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Mitochondrial dysfunction results from oxidative stress in the skeletal muscle of diet-induced insulin-resistant mice
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4615-5653-4_7openalex-snapshot
Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo
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Expression of key genes of fatty acid oxidation, including adiponectin receptors, in skeletal muscle of Type 2 diabetic patients
inferredcites →https://doi.org/10.1007/s00125-006-0170-2openalex-snapshot
Mitochondria are impaired in the adipocytes of type 2 diabetic mice
inferredcites →https://doi.org/10.1007/s001250051123openalex-snapshot
Intramyocellular lipid concentrations are correlated with insulin sensitivity in humans: a 1 H NMR spectroscopy study
inferredcites →https://doi.org/10.1016/j.cell.2006.11.013openalex-snapshot
Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α
inferredcites →https://doi.org/10.1017/s0029665107005277openalex-snapshot
High-fat diet, muscular lipotoxicity and insulin resistance
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DNA Polymerase γ in Mitochondrial DNA Replication and Repair
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Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage
inferredcites →https://doi.org/10.1038/ng1180openalex-snapshot
PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
inferredcites →https://doi.org/10.1038/sj.emboj.7601633openalex-snapshot
Metabolic control of muscle mitochondrial function and fatty acid oxidation through SIRT1/PGC‐1α
inferredcites →https://doi.org/10.1042/bj1140597openalex-snapshot
The kinetic properties of citrate synthase from rat liver mitochondria
inferredcites →https://doi.org/10.1046/j.1365-201x.2003.01162.xopenalex-snapshot
The role of intramuscular lipid in insulin resistance
inferredcites →https://doi.org/10.1056/nejmoa031314openalex-snapshot
Impaired Mitochondrial Activity in the Insulin-Resistant Offspring of Patients with Type 2 Diabetes
inferredcites →https://doi.org/10.1073/pnas.1032913100openalex-snapshot
Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1
inferredcites →https://doi.org/10.1074/jbc.274.34.24202openalex-snapshot
Ceramide Generation Is Sufficient to Account for the Inhibition of the Insulin-stimulated PKB Pathway in C2C12 Skeletal Muscle Cells Pretreated with Palmitate
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Mechanism by Which Fatty Acids Inhibit Insulin Activation of Insulin Receptor Substrate-1 (IRS-1)-associated Phosphatidylinositol 3-Kinase Activity in Muscle
inferredcites →https://doi.org/10.1074/jbc.m212754200openalex-snapshot
Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism
inferredcites →https://doi.org/10.1074/jbc.m300293200openalex-snapshot
Microarray Profiling of Human Skeletal Muscle Reveals That Insulin Regulates ∼800 Genes during a Hyperinsulinemic Clamp
inferredcites →https://doi.org/10.1079/pns2003336openalex-snapshot
The role of uncoupling protein 3 in fatty acid metabolism: protection against lipotoxicity?
inferredcites →https://doi.org/10.1089/ars.2005.7.1040openalex-snapshot
The Molecular Basis for Oxidative Stress-Induced Insulin Resistance
inferredcites →https://doi.org/10.1093/nar/gkf392openalex-snapshot
The mitochondrial DNA polymerase as a target of oxidative damage
inferredcites →https://doi.org/10.1096/fj.01-1027comopenalex-snapshot
High glucose‐induced oxidative stress and mitochondrial dysfunction in neurons
inferredcites →https://doi.org/10.1096/fj.03-1065fjeopenalex-snapshot
Triacylglycerol accumulation in human obesity and type 2 diabetes is associated with increased rates of skeletal muscle fatty acid transport and increased sarcolemmal FAT/CD36
inferredcites →https://doi.org/10.1100/tsw.2003.09openalex-snapshot
DNA Polymerase Gamma in Mitochondrial DNA Replication and Repair
inferredcites →https://doi.org/10.1126/science.1104343openalex-snapshot
Mitochondrial Dysfunction and Type 2 Diabetes
inferredcites →https://doi.org/10.1152/jappl.1997.83.1.166openalex-snapshot
Altered glycolytic and oxidative capacities of skeletal muscle contribute to insulin resistance in NIDDM
inferredcites →https://doi.org/10.1172/jci21625openalex-snapshot
