When fasting is prolonged, the hydrolysis of triacylglycerol (TG) in adipose tissue is accelerated, leading to an increase in plasma levels of non-esterified FA (NEFA) as the major energy substrate [14, 15]. Glycogen content in the liver becomes nearly depleted after a 24-h fast, while gluconeogenesis is accelerated to supply glucose to glucose-dependent peripheral tissues and cells [14, 15]. On the other hand, in DKO mice in the fasted state, plasma levels of NEFA are more elevated due to reduced FA uptake, which results in hepatosteatosis and hyperketonaemia [16]. In addition, the compensatory use of glucose in red skeletal muscle and the heart leads to severe hypoglycaemia, which is also at least partly caused by a reduction in gluconeogenesis [16]. Moreover, thermogenesis severely declines in fasted DKO mice when they are exposed to cold environment [17]. Major energy substrates for thermogenesis, such as glycogen in skeletal muscle, TG in brown adipose tissue and plasma glucose, become less available because they are depleted rapidly in DKO mice, which results in fatal hypothermia [17]. Thus, in DKO mice, metabolic adaptation to prolonged fasting is severely impaired due to defective FA utilization by red skeletal muscle and the heart, a compensatory use of glucose and the deranged redistribution of energy storage.

Exercise intensity influences the preference for energy substrates by skeletal muscle. When exercise intensity is low, the primary fuels are NEFA, released from adipose tissue via lipolysis, and glucose, derived from oral ingestion or the liver (gluconeogenesis or glycogenolysis) [18, 19]. As exercise intensity increases, the use of plasma glucose progressively increases, whereas the utilization of circulating NEFA declines. Simultaneously, the contribution of muscle glycogen progressively increases as well. When moderate intensity exercise continues, the contribution of the lipid oxidation in skeletal muscle is enhanced [18, 19]. Thus, exercise at a high-intensity enhances the relative contribution of carbohydrates, whereas exercise at a low to moderate intensity promotes the combustion of both carbohydrates and lipids as fuels [18, 19].

Metabolic homeostasis is impaired in DKO mice in response to fasting as described above. In this study, therefore, we studied whether exercise endurance is impaired more severely in DKO mice in the fasted state because energy provision to skeletal muscle is likely to be impaired during fasting. We found that in addition to reduced FA uptake, blood glucose levels and intramuscular energy storage were markedly decreased during fasting, which could cause a significant reduction in exercise endurance capacity in DKO mice. Our study suggests that FABP4/5 have crucial roles in nutrient homeostasis during prolonged fasting for maintaining exercise endurance capacity.

Methods

Animals and sample preparation

FABP4 and FABP5 double knockout (DKO) mice with the C57BL6j background were generated as described previously [7]. Control male wild-type (WT) mice with the C57BL6j background were purchased from Japan SLC Inc. one week before treadmill exercise training. The age (10 to 12 weeks) and body weight (22 to 27 g) of WT and DKO mice were comparable. The mice were housed and fed as described previously [20]. To reduce pain for euthanasia, the mice were briefly anaesthetized in an isoflurane-filled box to induce early unconsciousness, and then maintained using a mask type isoflurane inhalation system during blood sampling. Blood was collected from the retro-orbital plexus, and then centrifuged at 1500×g for 15 min at 4 °C to obtain the serum for measurement of biochemical parameters. After cervical dislocation, samples of the liver and skeletal muscle were dissected, snap frozen in liquid nitrogen and stored at − 80 °C until further use. All study protocols were approved by the Institutional Animal Care and Use Committee (Gunma University Graduate School of Medicine). Animal experiments were performed according to the NIH guidelines (Guide for the Care and Use of Laboratory Animals).

Treadmill exercise testing

To determine the exercise endurance capacity, treadmill exercise testing was carried out using a 2-lane motorized rodent treadmill (MK-680, Muromachi Kikai, Tokyo, Japan) [20, 21]. Mice were accustomed to the treadmill running twice, and then a single bout of running was carried out as described previously (Fig. 2b) [20, 21]. When mice stopped running more than 3 s on the electric shocker, we defined the time point as exhaustion. The total running distance for each mouse was calculated.

Measurements of glycogen and triacylglycerol

Liver and skeletal muscle were snap frozen in liquid nitrogen and then powder-pulverized. Glycogen and TG were extracted and then measured as described previously using the glycogen assay kit (BioVision, CA) and the Triglyceride E-test Wako (Wako Chemical, Osaka), respectively [3, 16].

