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Departments of Medicine (B.H.G., J.H., D.E.K.) and Cell Biology (S.W.), University of Pittsburgh, Pittsburgh, Pennsylvania 15261
Address all correspondence and requests for reprints to: Dr. Bret H. Goodpaster, E1140 Biomedical Science Tower, University of Pittsburgh, Pittsburgh, Pennsylvania 15261. E-mail: bgood+{at}pitt.edu
Abstract
We examined the hypothesis that an excess accumulation of intramuscular lipid (IMCL) is associated with insulin resistance and that this may be mediated by the oxidative capacity of muscle. Nine sedentary lean (L) and 11 obese (O) subjects, 8 obese subjects with type 2 diabetes mellitus (D), and 9 lean, exercise-trained (T) subjects volunteered for this study. Insulin sensitivity (M) determined during a hyperinsulinemic (40 mU·m-2min-1) euglycemic clamp was greater (P < 0.01) in L and T, compared with O and D (9.45 ± 0.59 and 10.26 ± 0.78 vs. 5.51 ± 0.61 and 1.15 ± 0.83 mg·min-1kg fat free mass-1, respectively). IMCL in percutaneous vastus lateralis biopsy specimens by quantitative image analysis of Oil Red O staining was approximately 2-fold higher in D than in L (3.04 ± 0.39 vs. 1.40 ± 0.28% area as lipid; P < 0.01). IMCL was also higher in T (2.36 ± 0.37), compared with L (P < 0.01). The oxidative capacity of muscle determined with succinate dehydrogenase staining of muscle fibers was higher in T, compared with L, O, and D (50.0 ± 4.4, 36.1 ± 4.4, 29.7 ± 3.8, and 33.4 ± 4.7 optical density units, respectively; P < 0.01). IMCL was negatively associated with M (r = -0.57, P < 0.05) when endurance-trained subjects were excluded from the analysis, and this association was independent of body mass index. However, the relationship between IMCL and M was not significant when trained individuals were included. There was a positive association between the oxidative capacity and M among nondiabetics (r = 0.37, P < 0.05). In summary, skeletal muscle of trained endurance athletes is markedly insulin sensitive and has a high oxidative capacity, despite having an elevated lipid content. In conclusion, the capacity for lipid oxidation may be an important mediator of the association between excess muscle lipid accumulation and insulin resistance.
RECENT EVIDENCE SUGGESTS that an excess accumulation of skeletal muscle lipid is associated with insulin resistance in human obesity (1, 2, 3, 4, 5, 6) and in type 2 diabetes mellitus (DM) (7, 8). Animal models of insulin resistance also lend support to this concept (9, 10, 11). Typically, muscle triglyceride (TG) concentrations have been measured using biochemical extraction methods in homogenates from either percutaneous biopsies or whole muscle (4, 5, 7, 8, 10). Thus, it is not certain whether the increased muscle TG concentrations were confounded by contamination from adipose tissue. Recent studies (1, 3, 6, 12, 13) using magnetic resonance spectroscopy (MRS) have also found that intramyocellular lipid is negatively associated with insulin sensitivity in vivo, although absolute concentrations of lipid using this methodology has yet to be quantified. Our group has recently demonstrated, using quantitative histochemistry, that the lipid contained within muscle fibers from obese subjects with type 2 DM was higher, compared with lean nondiabetics (14). Therefore, one hypothesis tested in the current study was that an excess accumulation of lipid within muscle fibers is associated with insulin resistance independent of obesity.
Insulin resistant skeletal muscle is characterized by lower oxidative capacity (15, 16) and lower postabsorptive rates of fatty acid oxidation (17). Elevated concentrations of lipid contained within skeletal muscle have also been linked to an impaired oxidative capacity of muscle (15) and lower rates of fatty acid oxidation by muscle (17). This raises the possibility that the association between lipid accumulation within muscle and insulin resistance is influenced by a lower capacity for the oxidation of lipid as an energy substrate.
