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Diabetes 50:241-247, 2001
© 2001 by the American Diabetes Association, Inc.

Nitric Oxide Increases Glucose Uptake Through a Mechanism That Is Distinct From the Insulin and Contraction Pathways in Rat Skeletal Muscle

Yasuki Higaki, Michael F. Hirshman, Nobuharu Fujii, and Laurie J. Goodyear

From the Research Division, Joslin Diabetes Center; Department of Medicine, Brigham and Women's Hospital; and Harvard Medical School, Boston, Massachusetts.

Address correspondence and reprint requests to Laurie J. Goodyear, PhD, Research Division, Joslin Diabetes Center, 1 Joslin Place, Boston, MA 02215. E-mail: laurie.goodyear{at}joslin.harvard.edu .


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Insulin, contraction, and the nitric oxide (NO) donor, sodium nitroprusside (SNP), all increase glucose transport in skeletal muscle. Some reports suggest that NO is a critical mediator of insulin- and/or contraction-stimulated transport. To determine if the mechanism leading to NO-stimulated glucose uptake is similar to the insulin- or contraction-dependent signaling pathways, isolated soleus and extensor digitorum longus (EDL) muscles from rats were treated with various combinations of SNP (maximum 10 mmol/l), insulin (maximum 50 mU/ml), electrical stimulation to produce contractions (maximum 10 min), wortmannin (100 nmol/l), and/or the NO synthase (NOS) inhibitor NG-monomethyl-L-arginine (L-NMMA) (0.1 mmol/l). The combinations of SNP plus insulin and SNP plus contraction both had fully additive effects on 2-deoxyglucose uptake. Wortmannin completely inhibited insulinstimulated glucose transport and only slightly inhibited SNP-stimulated 2-deoxyglucose uptake, whereas L-NMMA did not inhibit contraction-stimulated 2-deoxyglucose uptake. SNP significantly increased the activity of the {alpha}1 catalytic subunit of 5' AMP-activated protein kinase (AMPK), a signaling molecule that has been implicated in mediating glucose transport in fuel-depleted cells. Addition of the NOS inhibitor NG-nitro-L-arginine methyl ester (L-NAME) (1 mg/ml) to the drinking water of rats for 2 days failed to affect the increase in muscle 2-deoxyglucose uptake in response to treadmill exercise. These data suggest that NO stimulates glucose uptake through a mechanism that is distinct from both the insulin and contraction signaling pathways.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
RESEARCH DESIGN AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Nitric oxide (NO) is produced in a variety of tissues; this occurs through the activation of different isoforms of NO synthase (NOS) (1). Of the three members of the NOS family that have been identified, neuronal NOS (nNOS) and endothelial NOS (eNOS) are expressed in skeletal muscle (2). It has been reported that NO is released from isolated extensor digitorum longus (EDL) muscles incubated at rest and that prior electrical stimulation used to generate contractile activity in these muscles further increases NO release (3). Treadmill exercise can also activate NOS in gastrocnemius muscles (4), providing additional evidence that NO production in skeletal muscle increases during exercise. During the last few years, it has been proposed that NO mediates exercise-stimulated glucose transport in skeletal muscle (5,6). Exogenously administered NO, which is generated from the NO donor, sodium nitroprusside (SNP), stimulates glucose transport in isolated skeletal muscles (6,7,8) by increasing GLUT4 levels at the cell surface (8). In studies in which rats were first exercised on a treadmill (5) or had hindlimb muscles contracted via nerve stimulation (6) followed by isolation of muscles and measurement of glucose transport, data have shown that NOS inhibition blocked exercise/contraction-stimulated glucose transport. In contrast, another study has shown that when muscles are isolated and then contracted in vitro in the presence of a NOS inhibitor, there is normal activation of contraction-stimulated glucose transport (8), suggesting that there are differences between in vivo and in vitro muscle stimulation.