Quantitative analysis of mRNA expression

Total RNA was isolated from liver and skeletal muscle and quantitative real time-PCR were carried out as described previously [3, 17]. The expression levels of the target genes were normalized to the level of glyceraldehyde 3-phosphate dehydrogenase (GADPH) mRNA. The Perfect Real Time Primers (ready-to-use gene-specific primers purchased from Takara Bio Inc., Shiga, Japan) were used.

Determination of myosin heavy chain isoforms in skeletal muscle

Isoform expression of myosin heavy chain (MHC) in the soleus was determined by an immunofluorescence as described previously [22]. Primary antibodies against MHC I (BA-F8) and MHC IIa (SC-71) were purchased from the Developmental Studies Hybridoma Bank (University of Iowa). Secondary antibodies (Alexa Fluor 350 IgG2b for MHC I and Alexa Fluor 555 IgG1 for MHC IIa) were purchased from Invitrogen. Wheat germ agglutinin conjugated with Alexa Fluor 488 (Invitrogen) was used to stain plasma membrane of each muscle fibre. A combination of type IIb and IIx fibres was recognized as muscle fibres negative for MHC I and MHC IIa. Muscle fibres positive or negative for each MHC isoform were counted and presented as percentage of fibre types.

Data analysis

IBM SPSS (version 24 for Windows, IBM, NY, USA) was used for statistical analysis. The results are shown as the mean ± standard deviation. A two-way analysis of variance (ANOVA) was utilized to determine the effects of feeding status (fed or fasted) on running distance between WT and DKO mice (DKO genotype). A three-way ANOVA was utilized to analyse interaction effects on gene expression and metabolites levels among exercise, DKO genotype or feeding status. P < 0.05 was considered significant. *p < 0.05, **p < 0.01, ***p < 0.001.

Results

A remarkable reduction in running distance in fasted FABP4/5 DKO mice

To test that running endurance is affected by feeding conditions in FABP4/5 DKO mice, a single bout of treadmill exercise was performed in the fed and fasted states (Fig. 1a and b). As shown in Fig. 1c, running distance was markedly reduced by fasting and DKO genotype, leading to the shortest distance in fasted DKO mice.

Fig. 1
figure 1

Running distance is significantly decreased in fasted DKO mice. (A) Eight groups prepared for this study. Ex, exercise. (B) The protocol used in this study. See the method in detail. (C) Running distance for each group. n = 6. **p < 0.01, main effect for genotype. ##p < 0.01, main effect for fasting

Full size image

Accelerated hypoglycaemia in fasted DKO mice

In search for the reasons for a reduction in endurance capacity in DKO mice during fasting, we measured biochemical parameters in the fed and fasted states with and without treadmill exercise. Serum levels of glucose were reduced by DKO genotype and fasting and increased by exercise, resulting in the lowest level in fasted DKO mice without exercise (Fig. 2a). Serum levels of NEFA were elevated by DKO genotype and fasting (Fig. 2c). Importantly, serum levels of NEFA were reduced by exercise in WT mice, while they were not altered in DKO mice (Fig. 2c, PDKO*Ex < 0.01), which is consistent with the notion that FA uptake by red skeletal muscle and the heart is reduced in DKO mice [3]. Serum levels of glycerol were elevated by exercise (Fig. 2d), suggesting that lipolysis occurred similarly in both WT and DKO mice. Levels of the β-hydroxybutyrate (BHB, ketone body) in serum were increased by DKO genotype and fasting (Fig. 2e). Interaction (Fig. 2e, PDKO*fast < 0.01 and PDKO*fast*Ex < 0.05) further suggests that compensatory utilization of the ketone body was more enhanced during exercise in fasted DKO mice compared to fasted WT mice (Fig. 2e, groups 6 and 8). Levels of lactate in serum were increased by exercise and reduced by fasting (Fig. 2f), suggesting occurrence of anaerobic glycolysis with exercise. As glucose is likely to be an important energy substrate for DKO mice even in the fasted state [3], our findings imply that marked hypoglycaemia due to fasting and FABP4/5 deficiency (Fig. 2a, groups 7 and 8) could cause detrimental effects on the exercise performance in fasted DKO mice.

