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1.
Cells ; 8(3)2019 03 12.
Article in English | MEDLINE | ID: mdl-30871120

ABSTRACT

Mitochondrial DNA (mtDNA) replication is thought to be an integral part of exercise-training-induced mitochondrial adaptations. Thus, mtDNA level is often used as an index of mitochondrial adaptations in training studies. We investigated the hypothesis that endurance exercise training-induced mitochondrial enzymatic changes are independent of genomic dosage by studying mtDNA content in skeletal muscle in response to six weeks of knee-extensor exercise training followed by four weeks of deconditioning in one leg, comparing results to the contralateral untrained leg, in 10 healthy, untrained male volunteers. Findings were compared to citrate synthase activity, mitochondrial complex activities, and content of mitochondrial membrane markers (porin and cardiolipin). One-legged knee-extensor exercise increased endurance performance by 120%, which was accompanied by increases in power output and peak oxygen uptake of 49% and 33%, respectively (p < 0.01). Citrate synthase and mitochondrial respiratory chain complex I⁻IV activities were increased by 51% and 46⁻61%, respectively, in the trained leg (p < 0.001). Despite a substantial training-induced increase in mitochondrial activity of TCA and ETC enzymes, there was no change in mtDNA and mitochondrial inner and outer membrane markers (i.e. cardiolipin and porin). Conversely, deconditioning reduced endurance capacity by 41%, muscle citrate synthase activity by 32%, and mitochondrial complex I⁻IV activities by 29⁻36% (p < 0.05), without any change in mtDNA and porin and cardiolipin content in the previously trained leg. The findings demonstrate that the adaptations in mitochondrial enzymatic activity after aerobic endurance exercise training and the opposite effects of deconditioning are independent of changes in the number of mitochondrial genomes, and likely relate to changes in the rate of transcription of mtDNA.


Subject(s)
Adaptation, Physiological/genetics , Exercise/physiology , Gene Dosage , Mitochondria/enzymology , Mitochondria/genetics , Muscle, Skeletal/physiology , Cardiolipins/metabolism , DNA, Mitochondrial/genetics , Humans , Male , Muscle, Skeletal/anatomy & histology , Oxygen Consumption/physiology , Porins/metabolism , Young Adult
2.
J Clin Endocrinol Metab ; 104(5): 1841-1854, 2019 05 01.
Article in English | MEDLINE | ID: mdl-30544235

ABSTRACT

CONTEXT: Skeletal muscle molecular mechanisms underlying insulin resistance in women with polycystic ovary syndrome (PCOS) are poorly understood. OBJECTIVE: To provide insight into mechanisms regulating skeletal muscle insulin resistance in women who are lean with PCOS. PARTICIPANTS AND METHODS: A hyperinsulinemic-euglycemic clamp with skeletal muscle biopsies was performed. Thirteen women who are lean who have hyperandrogenism and PCOS and seven age- and body mass index-matched healthy control subjects were enrolled. Skeletal muscle protein expression and phosphorylation were analyzed by Western blotting and intramuscular lipid content was measured by thin-layer chromatography. RESULTS: Women with PCOS had 25% lower whole-body insulin sensitivity and 40% lower plasma adiponectin concentration than in control subjects. Intramuscular triacylglycerol, sn-1.3 diacylglycerol, and ceramide contents in skeletal muscle were higher (40%, 50%, and 300%, respectively) in women with PCOS than in control subjects. Activation of insulin signaling did not differ between groups. In women with PCOS, the insulin-stimulated glucose oxidation was reduced and insulin-stimulated dephosphorylation of pyruvate dehydrogenase (PDH) Ser293 was absent. AMP-activated protein kinase (AMPK) α2 protein expression and basal Thr172 phosphorylation were 45% and 50% lower in women with PCOS than in control subjects, respectively. CONCLUSIONS: Whole-body insulin resistance in women who are lean who have hyperandrogenism and PCOS was not related to changes in the proximal part of the insulin signaling cascade in skeletal muscle despite lipid accumulation. Rather, reduced insulin sensitivity was potentially related to plasma adiponectin levels playing a modulating role in human skeletal muscle via AMPK. Furthermore, abnormal PDH regulation may contribute to reduced whole-body metabolic flexibility and thereby insulin resistance.