Increased oxidative stress in obesity and its impact on metabolic syndrome
inferredcites →https://doi.org/10.1172/jci25151openalex-snapshot
Reduced mitochondrial density and increased IRS-1 serine phosphorylation in muscle of insulin-resistant offspring of type 2 diabetic parents
inferredcites →https://doi.org/10.1210/er.2001-0039openalex-snapshot
Oxidative Stress and Stress-Activated Signaling Pathways: A Unifying Hypothesis of Type 2 Diabetes
inferredcites →https://doi.org/10.1210/er.2002-0012openalex-snapshot
Peroxisome Proliferator-Activated Receptor-γ Coactivator 1α (PGC-1α): Transcriptional Coactivator and Metabolic Regulator
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Exogenous Leptin Increases Lipid Peroxidation in the Mouse Brain
inferredcites →https://doi.org/10.2174/0929867043455620openalex-snapshot
Nutrient-Induced Insulin Resistance in Human Skeletal Muscle
inferredcites →https://doi.org/10.2337/diabetes.48.8.1600openalex-snapshot
Intramyocellular triglyceride content is a determinant of in vivo insulin resistance in humans: a 1H-13C nuclear magnetic resonance spectroscopy assessment in offspring of type 2 diabetic parents.
inferredcites →https://doi.org/10.2337/diabetes.51.10.2944openalex-snapshot
Dysfunction of Mitochondria in Human Skeletal Muscle in Type 2 Diabetes
inferredcites →https://doi.org/10.2337/diabetes.51.5.1477openalex-snapshot
Increased Efficiency of Fatty Acid Uptake Contributes to Lipid Accumulation in Skeletal Muscle of High Fat-Fed Insulin-Resistant Rats
inferredcites →https://doi.org/10.2337/diabetes.53.9.2232openalex-snapshot
Suppressor of Cytokine Signaling 3 Expression and Insulin Resistance in Skeletal Muscle of Obese and Type 2 Diabetic Patients
inferredcites →https://doi.org/10.2337/diabetes.54.7.1926openalex-snapshot
A High-Fat Diet Coordinately Downregulates Genes Required for Mitochondrial Oxidative Phosphorylation in Skeletal Muscle
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Hyperglycemia induced expression, phosphorylation, and translocation of αB‐crystallin in rat skeletal muscle
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Role of Skeletal Muscle in Insulin Resistance and Glucose Uptake
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Effect of magnesium on reducing the UV‐induced oxidative damage in marrow mesenchymal stem cells
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Enhanced lipid—but not carbohydrate—supported mitochondrial respiration in skeletal muscle of PGC‐1α overexpressing mice
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High Insulin‐Induced Down‐Regulation of Erk‐1/IGF‐1R/FGFR‐1 Signaling Is Required for Oxidative Stress‐Mediated Apoptosis of Adipose‐Derived Stem Cells
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Brazilian green propolis improves gut microbiota dysbiosis and protects against sarcopenic obesity
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Differential effects of Western diet and traumatic muscle injury on skeletal muscle metabolic regulation in male and female mice
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Adaptations of Skeletal Muscle Mitochondria to Obesity, Exercise, and Polyunsaturated Fatty Acids
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Apigenin Ameliorates the Obesity‐Induced Skeletal Muscle Atrophy by Attenuating Mitochondrial Dysfunction in the Muscle of Obese Mice
inferred← citeshttps://doi.org/10.1002/mnfr.201700541openalex-snapshot
Phytoceuticals in Fenugreek Ameliorate VLDL Overproduction and Insulin Resistance via the Insig Signaling Pathway
inferred← citeshttps://doi.org/10.1002/mnfr.201900688openalex-snapshot
Avocatin B Protects Against Lipotoxicity and Improves Insulin Sensitivity in Diet‐Induced Obesity
inferred← citeshttps://doi.org/10.1002/oby.21081openalex-snapshot
Skeletal muscle myotubes in severe obesity exhibit altered ubiquitin‐proteasome and autophagic/lysosomal proteolytic flux
inferred← citeshttps://doi.org/10.1002/oby.21922openalex-snapshot
Metabolomic Profiling of Long‐Term Weight Change: Role of Oxidative Stress and Urate Levels in Weight Gain
inferred← citeshttps://doi.org/10.1002/pmic.201700375openalex-snapshot
Proteomics Analysis of Skeletal Muscle from Leptin‐Deficient ob/ob Mice Reveals Adaptive Remodeling of Metabolic Characteristics and Fiber Type Composition