Fig. 2
figure 2

Measurement of metabolites in serum. Blood was collected with or without treadmill exercise to measure serum levels of glucose (A), TG (B), NEFA (C), glycerol (D), BHB (E) and lactate (F) in the fed or fasted state. TG, triacylglycerol; NEFA, non-esterified fatty acid; BHB, β-hydroxybutyrate. n = 6. *p < 0.05, **p < 0.01, ***p < 0.001, main effect for genotype. ###p < 0.001, main effect for fasting. †††p < 0.001, main effect for exercise. Interaction is indicated with the p-value in the figure if it was statistically significant

Full size image

Accelerated depletion of energy storage in fasted DKO mice

We next examined the storage of glycogen in the liver and glycogen and TG in skeletal muscle before and after exercise. Glycogen levels in the liver were significantly decreased by fasting, leading to the depletion of glycogen in both WT and DKO mice in the fasted state prior to exercise (Fig. 3a). The marginal reduction in glycogen by exercise in the fed state was lost after a 24-h fast (Fig. 3a, Pfast*Ex < 0.05), suggesting that glycogen in the liver was unavailable for endurance exercise during prolonged fasting. Levels of glycogen in skeletal muscle were reduced by fasting and exercise (Fig. 3b). Importantly, glycogen levels seemed to be lower in fasted DKO mice after exercise compared to fasted WT mice (Fig. 3b, groups 6 and 8) despite early exhaustion (Fig. 1c), which suggests that muscle glycogen was depleted during an early phase of exercise in DKO mice. TG levels in skeletal muscle were reduced by DKO genotype, fasting and exercise (Fig. 3c). There was no reduction in TG content between pre- and post-exercise in fasted DKO mice (Fig. 3c, groups 7 and 8), suggesting no consumption of intramuscular TG during exercise in fasted DKO mice. Thus, combustion of the energy storage in the liver and skeletal muscle during exercise was markedly diminished during fasting, which is likely to worsen the energy status in DKO mice more severely.

Fig. 3
figure 3

Measurement of energy storage in liver and skeletal muscle. The liver and quadriceps femoris muscle were isolated with or without treadmill exercise in the fed or fasted state to measure glycogen and TG content. (A) Glycogen content in the liver. (B) Glycogen content in the quadriceps femoris. (C) TG content in the quadriceps femoris. TG content was normalized using protein concentration. TG, triacylglycerol. n = 6. *p < 0.05, main effect for genotype. ###p < 0.001, main effect for fasting. †††p < 0.001, main effect for exercise. Interaction is indicated with the p-value in the figure if it was statistically significant

Full size image

Expression of genes for gluconeogenesis and ketogenesis in liver was comparable between WT and DKO mice in the fasted state

Our previous report demonstrated that gluconeogenesis is markedly reduced in fasted DKO mice as shown by the pyruvate challenge test [16]. In this study, we next studied the mRNA expression of genes regulating gluconeogenesis with and without exercise in the fed and fasted states [15]. The basal expression of the glucose-6-phosphate catalytic subunit (G6pc) and phosphoenolpyruvate carboxykinase (Pck1) tended to be elevated in DKO mice (Fig. 4a, groups 1 and 3), but there were no significant main effects on their induction for DKO genotype by three-way ANOVA. Although exercise induced the expression of G6pc and Pck1 in fed WT mice, prolonged fasting blunted the effect of gene induction by exercise (Fig. 4a, Pfast*Ex < 0.01 for G6pc, Pfast*Ex < 0.05 for Pck1). These findings suggest that compensatory gluconeogenesis was not enhanced in fasted DKO mice, which could contribute to more hypoglycaemia.

Fig. 4
figure 4

Expression of genes associated with gluconeogenesis, β-oxidation and ketogenesis in liver. The liver was isolated with or without treadmill exercise in the fed or fasted state. The total RNA was extracted for quantitative real-time PCR. (A) Genes associated with gluconeogenesis. (B) Genes associated with β-oxidation. (C) Genes associated with ketogenesis. G6pc, glucose-6-phosphate catalytic subunit; Pck1, phosphoenolpyruvate carboxykinase; Hmgcs2, 3-hydroxy-3-methylglutaryl-CoA synthase 2; Ppara, peroxisome proliferator activated receptor α; Cpt1a/2, carnitine palmitoyltransferase 1a/2; Mcad, medium-chain acyl-CoA dehydrogenase; Lcad, long-chain acyl-CoA dehydrogenase. n = 6. #p < 0.05, ###p < 0.001, main effect for fasting. ††p < 0.01, main effect for exercise. Interaction is indicated with the p-value in the figure if it was statistically significant

Full size image

We next studied the mRNA expression levels of genes related to β-oxidation and ketogenesis, which were regulated by PPARA [23, 24]. The expression of Ppara and β-oxidation related genes (Cpt1a/2, Lcad and Mcad) was induced by fasting and partially affected by exercise, but not influenced by DKO genotype (Fig. 4b), suggesting that β-oxidation activity was not affected in DKO mice when compared to WT mice. The expression of Hmgcs2, a rate-limiting enzyme in ketogenesis, was increased by fasting in both WT and DKO mice (Fig. 4c). Thus, there was no enhancement of mRNA expression for gluconeogenesis or ketogenesis in the livers of fasted DKO mice during exercise, which may cause early exhaustion due to no compensatory supply of alternative energy substrates from the liver to the skeletal muscle.

