Corresponding author: Ho Youl Kang. Department of Physical Education, Kyungpook National University, 1370 Sankyuk-dong, Buk-gu, Daegu 702-701, Korea. INTRODUCTION
Due to the westernization of diet and the lack of exercise, obesity is rapidly spreading throughout the country in Korea. Also, the World Health Organization (WHO) has said that if the estimated number of obese adults in the world is in the mid 400 millions (body mass index ≥ 30), then by 2015, the number of obese individuals is expected to reach 700 millions [1].
The consumptions of high fat diet are resulting in increased general insulin levels and insulin resistance in muscles and in the body overall. It has been reported that increased insulin level due to a high fat diet causes hyperglycemia and, if left untreated, will increase the likelihood of developing type 2 diabetes mellitus [2-5]. Also, the intake of a high fat diet in obese type 2 diabetic patients causes muscular fat to oxidize less, increasing the accumulation of fat in adipocytes and muscle tissues. Accumulation of lipids within the skeletal muscles increases long-chain fatty acyl CoAs (LCACoAs), diaglycerol (DAG), ceramide among other mid-products. This occurs simultaneously with insulin signal transduction, which causes a decrease in the frequency of glucose transporter 4 (GLUT-4) translocation. As a result, it is reported that glucose uptake in the muscles is decreased, and muscle's insulin resistance is increased [1,6]. Among the mid-products, ceramide affects the cellular proliferation, cellular division, and inflammatory response [7], and it also takes a noticeable effect on glucose uptake and insulin signaling [8]. Previous studies have reported that ceramide is increased in insulin resistant muscles [8-11], which decreases the phosphorylation of insulin receptor substrate-1 among other insulin signaling structures that affect GLUT-4's translocation and limits the activity of phosphatidyl inositol-3 kinase. It also brings about insulin resistance by limiting phosphorylation of protein kinase B (Akt/PKB) [12-14]. Insulin resistance is observed as a result of a surplus of lipids which is thought to be caused by an accumulation of ceramide in the liver and muscle tissue. Reduction of the ceramide in the skeletal muscle tissue could improve the insulin resistance.
Previous data on the improvement of insulin resistance have shown relationship between regular exercise and reduced insulin resistance [15-18]. Ivy [18] reported insulin stimulated glucose transport during intense training. Dobrzyn and Gorski [19] reported that sustained light cardiovascular exercise decreases muscular ceramide and neutral Mg++ dependent sphingomyelinase (nSMase) concentrations. Additionally, it is reported that intensity exercise decrease the concentration of sphingosine and sphinganine and that the effectiveness of the metabolism of ceramide increases. Along with this exercise decreases muscular insulin resistance. Studies regarding muscular glucose uptake have been performed and continue to advance. However, studies about exercise, ceramide, muscular triglyceride, and glucose transport rates do not yet exist. Thus, in this experiment, we will explore whether a high fat diet paired with endurance exercises will have an effect on the insulin resistance and ceramide content in skeletal muscles.
METHODS
Experimental animals
In this experiment, 32 male Sprague-Dawley (SD) rats were were divided into four groups and were raised individually in separate (20.7 × 35 × 17 cm) cages. The rats were kept under a constant temperature of 21℃, and exposure to light was regulated in 12 hour intervals 12 hours (7:00-19:00) of darkness, and 12 hours of light (19:00-7:00). After a one-week environmental adaptation period, subjects were randomly placed into control group (CON), high fat diet group (HF), exercise group (Ex), and high fat diet/exercise group (HF/Ex).