Insulin is a potent stimulator of glucose transport in skeletal muscle. Part of the mechanism by which insulin increases glucose transport in vivo involves enhanced blood flow and glucose delivery to the muscle, a process mediated by the release of NO from the endothelium (9,10,11). The acute administration of the NOS inhibitors NG-monomethyl-L-arginine (L-NMMA) or NG-nitro-L-arginine methyl ester (L-NAME) results in the development of marked insulin resistance, hypertension, and/or hyperglycemia (9,12,13). NOS blockade decreases blood flow to skeletal muscle and impairs insulin-mediated glucose disposal during a hyperinsulinemic-euglycemic clamp in vivo (9,12). In contrast to the effects of NOS inhibition in vivo, NOS inhibitors fail to affect insulin-stimulated glucose transport in isolated muscles incubated using in vitro preparations (6,8,9); this suggests that hemodynamic factors are needed to fully amplify the increase in insulin-stimulated glucose transport in skeletal muscle.

5'AMP-activated protein kinase (AMPK) has recently emerged as a putative regulator of multiple metabolic processes in skeletal muscle, including fatty acid and carbohydrate metabolism (14,15,16,17). We (18,19) and others (20,21) have provided evidence that AMPK is an intermediary in the signaling cascade leading to contraction-stimulated glucose transport in skeletal muscle. AMPK is a heterotrimer consisting of three subunits, {alpha}, ß, and {gamma}. The {alpha} subunit contains the kinase domain and contributes to the ATP-binding site (22). Of the two isoforms of the {alpha} subunits, {alpha}1 AMPK is widely expressed in liver, pancreas, adipose tissue, and skeletal muscle, whereas {alpha}2 AMPK catalytic isoform is predominantly expressed in skeletal muscle (23,24). Interestingly, AMPK co-immunoprecipitates with eNOS in rat cardiac muscle, and presently there are data showing that AMPK can phosphorylate eNOS in an vitro assay (25). However, it is unknown whether there is an interaction between NO and AMPK signaling to stimulate glucose transport in skeletal muscle.

In the current study, we determined if the signaling mechanism leading to NO-stimulated glucose transport is similar to, or distinct from, the signaling mechanisms leading to insulin- and contraction-stimulated glucose transport in rat skeletal muscle. Our results demonstrate that NO signaling to glucose transport is independent of the mechanisms through which insulin and muscle contraction increase transport. Furthermore, our data demonstrate that NO-stimulated glucose uptake is associated with an activation of the {alpha}1 catalytic subunit of AMPK.


   RESEARCH DESIGN AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Male Sprague-Dawley rats weighing ~40 g were purchased from Taconic Farms. Animals were housed in an animal room maintained at 23°C with a 12-h light/dark cycle and fed standard laboratory diet and water ad libitum. All protocols for animal use and euthanasia were reviewed and approved by the Institutional Animal Care and Use Committee of the Joslin Diabetes Center and accorded with NIH guidelines.

Materials. SNP, wortmannin, L-NAME, LY-83583, D-glucose, mannitol, and pyruvic acid were purchased from Sigma Chemical (St. Louis, MO). L-NMMA was purchased from Calbiochem (San Diego, CA), and 2-deoxy-D-[1,2-3H]glucose and D-[14C]mannitol were purchased from New England Nuclear (Boston, MA).

Muscle incubations. Rats were fed ad libitum before muscle isolation, and experiments commenced between 9:00 and 10:00 A.M.. Animals were killed by decapitation, and the EDL muscles were rapidly dissected. Both ends of each muscle were tied with suture (silk 4-0) and mounted on an incubation apparatus as previously described (18). The buffers were continuously gassed with 95% O2:5% CO2. Muscles were preincubated in 6 ml Krebs-Ringer bicarbonate buffer (KRBB) containing 2 mmol/l pyruvate at 37°C for 50 min in the presence or absence of SNP (1, 5, 10, or 20 mmol/l) or insulin (50 mU/ml). For contraction treatment, muscles were stimulated during the last 10 min of the 50-min incubation period (train rate 2/min, train duration 10 s, rate 100 pulses/s, duration 0.1 ms, 100 V). When added, the inhibitors wortmannin (100 nmol/l), LY-83583 (10 µmol/l), and L-NMMA (0.1 mmol/l) were present throughout the entire incubation and present >=30 min before stimulation. In preliminary experiments, dose-dependent inhibition of L-NMMA on NOS activity was measured in EDL muscle using the method previously described by Roy et al. (9). Altogether, 1 µmol/l L-NMMA inhibited NOS activity ~50%, 10 µmol/l inhibited NOS activity ~85%, and 0.1 mmol/l L-NMMA (the dose we used in the current experiments) inhibited NOS activity ~90%. Then, muscles were immediately used for the measurement of 2-deoxyglucose uptake or were immediately frozen in liquid nitrogen and subsequently analyzed for the measurement of ATP, creatine phosphate, and glycogen concentrations and isoform-specific AMPK activity.