Exercise training enhances insulin sensitivity (18, 19, 20, 21) and the capacity for lipid oxidation (5, 22, 23, 24). Exercise training also increases fatty acid oxidation from intramuscular TG stores during exercise (25). However, the effect of exercise training on intramuscular TG is equivocal; some studies have demonstrated that training increases intramuscular TG (26, 27), and others have shown a decrease with exercise training (28). Accumulation of TG within skeletal muscle may not be invariably linked to insulin resistance. The possibility that endurance-trained athletes have an enhanced storage of intramuscular TG despite their high insulin sensitivity within muscle would contradict the apparent general association between increased intramuscular TG and insulin resistance. This serves as the basis for the intriguing hypothesis that the capacity for oxidative metabolism is an important mediator in the association between intramuscular lipid and insulin resistance.
Experimental Subjects
Nine lean and 8 obese volunteers with type 2 DM, 11 obese nondiabetics, and 9 endurance-trained athletes between the ages of 25 and 50 yr were recruited by public advertisement. Before participation, all potential research volunteers underwent a medical screening evaluation before participation. All volunteers were normotensive and had fasting TG and cholesterol levels less than 300 mg/dl without any antihypertensive or lipid-lowering medications. Women taking oral contraceptives were also excluded. Type 2 DM volunteers had been withdrawn from oral antidiabetic medications for at least 2 wk before this study, and none had received insulin. Type 2 DM patients were excluded if they had moderate to severe complications of DM such as retinopathy or peripheral neuropathy. None of the lean, obese nondiabetic individuals or those with type 2 DM were currently engaged in exercise training, and all were weight stable (±2 kg) for at least 3 months before enrollment in the study. The endurance-trained individuals were currently participating in a minimum of 5 d/wk of aerobic exercise training, and all but two were involved in competitive cycling. The study was approved by the University of Pittsburgh Institutional Review Board, and informed written consent was obtained from each volunteer.
Materials and Methods
Muscle biopsies
Subjects were instructed not to perform physical exercise 48 h before the muscle biopsy procedure to help prevent acute effects of exercise on muscle TG. Subjects were given a standard 10 kcal/kg meal consisting of 50% carbohydrate, 30% fat, and 20% protein the night before the biopsy and then fasted overnight.
Muscle biopsies were obtained from the middle region of the vastus lateralis muscle (15 cm above the patella) and approximately 2 cm away from the fascia by the percutaneous needle biopsy technique as described by Evans et al. (29). Muscle specimens were trimmed, mounted, and frozen in isopentane cooled at -160 C by liquid nitrogen and stored at -80 C for histochemical analysis.
Histochemical analysis
Histochemical analyses were performed on light microscopic micrographs of 8-µm-thick transverse cryostat sections at -29 C (Micron HM505E, Walldorff, Germany). Initial sections from each frozen muscle block were inspected without stain to ensure that proper cross-sectional cuts were being obtained; if not, then the orientation was adjusted and this process repeated until good cross-sectional orientation was obtained. Muscle sectioning, staining, and image analysis were done in a blinded manner with respect to group.
Lipid staining was done using the Oil Red O soluble dye, which stains
neutral lipid (mainly TGs) with an orange-red tint (30)
(Fig. 1
). The intramuscular lipid (IMCL)
content was determined as previously described (14).
Briefly, an Olympus Corp. light microscope (Provis, Tokyo,
Japan), was used to examine the stained muscle sections, using a 40x
oil immersion objective and bright field settings. Images were
digitally captured using a CCD camera (Sony, Tokyo,
Japan). Contiguous fields of view within the biopsy section that were
free from artifact were analyzed for lipid content; quantitative image
analysis was then carried out on at least 80 fibers, or approximately
10 contiguous fibers per field.