Measurements and methods
Experimental procedure
The high fat diet group was provided with 40% beef tallow high fat feed (#101556 AIN-76A; Dyets Inc., Bethlehem, PA, USA), and the remaining groups were given regular feed (#100000 AIN-76A; Dyets Inc.). Food and water were provided ad libitum, and endurance training was implemented and regulated by a motorized treadmill (Jeonkook Machinery Co., Seoul, Korea) set at an 8% gradient. Rats exercised 5 times per week for 4 weeks. The treadmill speed and duration were gradually increased, and exercise implementation at 4 weeks was 24 m/min for 2 hours. The final bout of exercise was not performed in order to exclude the effects of exercise 24 hours prior to tissue sampling. After the 4 week study, the rats were forced to fast for 12 hours, after which they were injected with 6.5 mg of anesthetic (pentobarbital sodium) per 100 g of body weight, then muscle was removed and frozen with liquid nitrogen, and blood samples were collected from abdominal aorta, and plasma was separated via centrifuge and stored at -70℃. The soleus muscle was used to measure the glucose transport rate immediately after sampling.
Plasma lipid concentration
Total cholesterol (TC) and triglycerides (TG) were determined by an enzymatic method (Elitech, See, France). Free fatty acid (FFA) was measured using Noma's method [20].
Plasma glucose and insulin measurement
Plasma glucose levels were measured using a YSI 1500 blood and lactate analyzer (Yellow Spring Instrument Co., Yellow Springs, OH, USA). Insulin was measured with radioimmunoassay method using a diagnostic kit (Lincoplex Research Inc., St. Louis, MO, USA).
Skeletal muscle and liver TG
The plantaris muscle was homogenized in buffer solution (50 mM potassium floride + 1 mM EDTA, pH 7.4) with 1 : 20 dilution, and the liver was homogenized with buffer solution (50 mM potassium phosphate + 1 mM EDTA, pH 7.4) as 1 : 10 dilution. The homogenized sample was mixed with SDS (100 mM), ethanol, n-heptane in order, and then centrifuged at 1,000 × g for 10 minutes. The supernatant was transferred to a tube, dried for 12 hours, and then the remaining liquid was completely evaporated using nitrogen gas. TG in the tube was dissolved with isopropanol, and then the concentration of TG was measured using diagnostic reagent (Elitech).
Skeletal muscle ceramide content
Ceramide was measured using adenosine 5-[γ-32P] triphosphate [21]. The plantaris muscle was homogenized using Tris potassium chloride buffer (0.25 M sucrose, 25 mM KCl, 50 mM Tris, 0.5 mM EDTA, pH 7.4) with 1 : 10 dilution, and then lipid was extracted using the Burton method [22]. The experimental standard for ceramide used was: (brain; Avanti polar lipid Inc., Albastar, AL, USA). Extracted fat and ceramide standard was dissolved in 1,2-dioleoyl-sn-glycero-3-[phosphor-rac-(1-glycerol)] (DOPG) solution, was evaporated under nitrogen gas, and then re-dissolved using n-Octyl-β-D-glucopyranoside (β-OG) solution, vortex mixed to form micelles, and then it was incubated in 4℃ for 12 hours. DAG kinase reaction mixture (100 mM imidazole; pH 6.6, 100 mM LiCl, 25 mM MgCl2, 2 mM EGTA, 4 mM dithiothreitol, DAG kinase) and initiation mixture (10 mM imidazole; pH 6.6, 1 mM EDTA, 5 mM [32P]-γ-ATP) were added to a culture medium in order to make a DAG kinase reaction. It was then cultured at 26℃ for 30 minutes. Afterwards, lipid was extracted and then the remainder was evaporated using nitrogen gas. The lipid extract was eluted by adding chloroform/methanol (4 : 1, v/v) 40 µL. After dividing the mixture into 60 silica gel plates, the depths of each TLC chamber was set between 0.5-1 cm and then a solution composed of chloroform, acetone, methanol, acetic acid, and water (10 : 4 : 3 : 2 : 1, v/v) was added and then filtered to remove any bubbles, and following that, silica gel plates were inserted. After sample loading was completed, the plates were taken out and air dried. The plates were then exposed to X-ray film at -20℃ for 12 hours. Then, ceramide 1-[32P] phosphate's activity was measured for one minute per plate using a liquid scintillation counter (Wallac 1409 DSA; PerkinElmer Inc., Waltham, MA, USA).