2-Deoxyglucose uptake. The 2-deoxyglucose uptake was measured in 2 ml KRBB containing 1 mmol/l 2-deoxy-D[1,2-3H]glucose (1.5 µCi/ml) and 7 mmol/l D-[14C]mannitol (0.45 µCi/ml) (New England Nuclear, Boston, MA) at 30°C for 10 min. SNP, insulin, wortmannin, LY83583, and L-NMMA were added to the buffer if they were present during the previous incubation period. Muscles were processed, radioactivity was determined by liquid scintillation counting for dual labels, and 2-deoxyglucose uptake was calculated as previously described (26).

Assays for muscle enzymes and metabolites. To measure ATP and creatine phosphate concentrations, frozen muscles were homogenized in HClO4 in an ethanol-solid CO2 bath and centrifuged at 14,000g for 10 min at -5°C. The supernatant of the homogenates was neutralized with a solution of 2N KOH, 0.4 mol/l imidazole, and 0.4 mol/l KCl and then centrifuged at 14,000g at -9°C. The supernatant was collected and analyzed enzymatically for ATP and creatine phosphate (27).

For measurement of muscle glycogen, muscles were dissolved in 30% KOH and 5% Na2SO4 at 70°C for 15 min. Glycogen was then precipitated by mixing with 3 x volume of absolute alcohol and stored overnight at -20°C. The precipitates were collected by centrifugation at 13,000g for 5 min. The glycogen was hydrolyzed in 6N H2SO4 at 100°C for 45 min and cooled. Samples were neutralized with 1N NaOH and glucose was measured using the glucose (HK) reagent (Sigma Chemical).

For the measurement of isoform-specific AMPK activity, muscles were homogenized in ice-cold lysis buffer (1:100, wt/vol) containing 20 mmol/l Tris-HCl (pH 7.4), 1% Triton X-100, 50 mmol/l NaCl, 250 mmol/l sucrose, 50 mmol/l NaF, 5 mmol/l sodium pyrophosphate, 2 mmol/l dithiothreitol, 4 mg/l leupeptin, 50 mg/l trypsin inhibitor, 0.1 mmol/l benzamidine, and 0.5 mmol/l phenylmethylsulfonyl fluoride, and centrifuged at 14,000g for 20 min at 4°C. The supernatants (200 µg protein) were immunoprecipitated with isoform-specific antibodies to the {alpha}1 or {alpha}2 catalytic subunits of AMPK and protein A/G beads. These are anti-peptide antibodies made to the amino acid sequences DFYLATSPPDSFLDDHHLTR (339-358) of {alpha}1 and MDDSAMHIPPGLKPH (352-366) of {alpha}2. Immunoprecipitates were washed twice in both lysis buffer and in wash buffer (240 mmol/l HEPES and 480 mmol/l NaCl). Kinase reactions were performed in 40 mmol/l HEPES (pH 7.0), 0.2 mmol/l SAMS peptide (synthetic substrate for AMPK), 0.2 mmol/l AMP, 80 mmol/l NaCl, 0.8 mmol/l dithiothreitol, 5 mmol/l MgCl2, 0.2 mmol/l ATP (2 µCi [{gamma}-32P]ATP), and in a final volume of 40 µl for 20 min at 30°C (28). At the end of the reaction, a 20-µl aliquot was removed and spotted on What-man P81 paper. The papers were washed six times in 1% phosphoric acid and once with acetone. 32P incorporation was quantitated with a scintillation counter, and kinase activity was expressed as fold increases compared with basal samples.