Expression of genes for energy combustion in skeletal muscle was not reduced in fasted DKO mice

Next, we studied expression levels of genes associated with glucose and FA metabolism in skeletal muscle. The expression of glucose transporters Glut1 and Glut4 was induced by fasting, but not affected by DKO genotype (Fig. 5a). The induction of Glut1 by fasting was augmented in DKO mice (Fig. 5a, PDKO*fast < 0.01). Ppara, Ppard and their co-activator, PPARγ-coactivator-1 alpha (Pgc1a) are essential transcription factors controling FA combustion [19]. The expression of mRNA for Ppara and Ppard was induced by fasting and exercise but was not different between WT and DKO mice (Fig. 5b). The expression of Pgc1a was marginally elevated by DKO genotype (Fig. 5b). Consist with these data, the expression of target genes of the PPAR/PGC-1 complex was not significantly influenced by DKO genotype, except Cd36 (Fig. 5c). Thus, there is only a minor difference in terms of the expression of genes associated with glucose and FA metabolism in skeletal muscle, which is unlikely to compensate for reduced energy supply during exercise in fasted DKO mice.

Fig. 5
figure 5

Expression of genes associated with energy metabolism in skeletal muscle. The quadriceps femoris muscle was isolated with or without treadmill exercise in the fed or fasted state. The total RNA was extracted for quantitative real-time PCR. (A) Genes associated with glucose uptake. (B) Genes of central regulators for FA metabolism. (C) Genes associated with β-oxidation and FA uptake. Glut1/4, glucose transporter 1/4; Ppara, peroxisome proliferator activated receptor α; Ppard, Ppar δ, Pgc1a, PPARG coactivator 1α. n = 6. *p < 0.05, main effect for genotype. #p < 0.05, ##p < 0.01, ###p < 0.001, main effect for fasting, †p < 0.05, ††p < 0.01, main effect for exercise. Interaction is indicated with the p-value in the figure if it was statistically significant

Full size image

Composition of fibre types in oxidative skeletal muscle was comparable

Oxidative red muscle fibres, which mainly utilize FA, are fatigue-resistant whereas glycolytic white fibres, which rely on more glucose, are susceptible to fatigue [19, 25]. As red/oxidative muscle consumes more glucose in DKO mice, we questioned whether a shift of energy substrates from FA to glucose affects muscle fibre types, which might, in turn, cause an early exhaustion upon exercise during fasting. To determine muscle fibre types in oxidative muscle (i.e., the soleus), immunofluorescence was performed to detect myosin heavy chain (MHC) isoforms (type I, oxidative fibre; type IIb and IIx, glycolytic fibres; type IIb, characteristics between oxidative and glycolytic fibres) [22]. As shown in Fig. 6, there was no significant difference regarding the composition of MHC isoforms. Thus, our data suggest that a reduction in exercise endurance is not caused by the phenotypic change of muscle fibre types.

Fig. 6
figure 6

Expression of MHC isoforms in skeletal muscle. The soleus muscle was isolated in WT and DKO mice to estimate the expression of MHC isoforms by immunofluorescence. MHC I and MHC IIa were stained with blue and red, respectively. Muscle fibres negative for MHC I and MHC IIa were represented as a combination of type IIb and IIx fibres. The bar graph shows the percentage of each MHC isoform. MHC, myosin heavy chain. n = 6. Scale bar, 100 μm

Full size image

Discussion

We demonstrated that FABP4/5 have a critical role in exercise endurance in the fasted state. Energy storage, such as glycogen in the liver and glycogen and TG in skeletal muscle, were almost depleted in fasted DKO mice. Accelerated utilization of glucose in oxidative muscle and the heart is maintained even during fasting and gluconeogenesis is diminished [3], which could result in accelerated hypoglycaemia. Further, FA uptake is decreased in oxidative muscle due to defective trans-endothelial FA transport via capillary endothelial FABP4/5 [3, 16]. As a result, energy supply from serum and energy storage in skeletal muscle are very low in fasted DKO mice prior to exercise, which could bring about a significant reduction in exercise performance. We conclude that deranged uptake and redistribution of energy substrates during prolonged fasting provoke maladaptive energy homeostasis, leading to a significant reduction in exercise endurance capacity.