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Oxidative capacity of muscle was determined with succinate dehydrogenase (SDH) staining (31). Quantification of SDH staining was performed using image analysis of staining intensity, a method that has been verified with biochemical determination of SDH activity in muscle (32, 33). As negative control slides for this reaction, to assess background staining, sections were incubated in media without the enzyme substrate succinate. The proportion of type 1, 2a, and 2b muscle fibers was also determined on cryosections containing at least 300 fibers by ATPase staining (34).
Insulin sensitivity
Insulin sensitivity was determined using the hyperinsulinemic
(40 mU·m-2·min-1), euglycemic
clamp method as previously described (2). Subjects were
instructed to avoid strenuous activity for 2 d preceding these
studies. On the day before measurement of insulin sensitivity, subjects
were admitted to the University of Pittsburgh General Clinical Research
Center. That evening they received a standard dinner (10 kcal/kg; 50%
carbohydrate, 30% fat, 20% protein) and then fasted until completion
of the glucose and insulin infusions. At 
0700 h, a
catheter was placed in a forearm vein before beginning the euglycemic
insulin infusion (Humulin, Eli Lilly & Co., Indianapolis,
IN). An additional catheter was inserted into a heated hand vein in the
retrograde direction for sampling of arterialized blood. After
obtaining basal blood samples, a primed constant infusion of [6,
6-2H2] glucose (0.22
µmol·kg-1, 17.6
µmol·kg-1 prime) 99% enriched
(Isotech, Inc., Miamisburg, OH) was started with a
calibrated syringe pump (Harvard Apparatus, Natick, MA),
allowing 2 h for isotopic equilibration before the initiation of
the insulin infusion in only subjects with type 2 DM. Euglycemia was
maintained using an adjustable infusion of 20% dextrose, to which [6,
6-2H2] glucose was added
to maintain stable plasma glucose enrichment (35). Plasma
glucose was determined at 5-min intervals during the 4-h clamp. Blood
samples for measurement of [6,
6-2H2] glucose enrichment
were collected every 10 min during the final 40 min of insulin
infusion.
Analyses
Plasma glucose was measured using an automated glucose oxidase reaction (2300 glucose analyzer, YSI, Inc., Yellow Springs, OH). Enrichment of plasma [6, 6-2H2] glucose enrichment was determined by gas chromatography-mass spectrometry (HP 5971 MS, 5890 Series 2 GC; Hewlett Packard, Palo Alto, CA) analysis of the glucose penta-acetate derivatives, selectively monitoring ions at mass-to-charge 200 and 202.
Calculations. Rate of plasma glucose appearance and utilization were calculated using the Steele equations (36), as modified for variable rate glucose infusions, which contain isotope (35).
Statistical analysis. Data are presented as mean ± SEM, unless otherwise indicated. Group differences in IMCL, muscle oxidative staining, and insulin sensitivity were assessed with one-way ANOVA, using a Bonferroni correction for specific group comparisons. The relationships between insulin sensitivity and intramuscular lipid and muscle oxidative staining were determined with bivariate regression analysis. Stepwise multivariate regression analysis was used to determine these associations after adjusting for total adiposity. All statistics were performed using JMP version 3.1.6 for the Macintosh (SAS Institute, Inc., Cary, NC).
Results
Subject clinical characteristics
Lean and obese volunteers and obese subjects with type 2 DM were considered sedentary from their recent physical activity levels; none of these individuals were participating in regular exercise. The endurance-trained subjects were currently participating in at least 5 d/wk of aerobic exercise training. Moreover, the athletes had a relatively high aerobic capacity as evidenced by their maximal oxygen uptake of 61.0 ± 5.4 ml/kg per min, determined in another study protocol.