In situ contraction studies. Rats were fed ad libitum before muscle isolation. Animals were anesthetized with an intraperitoneal injection of pentobarbital (50 mg/kg body wt). The sciatic nerve was dissected free and connected to subminiature electrodes (Harvard Apparatus, South Natick, MA). A pin under the patella tendon fixed the knee of the leg, and a 100-g weight was attached by a wire around the Achilles' tendon. The sciatic nerve was stimulated for two 5-min periods (train rate 1/s, train duration 500 ms, rate 100 pulses/s, duration 0.1 ms, 3-10 V) separated by 1 min of rest. Immediately after stimulation, EDL muscles were dissected and incubated in 3 ml KRBB containing 8 mmol/l mannitol for 20 min in the absence of presence of L-NMMA. After this incubation period, 2-deoxyglucose uptake was measured as previously described.

Treadmill exercise studies in L-NAME-treated animals. Rats were accustomed to a rodent treadmill (Quinton Instruments, Seattle, WA) for 5 min/day for 2 days before the experiment. L-NAME was added to the drinking water (1 mg/ml), and the water was changed daily for 2 days before the experiment. Systolic blood pressure was measured by a volume-oscillometric method (UR-5000; Ueda, Tokyo) before and during the 2-day L-NAME treatment. Rats ran on a rodent treadmill with a 10% incline for 1 h at 0.7 mph. Animals were killed immediately after exercise, and both the soleus and EDL muscles were rapidly dissected and mounted on the incubation apparatus. The muscles were incubated for 20 min in KRBB containing 8 mmol/l D-mannitol at 30°C, and 2-deoxyglucose uptake was measured as previously described.

Statistical analysis. Data are means ± SE. The effect of SNP on 2-deoxyglucose uptake, ATP, creatine phosphate, and isoform-specific AMPK activity was compared by a one-way analysis of variance with Fisher's protected least significant difference test. For comparison of two means, an unpaired Student's t test was performed.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Effect of SNP on glucose uptake in isolated EDL muscles. SNP resulted in a dose-dependent increase in 2-deoxyglucose uptake in isolated EDL muscles (Fig. 1). The maximal increase was twofold over basal levels at a concentration of 10 mmol/l SNP and did not increase further with 20 mmol/l SNP.



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  		FIG. 1. SNP-stimulated glucose uptake in isolated EDL muscle. 2-Deoxyglucose uptake was measured in the absence or presence of 1, 5, 10, and 20 mmol/l SNP as described in RESEARCH DESIGN AND METHODS. Data are means ± SE. **P < 0.01 vs. basal; n = 4-20 per group.

 

SNP stimulates glucose uptake through an insulin-independent pathway in isolated EDL muscles. To determine whether the combination of SNP and a maximally effective dose of insulin has additive effects on skeletal muscle glucose uptake, isolated EDL muscles were incubated in KRBB in the absence or presence of insulin and/or 10 mmol/l SNP. Figure 2A shows that the combination of SNP and insulin had nearly full additive effects on 2-deoxyglucose uptake. To determine whether SNP and insulin stimulate glucose uptake by different signaling mechanisms, isolated muscles were incubated in the presence or absence of the phosphatidylinositol 3-kinase (PI3K) inhibitor, wortmannin (100 nmol/l), before stimulation and throughout the remainder of the study (Fig. 3). As we (18,19) and others (29,30) have previously observed, wortmannin completely inhibited insulin-stimulated glucose uptake and had no effect on contraction-stimulated uptake. In contrast, wortmannin only partially (~35%) decreased SNP-stimulated glucose uptake. These findings suggest that at least part of the mechanism by which SNP and insulin stimulate glucose uptake is distinct.



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  		FIG. 2. Effects of SNP on insulin-stimulated 2-deoxyglucose uptake (A) and effect of SNP on contraction-stimulated 2-deoxyglucose uptake (B) in isolated EDL muscles. Data are means ± SE. **P < 0.01 vs. basal condition; n = 6-20 per group.