Skeletal muscle GLUT-4
After separating gastronemius muscle into red gastronemius (RG), and white gastronemius (WG), they were mixed with a cold 1 : 20 HEPES buffer (20 mM N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid, 1 mM EDTA, and 250 mM sucrose, pH 7.4), and then homogenized using a polytron homogenizer (Kinematica, Littau, Switzerland). Homogenized muscle tissue was diluted using 1 : 2 2x Laemmli sample buffer (S3401; Sigma-Aldrich, St. Louis, MO, USA), left out at room temperature for 20 minutes, and then 75 µg of protein containing sample was loaded into 10% SDS-polyacrylamide gel electrophoresis (PAGE), electrophoresis was initiated (100-120 V, 60-90 minutes). Standardization of GLUT-4 in each gel was verified by GLUT-4 content in 50 µg of rat cardiac muscle [23]. After electrophoresis was completed, the gel was divided and then using semi-dry (BioRad, Hercules, CA, USA), the gel was transferred to a PVDF membrane (BioRad). The transferred membrane was blocked in 5% non-fat skim milk for 60 minutes, and then incubated with GLUT-4 antiserum (Santa Cruz Biotechology, Santa Cruz, CA, USA) diluted to a 1 : 10,000 mixture (T-TBS/5% non-fat skin milk), and was shaken and incubated for 90 minutes. After washing, secondary antibodies (ZYMED Laboratories, South San Francisco, CA, USA) were diluted into a 1 : 5,000 ratio (T-TBS/1% non-fat skin milk) and incubated for 60 minutes. The GLUT-4 protein was visualized by Hyperfilm (Eastman Kodak, Rochester, NY, USA) using the Western blot luminal reagent (Santa Cruz Biotechology).
Rate of glucose transport in skeletal muscle
Glucose transport rate was measured using Methyl [3H]-D-glucose and D-[1-14C] mannitol [24]. For the sake of measurement, thin portions (20-30 mg) of the left soleus muscle were extracted for use, and the removal of the muscular glucose, it was cleaned a single time with 18 mM mannitol and 0.1% BSA, + 2 mM pyruvate containing KHB for 10 minutes. After the initial cleaning, it was again incubated in 16 mM mannitol and 0.1% BSA, + 4 mM glucose + (with/without) Insulin (1,000 µIU/mL) containing [25,26] KHB for 30 minutes, cultured, and then cleaned for another 10 minutes. Afterwards, it was once again incubated at 30℃ in 4 mM [3-3H] MG (2.2 µCi/mL) and 16 mM [14C] mannitol (0.2 µCi/mL) containing 1.5 mL KHB. After culturing, the soleus muscle was fixed with liquid nitrogen and was immediately weighed. The weighed muscle was placed in 1 N NaOH and then put in a 50-60℃ water bath and shaken for 60 minutes. Afterwards, it was separated via centrifuge at 1,600 rpms for 4 minutes. The supernatant was removed and then after adding Optiphase Hisafe 2, it was measured with a liquid scintillation counter (Wallac 1220 Quantulus; PerkinElmer Inc.) for 10 minutes.
Statistical analysis
The mean and standard error (Mean ± SE) of each measurement was calculated, and statistical analysis was done using the statistics program, SPSS version 17.0 (SPSS Inc., Chicago, IL, USA). One-way ANOVA was used to see the change between groups after handling. Least significant difference (LSD) was used for post hoc analysis. The statistical significance was defined as P < 0.05.
RESULTS
Weight
After 4 weeks, the weight of the Ex group (293.9 ± 19.0 g) was compared with the other three groups (313.1 ± 4.1 g, 311.6 ± 4.6 g, 276.9 ± 3.3 g, respectively, P = 0.000) with notable differences between them. The weight of HF/Ex group (276.9 ± 3.3 g) was significantly lower than the other three groups (313.1 ± 4.1 g, 293.9 ± 19.0 g, 311.6 ± 4.6 g, respectively, P = 0.000) (Fig. 1).