The general body composition characteristics of these subjects are
described in Table 1. Obese subjects with
type 2 diabetes were older than nondiabetics. Per study design, lean
sedentary and trained subjects had a lower body mass index than either
the obese or obese type 2 DM groups. Accordingly, their total and
proportion of body fat were also lower as determined by DXA, model
DPX-L (Lunar Corp., Madison, WI) using software version
1.3Z. Fasting plasma glucose was higher (P < 0.05) in
the obese subjects with type 2 DM, compared with nondiabetics, who had
similar fasting plasma glucose values (Table 2). Serum TG concentrations were
significantly lower (P < 0.05) in the trained group
(Table 2).
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Values for insulin sensitivity are represented relative to fat
free mass. Lean subjects were nearly twice as insulin sensitive,
compared with obese subjects (P < 0.05; Fig. 2). Expectedly, those with type 2 DM were
markedly insulin resistant, compared with those without diabetes
(P < 0.05). Insulin sensitivity was similar in lean
sedentary subjects and lean endurance-trained subjects.
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The content of IMCL was approximately 2-fold higher in type 2 DM,
compared with lean sedentary subjects (P < 0.05; Fig. 3). Trained subjects also had higher IMCL
than the lean untrained subjects (P < 0.05), and
indeed these values for trained subjects were similar to that of
diabetic muscle. The oxidative capacity of muscle, determined by the
SDH staining intensity, was 65% higher in trained muscle, compared
with the sedentary obese group and 50% higher than those with type 2
DM (P < 0.05 for both; Fig. 4). The oxidative capacity also tended to
be higher in trained subjects, compared with the lean sedentary group,
but this difference was not significant. The oxidative capacities of
lean, obese, and obese type 2 DM sedentary subjects were not
significantly different. Interestingly, muscle fiber type was not
different among the four groups. The proportion of type 1 fibers was
40 ± 8, 35 ± 4, 39 ± 7, and 44 ± 4 for lean,
obese, obese type 2 DM, and trained subjects, respectively. The
proportion of type 2a and 2b fibers was also not different among
groups.
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Among sedentary subjects, there was an inverse association between
the amount of lipid contained within muscle fibers (IMCL) and insulin
sensitivity (Fig. 5), in which IMCL
accounted for 32% of the variance in insulin sensitivity. This
relationship remained significant (P < 0.05) when
obese individuals with type 2 DM omitted from the analysis, though the
observed variance was reduced to 19%. Moreover, stepwise multivariate
regression revealed that the association between IMCL and insulin
resistance was independent of total adiposity and age. However, the
negative association between IMCL and insulin sensitivity was observed
only when the trained subjects were excluded from the analysis; there
was no association (r2 = 0.03) when
exercise-trained individuals were included.
|
), but only when the obese subjects with
type 2 diabetes were omitted from the analysis. The profound insulin
resistance in the diabetics likely contributed to our inability to
detect this association with these subjects included. In fact, three of
the obese subjects with diabetes had no measurable insulin-stimulated
glucose disposal. Nevertheless, this positive correlation between SDH
staining and insulin sensitivity is consistent with the higher
oxidative capacity and higher insulin sensitivity in the trained
subjects, compared with the sedentary groups.
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A primary finding of the present study was that the lipid contained within muscle fibers of sedentary individuals was inversely associated with insulin resistance. However, individuals engaged in regular exercise training had higher muscle fiber lipid content despite being markedly insulin sensitive. The higher oxidative capacity of skeletal muscle in these trained athletes provides a likely intermediary in the association between muscle lipid content and insulin resistance. By examining the muscle lipid content, oxidative capacity, and insulin sensitivity in trained and sedentary individuals, we have identified potential mediators governing the association between skeletal muscle lipid and insulin resistance of obesity and type 2 DM.