 


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  		FIG. 3. Effects of wortmannin (100 nmol/l) ({blacksquare}) on SNP-, insulin-, or contraction-stimulated 2-deoxyglucose uptake in isolated EDL muscles. 2-Deoxyglucose uptake was measured in the absence or presence of 10 mmol/l SNP as described in RESEARCH DESIGN AND METHODS. Data are means ± SE; n = 3-20 per group.

 
Additive effect of SNP plus contraction on glucose uptake in isolated EDL muscles. Next, we investigated whether SNP and contraction stimulate glucose uptake through the same mechanisms by determining if the combination of SNP and contraction has an additive effect on glucose uptake. Isolated EDL muscles were incubated in KRBB in the absence or presence of 10 mmol/l SNP, with or without electrical stimulation for muscle contraction. Interestingly, the combination of SNP and contraction had fully additive effects on skeletal muscle glucose uptake (Fig. 2B), suggesting different mechanisms for SNP-and contraction-stimulated glucose uptake.

To test this hypothesis further, we used the guanylate cyclase inhibitor LY-83583 that inhibits SNP-stimulated 2-deoxyglucose uptake in isolated muscles, as previously reported (7). Consequently, 10 µmol/l LY-83583 blocked SNP-stimulated 2-deoxyglucose uptake in the isolated EDL muscles, whereas the inhibitor did not block contraction-stimulated 2-deoxyglucose uptake (data not shown). However, we found that LY-83583 had nonspecific effects on skeletal muscle glucose uptake. In the presence of a low dose of the inhibitor (10 µmol/l), basal 2-deoxyglucose uptake increased twofold compared with the vehicle. In contrast, higher doses of the inhibitor (~50-250 µmol/l) induced muscle stiffness and dose-dependently decreased basal rates of 2-deoxyglucose uptake. LY-83483 at 10 µmol/l had no effect on the development of tension during contraction, whereas higher concentrations altered resting tension and significantly impaired the ability to develop tension during contraction (data not shown). Therefore, we do not believe that LY-83583 can be used to determine the role of NO in the regulation of contraction-stimulated glucose uptake in isolated muscles.

Effect of SNP on ATP, creatine phosphate, and glycogen concentrations and {alpha}1 and {alpha}2 AMPK activities in isolated EDL muscles. One report suggests that high concentrations of SNP decrease ATP and creatine phosphate concentrations in EDL muscles (6). We hypothesized that under these conditions, SNP may also increase AMPK activity, which is activated in response to cellular fuel depletion. SNP treatment of the muscles at concentrations ranging from 1-10 mmol/l did not alter ATP, creatine phosphate, or glycogen concentrations (Table 1). In contrast to the lack of effect of SNP on these muscle metabolities, SNP significantly increased {alpha}1 AMPK activity. Interestingly, SNP had no effect on {alpha}2 AMPK activity, whereas the contraction-stimulated increase in both {alpha}1 and {alpha}2 AMPK activity was significantly greater than that observed with SNP (Fig. 4). These data suggest distinct regulatory mechanisms leading to an increase in isoform-specific AMPK activity in rat skeletal muscle.


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  		TABLE 1
 


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  		FIG. 4. Effect of SNP or contraction on {alpha}1 AMPK activity (A) and {alpha}2 AMPK activity (B) in isolated EDL muscles. Data are means ± SE; *P < 0.05, **P < 0.01 vs. basal condition; n = 5-9 per group.

 

Effect of L-NMMA on 2-deoxyglucose uptake. To determine whether the NOS inhibitor L-NMMA affects basal- and contraction-stimulated glucose uptake, we first used isolated soleus and EDL muscles that were preincubated and contracted in KRBB in the absence or presence of 0.1 mmol/l L-NMMA. Contraction increased 2-deoxyglucose uptake 2.9-fold above basal in the soleus muscles and 3.8-fold above basal in the EDL muscles. L-NMMA treatment in vitro had no effect on basal or contraction—stimulated 2-deoxyglucose uptake in either the soleus or EDL muscles (Fig. 5).



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  		FIG. 5. In vitro contraction-stimulated 2-deoxyglucose uptake in the presence ({blacksquare}) or absence of L-NMMA in isolated soleus muscles (A) and EDL (B) muscles. Data are means ± SE; n = 5-8 per group.