inferred← citeshttps://doi.org/10.1007/978-1-4614-5441-0_21openalex-snapshot
Oxidative Stress in Diabetes
inferred← citeshttps://doi.org/10.1007/978-1-4939-1203-2_4openalex-snapshot
Critical Importance of the Perinatal Period in the Development of Obesity
inferred← citeshttps://doi.org/10.1007/978-3-319-55330-6_25openalex-snapshot
Insulin Resistance and Mitochondrial Dysfunction
inferred← citeshttps://doi.org/10.1007/978-3-319-55530-0_49openalex-snapshot
High-Fructose Consumption and the Epigenetics of DNA Methylation
inferred← citeshttps://doi.org/10.1007/978-3-642-27340-7_11openalex-snapshot
Liver Injury and Disease Pathogenesis in Chronic Hepatitis C
inferred← citeshttps://doi.org/10.1007/978-3-642-30018-9_198openalex-snapshot
Reactive Oxygen Species as Potential Mediators of Obesity-Related Cardiovascular Complications
inferred← citeshttps://doi.org/10.1007/978-3-642-30018-9_44openalex-snapshot
Dietary Fatty Acids, Redox Signaling, and the Heart
inferred← citeshttps://doi.org/10.1007/978-3-662-67753-7_7openalex-snapshot
Ausdauer: Mikrozirkulation, aerober Energiestoffwechsel, Sarkopenie, Schmerzen
inferred← citeshttps://doi.org/10.1007/978-88-470-2418-2_8openalex-snapshot
Muscle Biopsy To Investigate Mitochondrial Turnover
inferred← citeshttps://doi.org/10.1007/978-94-007-2869-1_5openalex-snapshot
Mitochondria and Reactive Oxygen Species. Which Role in Physiology and Pathology?
inferred← citeshttps://doi.org/10.1007/978-94-007-2869-1_9openalex-snapshot
Role of Mitochondrial Function in Insulin Resistance
inferred← citeshttps://doi.org/10.1007/978-981-13-8367-0_9openalex-snapshot
Investigating the Role of Mitochondria in Type 2 Diabetes – Lessons from Lipidomics and Proteomics Studies of Skeletal Muscle and Liver
inferred← citeshttps://doi.org/10.1007/s00018-019-03148-8openalex-snapshot
Proinflammatory NFkB signalling promotes mitochondrial dysfunction in skeletal muscle in response to cellular fuel overloading
inferred← citeshttps://doi.org/10.1007/s00018-023-04761-4openalex-snapshot
Chronic stress targets mitochondrial respiratory efficiency in the skeletal muscle of C57BL/6 mice
inferred← citeshttps://doi.org/10.1007/s00109-012-0887-yopenalex-snapshot
Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle
inferred← citeshttps://doi.org/10.1007/s00109-015-1278-yopenalex-snapshot
Mitoflash altered by metabolic stress in insulin-resistant skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00125-008-1122-9openalex-snapshot
Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genes
inferred← citeshttps://doi.org/10.1007/s00125-009-1354-3openalex-snapshot
Continuous low- to moderate-intensity exercise training is as effective as moderate- to high-intensity exercise training at lowering blood HbA1c in obese type 2 diabetes patients
inferred← citeshttps://doi.org/10.1007/s00125-010-1830-9openalex-snapshot
High-fat feeding stimulates endocrine, glucose-dependent insulinotropic polypeptide (GIP)-expressing cell hyperplasia in the duodenum of Wistar rats
inferred← citeshttps://doi.org/10.1007/s00125-010-2001-8openalex-snapshot
Oltipraz upregulates the nuclear respiratory factor 2 alpha subunit (NRF2) antioxidant system and prevents insulin resistance and obesity induced by a high-fat diet in C57BL/6J mice
inferred← citeshttps://doi.org/10.1007/s00125-011-2396-xopenalex-snapshot
Fatty acids acutely enhance insulin-induced oxidative stress and cause insulin resistance by increasing mitochondrial reactive oxygen species (ROS) generation and nuclear factor-κB inhibitor (IκB)–nuclear factor-κB (NFκB) activation in rat muscle, in the absence of mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1007/s00125-012-2626-xopenalex-snapshot
Targeting of mitochondrial reactive oxygen species production does not avert lipid-induced insulin resistance in muscle tissue from mice
inferred← citeshttps://doi.org/10.1007/s00125-022-05797-0openalex-snapshot
Hyperbaric oxygen rapidly improves tissue-specific insulin sensitivity and mitochondrial capacity in humans with type 2 diabetes: a randomised placebo-controlled crossover trial
inferred← citeshttps://doi.org/10.1007/s00280-016-3045-3openalex-snapshot
Mitochondria: Inadvertent targets in chemotherapy-induced skeletal muscle toxicity and wasting?