It is noteworthy that exercise performance was not reduced much in DKO mice compared to WT mice in the fed state (Fig. 1c) when glycogen and TG storage was fulfilled (Fig. 3b and c). We recently reported similar findings in CD36 knockout (KO) mice [20]. Like FABP4/5 DKO mice, CD36KO mice also display a reduction in FA transport and oxidation with a compensatory use of glucose [26, 27]. In CD36KO mice, endurance capacity is severely reduced in the fasted state, while the reduction is modest in the fed state [20]. These findings further support the notion that intact FA utilization by peripheral tissues plays an important role in nutrient homeostasis in the fasted state to maintain the exercise endurance capacity. In contrast to our observation, however, previous studies showed a reduction in exercise endurance capacity in CD36KO mice even during fasting [28,29,30]. However, between our studies and previous reports with CD36KO mice, there is a major difference regarding the exercise protocols. The treadmill speed used in previous studies was 17 m/min or less (mild to moderate intensity) [28,29,30]. In our studies, the exercise speed was increased up to 30 m/min in a single bout (high intensity). High-intensity exercise induces maximum reliance on glycogen in skeletal muscle, while mild to moderate intensity exercise leads to modest reliance on intramuscular glycogen and TG, as well as circulating NEFA [31]. In addition to energy reliance, mild to moderate intensity exercise results in a longer exercise time (hours), which could, in turn, augment the relative contribution of FABP4/5/CD36-mediated FA uptake from the circulation. Thus, exercise intensity, as well as duration, affects the preference for main energy substrates for endurance, which can cause differences in the endurance capacity between WT mice and mice with defective FA utilization. In the fed state, endurance capacity for high intensity exercise is more affected by glycogen content in skeletal muscle, whereas the capacity for mild to moderate intensity exercise is more influenced by the FA uptake ability.

In addition to an enhanced reduction in endurance capacity, we reported that DKO mice exhibit lethal hypothermia in response to cold exposure in the fasted state [17]. Accelerated hypothermia during fasting is mainly caused by a marked reduction in TG storage in brown adipose tissue, glycogen in skeletal muscle and blood glucose. Importantly, rapid hypothermia does not occur in the fed state, when energy storage in brown adipose tissue and skeletal muscle is filled. Thus, an inappropriate redistribution of energy substrates occurs in DKO mice only in the fasted state, which leads to the depletion of tissue energy storage for thermogenesis and exercise. Similar responses during fasting were also observed in CD36KO mice, another model with defective FA utilization [20, 32], suggesting that such physiological disadvantages during fasting seem to be a common feature in animals with defective FA utilization. These findings further provide an important notion that in general, appropriate FA utilization by peripheral tissues is essential to adapt to severe natural environments such as famine and coldness, and to chase animals or escape from natural enemies during fasting.

There is accumulating evidence that the gut microbiota plays a role in the host metabolic status as a mediator of dietary intake [33, 34]. Germ-free mice have reduced adiposity, improved tolerance to glucose and insulin and are protected from diet-induced obesity when fed a Western diet [33, 34]. It has also been suggested that an altered composition of the microbiota is associated with increased host adiposity via a number of different mechanisms [33, 34]. In addition, the mouse microbiota is known to be heavily affected by their environment. In this study, control WT mice were purchased from an outside vendor one week before treadmill exercise training, while DKO mice were born and grown in our animal facility. Thus, the difference of housing conditions between WT and DKO mice might affect the results of metabolic data to a certain degree, which needs careful interpretation.

In our previous studies, we estimated cardiac function in DKO mice in pressure overload-induced and lipopolysaccharide-induced cardiomyopathy models [35, 36]. Cardiac dysfunction was more obvious in DKO mice compared to WT mice in both models, presumably due to energy depletion. Interestingly, however, induction levels of mRNA for natriuretic peptide b (Nppb), a marker of cardiac stress, were comparable in WT and DKO mice, suggesting that cardiac dysfunction occurs by energy depletion with no change of Nppb expression levels (unpublished observation). In this study, we also found comparable induction of Nppb in WT and DKO mice after exercise in the fasted state. Based on our previous observation, the result does not necessarily mean that cardiac function is similar between WT and DKO mice. Thus, the possibility that a reduction in exercise endurance capacity in DKO is caused by cardiac dysfunction remains unsolved.