 

Then, we contracted (or sham treated) EDL muscles in situ via sciatic nerve stimulation, removed the muscles, and incubated them in KRBB in the absence or presence of 0.1 mmol/l L-NMMA. As shown in Fig. 6, and similar to the results obtained in vitro, L-NMMA had no effect on basal- or contraction-stimulated 2-deoxyglucose uptake in the EDL muscles.



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  		FIG. 6. In situ contraction-stimulated 2-deoxyglucose uptake. Contracted EDL muscles were dissected and incubated in the presence ({blacksquare}) or absence of L-NMMA in vitro, and then 2-deoxyglucose uptake was measured. Data are means ± SE; n = 8-11 per group.

 

Effect of treadmill running on 2-deoxyglucose uptake in L-NAME—treated animals. The administration of L-NAME via the drinking water for 2 days resulted in a significant increase in systolic blood pressure from 104 ± 2 mmHg before L-NAME treatment to 132 ± 3 mmHg after 2 days of treatment (P < 0.001). L-NAME treatment had no effect on exercise tolerance, as all animals were able to complete the 60-min exercise task. Isolated soleus muscles from L-NAME—treated rats had lower basal 2-deoxyglucose uptake compared with untreated animals (Fig. 7). In contrast, 2 days of L-NAME treatment did not affect exercise—stimulated 2-deoxyglucose uptake in the soleus muscles.



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  		FIG. 7. Effect of 1-h treadmill exercise on 2-deoxyglucose uptake in isolated soleus muscle. L-NAME ({blacksquare}) was added to the drinking water of rats for 2 days before the experiment. Data are means ± SE; n = 6 per group.

 


   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
There are at least two distinct signaling cascades that stimulate glucose transport in muscle. One pathway is stimulated by insulin and insulin-like growth factor-1; based on studies using wortmannin and LY294002, PI3K is necessary for activation of glucose transport by this mechanism (29,30). Another insulin-independent pathway, often referred to as the contraction or contraction/hypoxia pathway is wortmannin insensitive and apparently PI3K-independent (31,32,33,34). The combination of insulin and contraction have additive or partially additive effects on glucose transport; this supports the hypothesis that separate signaling pathways regulate insulin-and contraction-stimulated glucose uptake. In the current study, we observed additive effects of SNP plus insulin on skeletal muscle glucose transport and found that NO-stimulated transport is only partially wortmannin inhibitable. Altogether, these findings demonstrate that the NO signaling pathway mediates skeletal muscle glucose uptake through an insulin-independent pathway. This finding is consistent with the observations of several other studies (6,8,9,35).

The administration of L-NMMA in vivo results in the development of marked insulin resistance (9,12,13) and hyperglycemia (13), suggesting an important role for NO in muscle glucose metabolism. Interestingly, these effects of NOS inhibition on insulin-mediated glucose uptake in vivo are not observed when isolated skeletal muscles are incubated with NOS inhibitors and insulin in vitro (6,8,9,35). These findings, combined with our results showing additive effects of SNP plus insulin and the partial inhibition using wortmannin, imply that NO augments insulin's effects systemically, most likely not at the level of skeletal muscle fibers.

Previous studies assessing the role of NO in exercise/contraction—stimulated glucose uptake have resulted in contrasting conclusions (5,6,8). In one report, hindlimb muscles were contracted in situ via electrical stimulation of the sciatic nerve, and the EDL muscles were isolated and used for measurement of glucose transport in the presence or absence of the NOS inhibitor L-NMMA (6). Under these conditions, the NOS inhibitor was shown to fully block contraction-stimulated glucose transport. In addition, another report showed that blocking NOS by adding L-NAME to the drinking water of rats prevented GLUT4 translocation to skeletal muscle sarcolemma and glucose transport in response to acute exercise (5). In contrast, when epitrochlearis muscles were contracted in vitro in the absence or presence of L-NMMA and glucose transport was measured, NOS inhibition had no effect on glucose transport (8). In the current study, three independent experiments were performed to assess this problem: 1) hindlimb muscles were contracted in vivo via electrical stimulation of the sciatic nerve, and then isolated EDL muscles were used for measurement of glucose uptake in the presence or absence of L-NMMA (similar to the methods of Balon and Nadler [6]); 2) isolated incubated EDL muscles were used for measurement of contraction-stimulated glucose uptake in the presence or absence of L-NMMA (similar to the methods of Etgen et al. [8]); and 3) L-NAME—treated rats performed running exercise for 1 h, and isolated soleus muscles were used for measurement of glucose uptake. For all three experiments, the NOS inhibitors failed to affect exercise or contraction-stimulated 2-deoxyglucose uptake. Furthermore, the combination of contraction and SNP had additive effects on glucose uptake. Therefore, our data are consistent with the conclusion that NO is not involved in the signaling pathway leading to contraction-stimulated glucose uptake in skeletal muscle.