Subject(s)
Hyperandrogenism/physiopathology , Insulin Resistance , Insulin/metabolism , Muscle, Skeletal/physiopathology , Polycystic Ovary Syndrome/physiopathology , Thinness/physiopathology , AMP-Activated Protein Kinases/metabolism , Adiponectin/metabolism , Adult , Biomarkers/metabolism , Body Mass Index , Case-Control Studies , Female , Follow-Up Studies , Glucose Clamp Technique , Humans , Ketone Oxidoreductases/metabolism , Male , Phosphorylation , Prognosis
3.
Diabetes ; 66(10): 2583-2595, 2017 10.
Article in English | MEDLINE | ID: mdl-28768703

ABSTRACT

To understand the mechanisms in lipid-induced insulin resistance, a more physiological approach is to enhance fatty acid (FA) availability through the diet. Nine healthy men ingested two hypercaloric diets (in 75% excess of habitual caloric intake) for 3 days, enriched in unsaturated FA (78 energy % [E%] fat) (UNSAT) or carbohydrates (80 E% carbohydrate) (CHO) as well as a eucaloric control diet (CON). Compared with CON, the UNSAT diet reduced whole-body and leg glucose disposal during a hyperinsulinemic-euglycemic clamp, while decreasing hepatic glucose production. In muscle, diacylglycerol (DAG) and intramyocellular triacylglycerol were increased. The accumulated DAG was sn-1,3 DAG, which is known not to activate PKC, and insulin signaling was intact. UNSAT decreased PDH-E1α protein content and increased inhibitory PDH-E1α Ser300 phosphorylation and FA oxidation. CHO increased whole-body and leg insulin sensitivity, while increasing hepatic glucose production. After CHO, muscle PDH-E1α Ser300 phosphorylation was decreased, and glucose oxidation increased. After UNSAT, but not CHO, muscle glucose-6-phosphate content was 103% higher compared with CON during the clamp. Thus, PDH-E1α expression and covalent regulation, and hence the tricarboxylic acid cycle influx of pyruvate-derived acetyl-CoA relative to ß-oxidation-derived acetyl-CoA, are suggested to impact on insulin-stimulated glucose uptake. Taken together, the oxidative metabolic fluxes of glucose and FA are powerful and opposite regulators of insulin action in muscle.


Subject(s)
Carbohydrate Metabolism/physiology , Dietary Fats/adverse effects , Insulin Resistance/physiology , Adult , Citric Acid Cycle/genetics , Citric Acid Cycle/physiology , Diglycerides/metabolism , Fatty Acids/blood , Fatty Acids/metabolism , Humans , Liver/metabolism , Male , Muscle, Skeletal/metabolism , Oxidation-Reduction , Phosphorylation/genetics , Phosphorylation/physiology , Pyruvate Dehydrogenase (Lipoamide)/genetics , Pyruvate Dehydrogenase (Lipoamide)/metabolism , Triglycerides/metabolism , Young Adult
4.
J Appl Physiol (1985) ; 114(5): 592-601, 2013 Mar 01.
Article in English | MEDLINE | ID: mdl-23305978

ABSTRACT

Adiponectin is an adipokine that regulates metabolism and increases insulin sensitivity. Mechanisms behind this insulin-sensitizing effect have been investigated in rodents, but little is known in humans, especially in skeletal muscle. Women have higher serum concentrations of adiponectin than men and are generally more insulin sensitive in skeletal muscle than men. We show here that large differences exist between men and women with regard to apparent adiponectin regulation of insulin-stimulated glucose uptake in skeletal muscle. Serum adiponectin was significantly associated with leg glucose uptake in healthy, young, lean men, but the association was absent in women. In addition, serum adiponectin was significantly associated with AMP-activated protein kinase (AMPK) phosphorylation in skeletal muscles of men but not in women. Serum adiponectin was also significantly, negatively associated with skeletal muscle ceramide content in men only, and interestingly, ceramide content was negatively associated with adiponectin receptor 1 (AdipoR1) expression in skeletal muscles of men. Women had lower AdipoR1 expression in skeletal muscle and a lower percentage of glycolytic adiponectin-sensitive type 2 muscle fibers than men. These associations suggest that the insulin-sensitizing effect of adiponectin on human male skeletal muscles may be mediated via AdipoR1 to activation of AMPK, leading to lowering of ceramide content. The lower skeletal muscle AdipoR1 protein expression and lower expression of adiponectin-sensitive type 2 muscle fibers in women than in men may explain the apparent lesser sensitivity to adiponectin in women.


Subject(s)
AMP-Activated Protein Kinases/metabolism , Adiponectin/blood , Ceramides/metabolism , Insulin Resistance/physiology , Muscle, Skeletal/metabolism , Adiponectin/metabolism , Adult , Cytokines/metabolism , Female , Glucose/metabolism , Humans , Insulin/metabolism , Lipid Metabolism , Male , Phosphorylation , Receptors, Adiponectin/metabolism , Regional Blood Flow , Sex Factors , Young Adult
5.
Diabetes ; 61(11): 2743-52, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22851577