inferred← citeshttps://doi.org/10.1007/s00394-009-0019-9openalex-snapshot
Tachyphylaxis effects on postprandial oxidative stress and mitochondrial-related gene expression in overweight subjects after a period of energy restriction
inferred← citeshttps://doi.org/10.1007/s00394-015-1086-8openalex-snapshot
Effects of chronic sugar consumption on lipid accumulation and autophagy in the skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00394-017-1477-0openalex-snapshot
Oxidative damage of mitochondrial respiratory chain in different organs of a rat model of diet-induced obesity
inferred← citeshttps://doi.org/10.1007/s00394-024-03437-4openalex-snapshot
Association of ultra-processed food consumption with muscle mass among young and middle-aged US adults
inferred← citeshttps://doi.org/10.1007/s00395-013-0329-1openalex-snapshot
Impaired mitochondrial biogenesis due to dysfunctional adiponectin-AMPK-PGC-1α signaling contributing to increased vulnerability in diabetic heart
inferred← citeshttps://doi.org/10.1007/s00441-014-1900-2openalex-snapshot
Testosterone is essential for skeletal muscle growth in aged mice in a heterochronic parabiosis model
inferred← citeshttps://doi.org/10.1007/s00580-017-2479-2openalex-snapshot
The effects of Amygdalus scoparia extract on ultrastructure changes of photoreceptor layer in diabetic rats
inferred← citeshttps://doi.org/10.1007/s10068-015-0041-zopenalex-snapshot
Anti-hyperglycemic and hypolipidemic effects of baechukimchi with Ecklonia cava in type 2 diabetic db/db mice
inferred← citeshttps://doi.org/10.1007/s10142-013-0342-3openalex-snapshot
Mitochondrial-related proteomic changes during obesity and fasting in mice are greater in the liver than skeletal muscles
inferred← citeshttps://doi.org/10.1007/s10495-014-1021-0openalex-snapshot
ClC-3 deficiency protects preadipocytes against apoptosis induced by palmitate in vitro and in type 2 diabetes mice
inferred← citeshttps://doi.org/10.1007/s10495-015-1128-yopenalex-snapshot
Fructose induces mitochondrial dysfunction and triggers apoptosis in skeletal muscle cells by provoking oxidative stress
inferred← citeshttps://doi.org/10.1007/s10495-024-02069-7openalex-snapshot
Combined effects of natural products and exercise on apoptosis pathways in obesity-related skeletal muscle dysfunction
inferred← citeshttps://doi.org/10.1007/s10495-026-02315-0openalex-snapshot
Mitochondria-associated programmed cell death in pancreatic β cell of T2DM
inferred← citeshttps://doi.org/10.1007/s10545-009-1263-0openalex-snapshot
Mitochondria and diabetes mellitus: untangling a conflictive relationship?