Conclusions

FA uptake by peripheral tissues via capillary endothelial FABP4/5 has crucial roles in nutrient homeostasis for maintaining exercise endurance capacity during prolonged fasting.

Abbreviations

ATP:

Adenosine triphosphate

BHB:

β-hydroxybutyrate

Cpt1b/2:

Carnitine palmitoyltransferase 1b/2

DKO:

Double knockout

FA:

Fatty acid

FABP:

Fatty acid binding protein

G6pc:

Glucose-6-phosphate catalytic subunit

Gapdh:

Glyceraldehyde 3-phosphate dehydrogenase

Glut1/4:

Glucose transporter 1/4

Hmgcs2:

3-hydroxy-3-methylglutaryl-CoA synthase 2

Lcad:

Long-chain acyl-CoA dehydrogenase

Mcad:

Medium-chain acyl-CoA dehydrogenase

MHC:

Myosin heavy chain

NEFA:

Non-esterified fatty acid

Pck1:

Phosphoenolpyruvate carboxykinase

Pgc1a:

Peroxisome proliferator activated receptor γ coactivator 1 alpha

Ppara:

Peroxisome proliferator activated receptor α

Ppard:

Peroxisome proliferator activated receptor δ

TG:

Triacylglycerol

WT:

Wild type

References

  1. Hotamisligil GS, Bernlohr DA. Metabolic functions of FABPs--mechanisms and therapeutic implications. Nat Rev Endocrinol. 2015;11:592–605.

    Article  CAS  Google Scholar 

  2. Furuhashi M, Hotamisligil GS. Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets. Nat Rev Drug Discov. 2008;7:489–503.

    Article  CAS  Google Scholar 

  3. Iso T, Maeda K, Hanaoka H, Suga T, Goto K, et al. Capillary endothelial fatty acid binding proteins 4 and 5 play a critical role in fatty acid uptake in heart and skeletal muscle. Arterioscler Thromb Vasc Biol. 2013;33:2549–57.

    Article  CAS  Google Scholar 

  4. Elmasri H, Karaaslan C, Teper Y, Ghelfi E, Weng M, et al. Fatty acid binding protein 4 is a target of VEGF and a regulator of cell proliferation in endothelial cells. FASEB J. 2009;23:3865–73.

    Article  CAS  Google Scholar 

  5. Masouye I, Hagens G, Van Kuppevelt TH, Madsen P, Saurat JH, et al. Endothelial cells of the human microvasculature express epidermal fatty acid-binding protein. Circ Res. 1997;81:297–303.

    Article  CAS  Google Scholar 

  6. Furuhashi M, Fucho R, Gorgun CZ, Tuncman G, Cao H, et al. Adipocyte/macrophage fatty acid-binding proteins contribute to metabolic deterioration through actions in both macrophages and adipocytes in mice. J Clin Invest. 2008;118:2640–50.

    CAS  PubMed  PubMed Central  Google Scholar 

  7. Maeda K, Cao H, Kono K, Gorgun CZ, Furuhashi M, et al. Adipocyte/MACROPHAGE fatty acid binding proteins control integrated metabolic responses in obesity and diabetes. Cell Metab. 2005;1:107–19.

    Article  CAS  Google Scholar 

  8. Boord JB, Maeda K, Makowski L, Babaev VR, Fazio S, et al. Combined adipocyte-macrophage fatty acid-binding protein deficiency improves metabolism, atherosclerosis, and survival in apolipoprotein E-deficient mice. Circulation. 2004;110:1492–8.

    Article  CAS  Google Scholar 

  9. Cao H, Sekiya M, Ertunc ME, Burak MF, Mayers JR, et al. Adipocyte lipid chaperone AP2 is a secreted adipokine regulating hepatic glucose production. Cell Metab. 2013;17:768–78.

    Article  Google Scholar 

  10. Cao H, Gerhold K, Mayers JR, Wiest MM, Watkins SM, et al. Identification of a lipokine, a lipid hormone linking adipose tissue to systemic metabolism. Cell. 2008;134:933–44.

    Article  CAS  Google Scholar 

  11. Coppiello G, Collantes M, Sirerol-Piquer MS, Vandenwijngaert S, Schoors S, et al. Meox2/Tcf15 heterodimers program the heart capillary endothelium for cardiac fatty acid uptake. Circulation. 2015;131:815–26.

    Article  CAS  Google Scholar 

  12. Goto K, Iso T, Hanaoka H, Yamaguchi A, Suga T, et al. Peroxisome proliferator-activated receptor-gamma in capillary endothelia promotes fatty acid uptake by heart during long-term fasting. J Am Heart Assoc. 2013;2:e004861.