Skeletal muscle lipid within muscle fibers was directly ascertained with quantitative histochemical analysis of biopsy specimens, reflecting true intracellular concentration of lipid. Because of inherent limitations of prior methods, prior studies have relied on certain assumptions in their measurements of intramuscular TG concentrations. Quantifying intramuscular TG in human biopsy samples has typically involved the biochemical extraction of TG, possibly resulting in the inadvertent contamination of fat and connective tissue within the sample (4, 5, 7, 8, 10). Proton MRS studies of human muscle performed by several independent groups have recently differentiated extra- and intramyocellular lipid (IMCL) and have observed negative associations between IMCL and insulin sensitivity (1, 3, 6, 12, 13). Although MRS represents a novel noninvasive method to determine relative IMCL content in vivo, quantification of actual IMCL concentrations using MRS remains problematic. Nevertheless, the prior observed associations between IMCL and insulin resistance should not be discounted. On the contrary, our findings confirm those of these previous studies demonstrating that increased lipid stored within muscle fibers is indeed associated with insulin resistance.
Despite their expectedly higher insulin sensitivity, compared with obese subjects and with those with type 2 DM, the IMCL content in the trained subjects in this study was similar to individuals with type 2 DM. Moreover, the observed association between IMCL and insulin resistance disappeared when trained subjects were included in the analysis. In previous studies observing associations between IMCL and insulin resistance, the influence of physical fitness or physical activity was not directly assessed (1, 3, 4, 5, 6, 12, 13). Thus, this study represents the first examination of the potential influence of physical training on the association between IMCL and insulin resistance. Interestingly, insulin sensitivity in these athletes was not greater, compared with lean sedentary men and women. This finding is supported by other studies finding only modest or no improvements in insulin sensitivity with exercise training when the effects of weight loss (21) and the last exercise session (21, 37) are accounted for.
Although their insulin sensitivity was similar, endurance-trained athletes had nearly 2-fold higher amounts of lipid stored within their muscle fibers, compared with their lean, sedentary counterparts. This finding is in accord with Hoppeler et al. (26), who observed that the volume of lipid droplets on electron micrographs was higher in trained subjects. However, IMCL quantification in that study was confined to the ultrastructure scale, which limited the scope of quantification. Boesch and Kreis (38) found in using MRS that IMCL was higher in one trained athlete, compared with other sedentary but otherwise healthy subjects. The effects of training on IMCL have not been clear, with some studies reporting higher concentrations of IMCL after training (27, 39) and others reporting decreases (28). These disparate results are not entirely surprising given the relatively small number of studies and the relatively high interbiopsy variability in the measure of IMCL (40). With relatively short-term training studies, it is conceivable that the specific adaptation to enhance TG storage had not yet occurred during the course of the study. There also remains the possibility that the subcellular localization of lipid within muscle may impact upon the association with insulin action.
The higher IMCL content in these trained athletes raises the possibility that IMCL is merely a surrogate for other factors in muscle that may directly affect insulin-stimulated glucose metabolism. Thompson and Cooney (41) recently reported that long chain fatty acyl CoA in skeletal muscle may induce insulin resistance by inhibiting hexokinase activity. Other reports suggest that long chain CoA and diacylglycerol, metabolites of IMCL metabolism, act on insulin signaling pathways in muscle (42, 43). Thus, no direct effect of muscle TG on insulin-stimulated glucose metabolism has been defined. Moreover, periodic turnover of IMCL and its associated metabolites with regular exercise may limit their negative influence on insulin signaling. Further studies are needed to specifically examine the effects of training on these lipid metabolites within muscle and, in general, how they may play a role in insulin resistance.
Alternative mechanisms may help elucidate the reasons that these trained athletes had high IMCL concomitant with their high insulin sensitivity. Factors governing the enhanced insulin sensitivity in muscle with exercise training such as increased GLUT 4 content (44, 45) and skeletal muscle blood flow (44) may override the negative consequences of IMCL on insulin-stimulated glucose metabolism. Thus, it is likely that the upregulation of these intermediates in the trained subjects at least partially modulated any deleterious effect of increased IMCL on insulin sensitivity. In addition, we addressed the role of the oxidative capacity of muscle as a mediator of insulin sensitivity.