inferred← citeshttps://doi.org/10.1007/s10735-023-10158-1openalex-snapshot
Mitochondria as a target for exercise-mitigated type 2 diabetes
inferred← citeshttps://doi.org/10.1007/s10863-012-9440-5openalex-snapshot
α-Lipoic acid protects 3T3-L1 adipocytes from NYGGF4 (PID1) overexpression-induced insulin resistance through increasing phosphorylation of IRS-1 and Akt
inferred← citeshttps://doi.org/10.1007/s10863-012-9460-1openalex-snapshot
α-Lipoic acid ameliorates impaired glucose uptake in LYRM1 overexpressing 3T3-L1 adipocytes through the IRS-1/Akt signaling pathway
inferred← citeshttps://doi.org/10.1007/s10863-012-9472-xopenalex-snapshot
NYGGF4 (PID1) effects on insulin resistance are reversed by metformin in 3T3-L1 adipocytes
inferred← citeshttps://doi.org/10.1007/s11010-010-0398-5openalex-snapshot
Overexpression of NYGGF4 (PID1) induces mitochondrial impairment in 3T3-L1 adipocytes
inferred← citeshttps://doi.org/10.1007/s11011-019-00443-yopenalex-snapshot
Allicin ameliorates obesity comorbid depressive-like behaviors: involvement of the oxidative stress, mitochondrial function, autophagy, insulin resistance and NOX/Nrf2 imbalance in mice
inferred← citeshttps://doi.org/10.1007/s11011-024-01350-7openalex-snapshot
Berberine attenuates brain aging via stabilizing redox homeostasis and inflammation in an accelerated senescence model of Wistar rats
inferred← citeshttps://doi.org/10.1007/s11033-018-4551-7openalex-snapshot
Cytosolic lipid excess-induced mitochondrial dysfunction is the cause or effect of high fat diet-induced skeletal muscle insulin resistance: a molecular insight
inferred← citeshttps://doi.org/10.1007/s11033-020-06081-3openalex-snapshot
Unfolding Nrf2 in diabetes mellitus
inferred← citeshttps://doi.org/10.1007/s11154-014-9305-9openalex-snapshot
The role of the Nrf2/Keap1 pathway in obesity and metabolic syndrome
inferred← citeshttps://doi.org/10.1007/s11325-025-03504-yopenalex-snapshot
PGC-1α: a potential therapeutic target for upper airway dilator muscle structure and dysfunction in OSA
inferred← citeshttps://doi.org/10.1007/s11356-016-6348-3openalex-snapshot
Polychlorinated biphenyl 126 exposure in L6 myotubes alters glucose metabolism: a pilot study
inferred← citeshttps://doi.org/10.1007/s11356-018-3738-8openalex-snapshot
Polychlorinated biphenyl 126 exposure in rats alters skeletal muscle mitochondrial function
inferred← citeshttps://doi.org/10.1007/s11357-009-9125-0openalex-snapshot
Absence of insulin signalling in skeletal muscle is associated with reduced muscle mass and function: evidence for decreased protein synthesis and not increased degradation
inferred← citeshttps://doi.org/10.1007/s11695-019-03800-zopenalex-snapshot
Gastric Bypass Surgery Improves the Skeletal Muscle Ceramide/S1P Ratio and Upregulates the AMPK/ SIRT1/ PGC-1α Pathway in Zucker Diabetic Fatty Rats
inferred← citeshttps://doi.org/10.1007/s11745-014-3964-xopenalex-snapshot
Alpha‐Lipoic Acid Supplementation Reduces mTORC1 Signaling in Skeletal Muscle from High Fat Fed, Obese Zucker Rats
inferred← citeshttps://doi.org/10.1007/s11883-012-0237-0openalex-snapshot
Mitochondrial Reactive Oxygen Species and Risk of Atherosclerosis
inferred← citeshttps://doi.org/10.1007/s11906-010-0157-8openalex-snapshot
Mitochondrial Biogenesis and Fragmentation as Regulators of Muscle Protein Degradation
inferred← citeshttps://doi.org/10.1007/s12013-012-9496-1openalex-snapshot
Overexpression of TFAM Protects 3T3-L1 Adipocytes from NYGGF4 (PID1) Overexpression-Induced Insulin Resistance and Mitochondrial Dysfunction
inferred← citeshttps://doi.org/10.1007/s12013-014-9971-yopenalex-snapshot
Knockdown of LYRM1 Rescues Insulin Resistance and Mitochondrial Dysfunction Induced by FCCP in 3T3-L1 Adipocytes