    Article  Google Scholar 

  13. Kanda T, Brown JD, Orasanu G, Vogel S, Gonzalez FJ, et al. PPARgamma in the endothelium regulates metabolic responses to high-fat diet in mice. J Clin Invest. 2009;119:110–24.

    CAS  PubMed  Google Scholar 

  14. Marray RK, editor. Harper's illustrated biochemistry. 28th ed. New York: McGraw-Hill Companies, Inc.; 2009.

    Google Scholar 

  15. Salway JG, editor. Metabolism at a glance. 3rd ed. Oxford: Blackwell Publishing; 2004.

    Google Scholar 

  16. Syamsunarno MR, Iso T, Hanaoka H, Yamaguchi A, Obokata M, et al. A critical role of fatty acid binding protein 4 and 5 (FABP4/5) in the systemic response to fasting. PLoS One. 2013;8:e79386.

    Article  Google Scholar 

  17. Syamsunarno MR, Iso T, Yamaguchi A, Hanaoka H, Putri M, et al. Fatty acid binding protein 4 and 5 play a crucial role in thermogenesis under the conditions of fasting and cold stress. PLoS One. 2014;9:e90825.

    Article  Google Scholar 

  18. Yoshida Y, Jain SS, McFarlan JT, Snook LA, Chabowski A, et al. Exercise- and training-induced upregulation of skeletal muscle fatty acid oxidation are not solely dependent on mitochondrial machinery and biogenesis. J Physiol. 2013;591:4415–26.

    Article  CAS  Google Scholar 

  19. Egan B, Zierath JR. Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metab. 2013;17:162–84.

    Article  CAS  Google Scholar 

  20. Iso T, Haruyama H, Sunaga H, Matsui H, Matsui M, et al. CD36 is indispensable for nutrient homeostasis and endurance exercise capacity during prolonged fasting. Physiol Rep. 2018;6:e13884.

    Article  Google Scholar 

  21. Haramizu S, Nagasawa A, Ota N, Hase T, Tokimitsu I, et al. Different contribution of muscle and liver lipid metabolism to endurance capacity and obesity susceptibility of mice. J Appl Physiol. 2009;106:871–9.

    Article  CAS  Google Scholar 

  22. Bloemberg D, Quadrilatero J. Rapid determination of myosin heavy chain expression in rat, mouse, and human skeletal muscle using multicolor immunofluorescence analysis. PLoS One. 2012;7:e35273.

    Article  CAS  Google Scholar 

  23. Puchalska P, Crawford PA. Multi-dimensional roles of ketone bodies in fuel metabolism, signaling, and therapeutics. Cell Metab. 2017;25:262–84.

    Article  CAS  Google Scholar 

  24. Grabacka M, Pierzchalska M, Dean M, Reiss K. Regulation of ketone body metabolism and the role of PPARalpha. Int J Mol Sci. 2016;17:e2093.

  25. Wang YX, Zhang CL, Yu RT, Cho HK, Nelson MC, et al. Regulation of muscle fiber type and running endurance by PPARdelta. PLoS Biol. 2004;2:e294.

    Article  Google Scholar 

  26. Hajri T, Han XX, Bonen A, Abumrad NA. Defective fatty acid uptake modulates insulin responsiveness and metabolic responses to diet in CD36-null mice. J Clin Invest. 2002;109:1381–9.

    Article  CAS  Google Scholar 

  27. Coburn CT, Knapp FF Jr, Febbraio M, Beets AL, Silverstein RL, et al. Defective uptake and utilization of long chain fatty acids in muscle and adipose tissues of CD36 knockout mice. J Biol Chem. 2000;275:32523–9.

    Article  CAS  Google Scholar 

  28. Manio MCC, Matsumura S, Masuda D, Inoue K. CD36 is essential for endurance improvement, changes in whole-body metabolism, and efficient PPAR-related transcriptional responses in the muscle with exercise training. Physiol Rep. 2017;5:e13282.

  29. Fujitani M, Matsumura S, Masuda D, Yamashita S, Fushiki T, et al. CD36, but not GPR120, is required for efficient fatty acid utilization during endurance exercise. Biosci Biotechnol Biochem. 2014;78:1871–8.

    Article  CAS  Google Scholar 

  30. McFarlan JT, Yoshida Y, Jain SS, Han XX, Snook LA, et al. In vivo, fatty acid translocase (CD36) critically regulates skeletal muscle fuel selection, exercise performance, and training-induced adaptation of fatty acid oxidation. J Biol Chem. 2012;287:23502–16.