The oxidative capacity was higher in trained subjects in accord with prior studies (22, 23, 46, 47). This, together with the high IMCL and insulin sensitivity in these subjects, suggests that the capacity for IMCL oxidation is an important intermediary of insulin resistance. A higher oxidative capacity within muscle reflects their increased mitochondria content and enhanced capacity for lipid oxidation. Including the trained subjects in the analysis, a lower oxidative capacity was associated with insulin resistance. This is in agreement with prior studies demonstrating that skeletal muscle from insulin-resistant and obese subjects is characterized by lower oxidative capacity (15, 17) and lower fasting rates of fatty acid oxidation (17, 48, 49). As a storage depot of fatty acids, IMCLs are changeable. During moderate exercise, fatty acids from the hydrolysis of IMCL are capable of contributing a substantial portion of the energy required for oxidative metabolism (25, 50, 51). Perhaps the periodic utilization of this energy source should be considered as an important factor mediating the association between IMCL and insulin resistance. Little, if any, fatty acids from IMCL are oxidized during resting conditions (52). The deficient utilization and subsequent accumulation of IMCL in sedentary subjects may confer insulin resistance, whereas the periodic utilization of this energy substrate during regular exercise may overcome this consequence of IMCL accrual.
Recent studies in mice overexpressing uncoupling protein also provide support for the role of an increased capacity for fatty acid oxidation to mediate the potential negative influence of IMCL on insulin-stimulated glucose metabolism (53). IMCL in mice overexpressing uncoupling protein was increased despite an increase in energy expenditure, GLUT 4 content, hexokinase activity within muscle, and a decrease in overall adiposity (53). Thus, in many respects, this transgenic animal model mimics the situation observed in skeletal muscle of endurance-trained athletes in which IMCLs are higher than in sedentary individuals with similar insulin sensitivity. Lipoprotein lipase (LPL) in skeletal muscle also plays a direct role in IMCL accretion (54), and exercise increases muscle LPL (55). Thus, it is likely that the induction of muscle LPL following exercise helps to replenish IMCL following exercise (56, 57). More studies are required to demonstrate whether an elevated muscle LPL in trained athletes influences their elevated IMCL content.
In summary, the association between intramuscular lipid content and insulin resistance may be influenced by the oxidative capacity of skeletal muscle. The higher concentrations of lipid stored within muscle fibers, in conjunction with a higher oxidative capacity and insulin sensitivity of individuals participating in regular exercise, provide support for this concept. It is likely that intramuscular lipid content alone may not confer insulin resistance but rather may act as a surrogate for other potentially detrimental lipid metabolites. Future studies should examine the effects of exercise training on the interactions between fatty acid metabolism and insulin resistance of obesity and type 2 DM.
Acknowledgments
We thank the research volunteers for their participation in the study. We appreciate the skill of the nursing staff at the General Clinical Research and Obesity and Nutrition Research centers for their expert technical and analytical support.
Footnotes
This work was supported by funding from NIH Grants K01 AG00851 (to B.H.G.), R01 DK-49200-04 (to D.E.K.), 5M01RR00056 (General Clinical Research Center), and 1P30DK46204 (Obesity and Nutrition Research Center).
Abbreviations: DM, Diabetes mellitus; IMCL, intramuscular lipid; LAI, total area occupied by lipid droplets of muscle fiber; LPL, lipoprotein lipase; MRS, magnetic resonance spectroscopy; SDH, succinate dehydrogenase; TG, triglyceride.
Received February 23, 2001.
Accepted August 28, 2001.
References
may
contribute to muscle insulin resistance induced by lipid accumulation
during chronic glucose infusion in rats (Abstract). Diabetes 46:241A
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, obese •, and type 2 DM 
subjects; n = 35. The r value represents the simple correlation
coefficient for these subjects combined. The designated 
indicates
that this relationship was significant.
subjects; n = 29. The r value represents the simple
correlation coefficient for these subjects combined. The designated