We (18,19) and others (20,21) have hypothesized that AMPK is an essential intermediary in the signaling cascade leading to contraction-stimulated glucose transport in skeletal muscle. AMPK activity is increased when cells sense low fuel, acting as a "fuel gauge" and functioning to increase ATP generation under conditions of increased energy expenditure (19,36). Because one report suggested that incubation of skeletal muscle with a high concentration of SNP induces a significant decrease in ATP and creatine phosphate concentrations (6), we hypothesized that SNP would increase AMPK activity in skeletal muscle and that this might be part of the mechanism leading to the activation of glucose uptake. The {alpha}2 catalytic subunit of AMPK is highly expressed in skeletal muscle (23,24), and in contrast to electrical stimulation, which activates both {alpha}1 and {alpha}2 isoforms, only the {alpha}2 isoform has been reported to be increased by physical exercise in rats and humans (37,38). Surprisingly, a wide range of SNP concentrations did not significantly alter ATP, creatine phosphate, or glycogen concentrations in the incubated muscles, but these results were consistent with the lack of activation of the {alpha}2 catalytic subunit of AMPK. The lack of {alpha}2 AMPK activation with SNP is also consistent with distinct signaling mechanisms leading to contraction- and NO-stimulated glucose uptake.

Despite the lack of {alpha}2 activation and the lack of changes in ATP and creatine phosphate with SNP treatment, {alpha}1 AMPK activity was significantly increased in the incubated EDL muscles. These observations suggest that there are distinct mechanisms for the regulation of {alpha}1 and {alpha}2 AMPK activity in skeletal muscle. Furthermore, these observations demonstrate that these two catalytic isoforms may have different sensitivities to ATP and creatine phosphate in the intact muscle. In future studies, it will be interesting to determine if cytokines activate {alpha}1 AMPK in skeletal muscle, because cytokines are thought to modulate muscle glucose transport by increasing NO production (39).

In summary, our NOS-inhibitor data suggest that NO is not involved in the signaling pathway leading to contraction-stimulated glucose uptake in skeletal muscle and that SNP increases skeletal muscle glucose uptake through a mechanism that is distinct from the insulin- and contraction-signaling pathways. These observations suggest that there is a third signaling pathway that enhances glucose uptake in skeletal muscle. Furthermore, our data demonstrate that NO-stimulated glucose uptake is associated with an activation of the {alpha}1 catalytic subunit of AMPK.


   ACKNOWLEDGMENTS
 
This work was supported by National Institutes of Arthritis and Musculoskeletal and Skin Diseases Grants AR-45670 and AR-42238 (L.J.G.). Y.H. was supported by the Ministry of Education, Science, Sports, and Culture of Japan. N.F. was supported by a postdoctoral fellowship for research abroad from Japan Society for the Promotion of Science.


   FOOTNOTES
 
AMPK, AMP-activated protein kinase; EDL, extensor digitorum longus; eNOS, endothelial nitric oxide synthase; KRBB, Krebs-Ringer bicarbonate buffer; L-NAME, NG-nitro-L-arginine methyl ester; L-NMMA, NG-monomethyl-L-arginine; NO, nitric oxide; NOS, NO synthase; nNOS, neuronal NOS; P13K, phosphatidylinositol 3-kinase; SNP, sodium nitroprusside.

Received for publication February 4, 2000 and accepted in revised form October 24, 2000


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

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