Blood plasma lipid
Four weeks after the experimental period, the measured FFA concentrations of the CON and HF groups were significantly higher than in the Ex group (P = 0.032). The TC concentration in the HF group was significantly higher than the other three groups (P = 0.000). The concentration of TG in the HF and HF/Ex groups was significantly higher than the concentration in the CON and Ex groups, and concentration in the HF/Ex group was higher than the concentration in the HF group (P < 0.001) (Table 1).
Plasma glucose and insulin
Plasma glucose concentrations of groups Ex and HF/Ex 297.1 ± 14.9 mg/dL, 269.8 ± 9.1 mg/dL, respectively) were lower than the HF group (361.2 ± 19.0 mg/dL), and the concentration in the HF/Ex group was significantly lower than the concentration in the CON group (321.9 ± 1.3 mg/dL) (P = 0.002) (Fig. 2). The insulin concentration in the HF group (57.1 ± 6.4 µIU/mL) was significantly high compared to the other three groups (32.4 ± 5.5 µIU/mL, 28.6 ± 7.0 µIU/mL, 31.2 ± 8.0 µIU/mL, respectively, P = 0.021) (Fig. 3).
TG in muscle and the liver
The TG content in the plantaris muscle of the Ex group (5.7 ± 0.8 µmol/gww) was significantly lower than the HF/Ex group (10.4 ± 1.2 µmol/gww), and was significantly higher in the HF group (12.2 ± 1.7 µmol/gww) than in the CON and Ex groups (7.2 ± 1.4 µmol/gww, 5.7 ± 0.8 µmol/gww, respectively, P = 0.005). The TG content in the liver of the Ex group (18.7 ± 0.3 µmol/gww) was significantly lower than in the HF/Ex group (22.4 ± 0.7 µmol/gww), and was significantly higher in the HF group (34.9 ± 1.9 µmol/gww) than in the other three groups (P = 0.000) (Fig. 4).
Skeletal muscle ceramide
Ceramide contents in the plantaris muscle in the Ex and HF/Ex (74.3 ± 4.0 pmol/mg, 67.1 ± 4.5 pmol/mg, respectively) groups were significantly lower than in the HF group (96.0 ± 9.5 pmol/mg, P = 0.031, Fig. 5).
Skeletal muscle GLUT-4
The GLUT-4 in the RG muscle in the Ex and HF/Ex groups (81.6 ± 6.8%, 74.8 ± 6.9%, respectively) was significantly higher than in the CON and HF groups (56.4 ± 5.3%, 54.1 ± 5.9%, respectively, P = 0.009). In the WG muscle, GLUT-4 in the Ex and HF/Ex (30.8 ± 2.8%, 31.2 ± 2.9%, respectively) groups were significantly higher than in the CON and HF groups (18.1 ± 2.5%, 20.2 ± 2.8%, respectively, P = 0.003, Fig. 6).
Glucose transport rate in skeletal muscle
The glucose transport rate in the soleus muscle in insulin-free conditions was very similar in all four groups. However, in submaximal conditions, the glucose transport rates in the Ex and HF/Ex (3.3 ± 0.4 µmol/mL/hr, 3.3 ± 0.4 µmol/mL/hr, respectively) groups are much higher than in the CON group (2.2 ± 0.2 µmol/mL/hr) (P = 0.043) (Fig. 7).
DISCUSSION
In the current study which in investigating the effects of endurance exercise and high fat diet on insulin resistance, and ceramide content of SD-rats, plasma lipid (TC and TG), and insulin levels increased in high fat diet feed group beyond the regular diet feed group. This high fat diet raises the blood lipid level, and decreases the insulin sensitivity, and results in a tendency to have a higher resistance to insulin, which is also supported by existing studies [27]. However, a comparison between the two exercise groups and high fat diet group showed that insulin and glucose declined, and previous studies regarding endurance exercise showed an increase in insulin sensitivity and improved insulin resistance [28].