    Article  CAS  Google Scholar 

  31. Romijn JA, Coyle EF, Sidossis LS, Gastaldelli A, Horowitz JF, et al. Regulation of endogenous fat and carbohydrate metabolism in relation to exercise intensity and duration. Am J Phys. 1993;265:E380–91.

    CAS  Google Scholar 

  32. Putri M, Syamsunarno MR, Iso T, Yamaguchi A, Hanaoka H, et al. CD36 is indispensable for thermogenesis under conditions of fasting and cold stress. Biochem Biophys Res Commun. 2015;457:520–5.

    Article  CAS  Google Scholar 

  33. Sonnenburg JL, Backhed F. Diet-microbiota interactions as moderators of human metabolism. Nature. 2016;535:56–64.

    Article  CAS  Google Scholar 

  34. Nehra V, Allen JM, Mailing LJ, Kashyap PC, Woods JA. Gut microbiota: modulation of host physiology in obesity. Physiology (Bethesda). 2016;31:327–35.

    CAS  Google Scholar 

  35. Umbarawan Y, Syamsunarno M, Koitabashi N, Yamaguchi A, Hanaoka H, et al. Glucose is preferentially utilized for biomass synthesis in pressure-overloaded hearts: evidence from fatty acid-binding protein-4 and -5 knockout mice. Cardiovasc Res. 2018;114:1132–44.

    Article  Google Scholar 

  36. Umbarawan Y, Syamsunarno M, Obinata H, Yamaguchi A, Sunaga H, et al. Robust suppression of cardiac energy catabolism with marked accumulation of energy substrates during lipopolysaccharide-induced cardiac dysfunction in mice. Metabolism. 2017;77:47–57.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank Takako Kobayashi and Keiko Matsukura for excellent technical help. We thank Drs. Hiroshi Yorifuji and Hitoshi Ueno for technical help with the treadmill exercise.

Funding

This work including collection and analysis of data was supported in part by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (no. 16H05294 to MK and no. 17 K09568 to TI), a grant from the Gunma University Initiative for Advanced Research (no. 140908272400 to MK), and a grant from the Japan Agency for Medical Research and Development (no. 10030–14120 to MK).

Availability of data and materials

The datasets used and/or analysed in the current study are available from the corresponding author upon reasonable request.

Author information

Authors and Affiliations

  1. Department of Cardiovascular Medicine, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan

    Tatsuya Iso, Hiroaki Sunaga, Miki Matsui, Yogi Umbarawan, Mas Rizky A. A. Syamsunarno & Masahiko Kurabayashi

  2. Department of Laboratory Sciences, Gunma University Graduate School of Health Sciences, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan

    Hikari Haruyama, Hiroki Matsui, Rina Tanaka & Tomoyuki Yokoyama

  3. Department of Internal Medicine, Faculty of Medicine Universitas Indonesia, Jl. Salemba Raya no. 6, Jakarta, 10430, Indonesia

    Yogi Umbarawan

  4. Department of Biochemistry and Molecular Biology, Universitas Padjadjaran, Jl. Raya Bandung Sumedang KM 21, Jatinangor, West Java, 45363, Indonesia

    Mas Rizky A. A. Syamsunarno

Authors
  1. Tatsuya Iso
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Hikari Haruyama
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Hiroaki Sunaga
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Miki Matsui
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Hiroki Matsui
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Rina Tanaka
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Yogi Umbarawan
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Mas Rizky A. A. Syamsunarno
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Tomoyuki Yokoyama
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Masahiko Kurabayashi
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

TI designed this study. HH, HS, MM, HM, YU, MRAAS, TY and TI collected physiological and biochemical data via treadmill exercise. HH and RT performed the immunofluorescence. HH and TI analysed all the data. TI and MK contributed to the manuscript writing. The final version of the manuscript was approved by all authors.

Corresponding author

Correspondence to Tatsuya Iso.

Ethics declarations

Ethics approval and consent to participate

All study protocols were approved by the Institutional Animal Care and Use Committee (Gunma University Graduate School of Medicine) and were performed in accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Iso, T., Haruyama, H., Sunaga, H. et al. Exercise endurance capacity is markedly reduced due to impaired energy homeostasis during prolonged fasting in FABP4/5 deficient mice. BMC Physiol 19, 1 (2019). https://doi.org/10.1186/s12899-019-0038-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12899-019-0038-6

Keywords

BMC Physiology

ISSN: 1472-6793

Contact us