ABSTRACT

Excess lipid availability causes insulin resistance. We examined the effect of acute exercise on lipid-induced insulin resistance and TBC1 domain family member 1/4 (TBCD1/4)-related signaling in skeletal muscle. In eight healthy young male subjects, 1 h of one-legged knee-extensor exercise was followed by 7 h of saline or intralipid infusion. During the last 2 h, a hyperinsulinemic-euglycemic clamp was performed. Femoral catheterization and analysis of biopsy specimens enabled measurements of leg substrate balance and muscle signaling. Each subject underwent two experimental trials, differing only by saline or intralipid infusion. Glucose infusion rate and leg glucose uptake was decreased by intralipid. Insulin-stimulated glucose uptake was higher in the prior exercised leg in the saline and the lipid trials. In the lipid trial, prior exercise normalized insulin-stimulated glucose uptake to the level observed in the resting control leg in the saline trial. Insulin increased phosphorylation of TBC1D1/4. Whereas prior exercise enhanced TBC1D4 phosphorylation on all investigated sites compared with the rested leg, intralipid impaired TBC1D4 S341 phosphorylation compared with the control trial. Intralipid enhanced pyruvate dehydrogenase (PDH) phosphorylation and lactate release. Prior exercise led to higher PDH phosphorylation and activation of glycogen synthase compared with resting control. In conclusion, lipid-induced insulin resistance in skeletal muscle was associated with impaired TBC1D4 S341 and elevated PDH phosphorylation. The prophylactic effect of exercise on lipid-induced insulin resistance may involve augmented TBC1D4 signaling and glycogen synthase activation.


Subject(s)
Exercise , Fat Emulsions, Intravenous/adverse effects , GTPase-Activating Proteins/metabolism , Insulin Resistance , Muscle, Skeletal/metabolism , Phospholipids/adverse effects , Signal Transduction , Soybean Oil/adverse effects , Adult , Emulsions/adverse effects , Glucose/administration & dosage , Glucose/metabolism , Glycogen Synthase/metabolism , Humans , Hypoglycemic Agents/pharmacology , Insulin/pharmacology , Insulin, Regular, Pork , Lactic Acid/metabolism , Leg , Male , Phosphorylation/drug effects , Protein Processing, Post-Translational/drug effects , Pyruvate Dehydrogenase Complex/metabolism , Signal Transduction/drug effects
6.
Diabetes ; 60(1): 64-73, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20956497

ABSTRACT

OBJECTIVE: We have previously shown that overnight fasted women have higher insulin-stimulated whole body and leg glucose uptake despite a higher intramyocellular triacylglycerol concentration than men. Women also express higher muscle mRNA levels of proteins related to lipid metabolism than men. We therefore hypothesized that women would be less prone to lipid-induced insulin resistance. RESEARCH DESIGN AND METHODS: Insulin sensitivity of whole-body and leg glucose disposal was studied in 16 young well-matched healthy men and women infused with intralipid or saline for 7 h. Muscle biopsies were obtained before and during a euglycemic-hyperinsulinemic clamp (1.42 mU · kg⁻¹ · min⁻¹). RESULTS: Intralipid infusion reduced whole-body glucose infusion rate by 26% in women and 38% in men (P < 0.05), and insulin-stimulated leg glucose uptake was reduced significantly less in women (45%) than men (60%) after intralipid infusion. Hepatic glucose production was decreased during the clamp similarly in women and men irrespective of intralipid infusion. Intralipid did not impair insulin or AMPK signaling in muscle and subcutaneous fat, did not cause accumulation of muscle lipid intermediates, and did not impair insulin-stimulated glycogen synthase activity in muscle or increase plasma concentrations of inflammatory cytokines. In vitro glucose transport in giant sarcolemmal vesicles was not decreased by acute exposure to fatty acids. Leg lactate release was increased and respiratory exchange ratio was decreased by intralipid. CONCLUSIONS: Intralipid infusion causes less insulin resistance of muscle glucose uptake in women than in men. This insulin resistance is not due to decreased canonical insulin signaling, accumulation of lipid intermediates, inflammation, or direct inhibition of GLUT activity. Rather, a higher leg lactate release and lower glucose oxidation with intralipid infusion may suggest a metabolic feedback regulation of glucose metabolism.


Subject(s)
Insulin Resistance/physiology , Insulin/physiology , Lipids/pharmacology , Phospholipids/pharmacology , Signal Transduction/physiology , Soybean Oil/pharmacology , Triglycerides/metabolism , Adiponectin/blood , Adipose Tissue/anatomy & histology , Adult , Animals , Basal Metabolism/physiology , Blood Flow Velocity , Body Height , Body Mass Index , Emulsions/pharmacology , Epinephrine/blood , Estradiol/blood , Exercise , Fasting , Female , Glucose/metabolism , Glucose Clamp Technique , Humans , Inflammation/physiopathology , Inflammation/prevention & control , Insulin/blood , Insulin/pharmacology , Male , Muscle, Skeletal/cytology , Norepinephrine/blood , Oxygen Consumption , Rats , Sarcolemma/metabolism , Sex Characteristics , Triglycerides/blood
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