High fat diet increases lipid content in the liver and muscle. We are documenting that muscular lipid accumulation drives the cellular glucose-fatty acid cycle, increases lipid oxidation, decreases muscular glucose uptake, and increases insulin resistance [29]. Zierath et al. [30] reported results on two groups of FVB mice placed on a 50% high fat intake diet, one for 3-4 weeks and the other for 8 weeks, with no decrease in total muscular GLUT-4 and a decrease in the glucose transport rate. Rosholt et al. [31] performed tests on two groups of SD rats, one placed on a high carbohydrate diet, and the other placed on a high fat diet, and reported that there was no substantial difference in GLUT-4 in the liver. In this experiment, a high fat diet resulted in an increase in liver and muscular TG, and it was reported that there is no significant difference between skeletal muscule glucose transporter (GLUT-4) and general glucose transport rate.
Upon examining the effects of most of the past studies regarding muscular glucose uptake, Kahn and Pedersen [32] examined the results of an 80% high fat diet for 7 weeks, which showed a decline in the GLUT-4. Han et al. [33] reported on a high fat diet consisted of 32% hog fat over 8 weeks resulting in no influence on GLUT-4 after 4 weeks, and a decrease in the glucose transport rate after 8 weeks. This 4 week study of high fat diet and muscular GLUT-4 action is thought to be insufficient to observe the glucose transport rate changes, and further study considering more accurate setting of high fat intake contents, intake period, are required. Although there was such limitation, we observed increased GLUT-4 expression and glucose transport rate in two exercise groups, which is consistent with previous studies showing exercise decreased muscular insulin resistance [34-36].
Recent studies report LCACoAs, DAG, and ceramide as major metabolites which causes increasing muscular insulin resistance [1,6]. We observed that muscular lipid accumulation and diverse lipids caused by a high fat diet interrupted insulin signal transduction and GLUT-4 translocation [9,37], especially muscular lipid accumulation suppressed sphingomyelinase activity and increased muscular sphingomyelin concentration, and ceramide accumulation caused an increase in insulin resistance [38].
It is known that phosphorylation and activation of protein kinase B (Akt/PKB) is suppressed by ceramide, as far as results, the effects of membrane GLUT-4 in translocation also interrupts Akt's stimulatory pathway [9]. Mullen et al. [3] reported a 4 week trial using a 60% hog fat high fat diet resulting with the fatty acid transporter of the cell membrane, cellular DAG, and ceramide increasing. However, our study showed no apparent effect on the ceramide after 4 weeks of a high fat diet. Although the 40% high fat diet for 4 weeks caused an accumulation in muscular lipid and an increase in muscular insulin resistance, it did not increase muscular ceramide, suggesting a higher fat content for longer period is needed.
Ceramide causes the hydrolysis of sphingomyelin in vivo. Both ceramide and sphingomyelin are important in the sphingomyelin-signaling pathway, and are inserted into the lysosome and endosome membranes by acidic sphingomyelinase's (aSMase) activity [39], and sphingomyelin is hydrolyzed into phorycholine and ceramide by nSMase [17]. Most previous studies have reported that intense exercise and endurance exercise decrease the concentrations of ceramide and DAG, while increasing insulin sensitivity [15-17,40]. Dobrzyn et al. [16] reported that endurance exercise decreases the concentration of muscular ceramide. Helge et al. [17] reported that trained groups and untrained groups had trivial differences in ceramide content from target, and maximum oxygen intake of the two groups was at 58% of target after a 3-hour single trial was conducted, and resulted in a decrease in the ceramide fatty content and nSMase of both groups. Our results showing exercise decreases ceramide is consistent previous studies [16,17]. The present study, both exercise groups showed a significant decrease in the ceramide content compared to the high fat diet group.
To summarize this study, a high fat diet could significantly increase plasma lipid levels as well as in the liver and muscles, but insulin resistance markers including ceramide, GLUT-4, and muscular glucose uptake were not affected. Since, the endurance exercise group had improved GLUT-4, glucose transport rate, and muscular ceramide levels for 4 weeks compared to the non-exercising group, we can suggest the skeletal muscle insulin resistance was improved by endurance exercise. Therefore, endurance exercise could be helpful to improve the skeletal muscle insulin resistance which were developed from physical inactivity or high fat diet habits.
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