inferred← citeshttps://doi.org/10.1007/s12013-018-0860-7openalex-snapshot
The Effects of Resveratrol, Metformin, Cold and Strength Training on the Level of Perilipin 5 in the Heart, Skeletal Muscle and Brown Adipose Tissues in Mouse
inferred← citeshttps://doi.org/10.1007/s12020-009-9270-3openalex-snapshot
Variation in gene expression of presenilins-associated rhomboid-like protein and mitochondrial function in skeletal muscle of insulin-resistant rats
inferred← citeshttps://doi.org/10.1007/s12020-016-0976-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12035-026-06181-4openalex-snapshot
Tert-Butylhydroquinone Reversed Age-Dependent Hypothalamic Mitochondrial Dysfunction Linking Maternal Fructose Exposure to Synaptic Vulnerability
inferred← citeshttps://doi.org/10.1007/s12195-017-0488-5openalex-snapshot
Oxidative Stress Alters the Morphological Responses of Myoblasts to Single-Site Membrane Photoporation
inferred← citeshttps://doi.org/10.1007/s12576-018-0614-8openalex-snapshot
Effect of downhill walking on next-day muscle damage and glucose metabolism in healthy young subjects
inferred← citeshttps://doi.org/10.1007/s12576-019-00692-7openalex-snapshot
Effects of astaxanthin supplementation and electrical stimulation on muscle atrophy and decreased oxidative capacity in soleus muscle during hindlimb unloading in rats
inferred← citeshttps://doi.org/10.1007/s12603-011-0366-0openalex-snapshot
Discovering pathways of sarcopenia in older adults: A role for insulin resistance on mitochondria dysfunction
inferred← citeshttps://doi.org/10.1007/s13105-015-0392-1openalex-snapshot
Resveratrol improves high-fat diet induced insulin resistance by rebalancing subsarcolemmal mitochondrial oxidation and antioxidantion
inferred← citeshttps://doi.org/10.1007/s13277-015-3702-xopenalex-snapshot
Oxidative stress induced by low-dose doxorubicin promotes the invasiveness of osteosarcoma cell line U2OS in vitro
inferred← citeshttps://doi.org/10.1007/s13668-024-00555-7openalex-snapshot
Mitochondrial Adaptation in Skeletal Muscle: Impact of Obesity, Caloric Restriction, and Dietary Compounds
inferred← citeshttps://doi.org/10.1007/s13679-019-00360-2openalex-snapshot
The Role of Adipose Tissue and Adipokines in Sepsis: Inflammatory and Metabolic Considerations, and the Obesity Paradox
inferred← citeshttps://doi.org/10.1007/s13679-021-00434-0openalex-snapshot
The Role of Mitochondrial Adaptation and Metabolic Flexibility in the Pathophysiology of Obesity and Insulin Resistance: an Updated Overview
inferred← citeshttps://doi.org/10.1007/s40279-015-0394-8openalex-snapshot
The Physiological Regulation of Skeletal Muscle Fatty Acid Supply and Oxidation During Moderate-Intensity Exercise
inferred← citeshttps://doi.org/10.1007/s40279-016-0566-1openalex-snapshot
The Antioxidant Effect of Exercise: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.1007/s40519-018-0481-6openalex-snapshot
Insulin resistance in obesity: an overview of fundamental alterations
inferred← citeshttps://doi.org/10.1007/s40618-020-01381-8openalex-snapshot
Testosterone treatment is associated with reduced adipose tissue dysfunction and nonalcoholic fatty liver disease in obese hypogonadal men
inferred← citeshttps://doi.org/10.1016/b978-0-12-405881-1.00016-1openalex-snapshot
Effects of H2O2 on Insulin Signaling the Glucose Transport System in Mammalian Skeletal Muscle
inferred← citeshttps://doi.org/10.1016/b978-0-12-800101-1.00008-9openalex-snapshot
Free Fatty Acids and Skeletal Muscle Insulin Resistance
inferred← citeshttps://doi.org/10.1016/b978-0-12-809868-4.00013-3openalex-snapshot
Benefits of Lactobacillus helveticus Fermented Milk in Sports and Health
inferred← citeshttps://doi.org/10.1016/b978-0-12-810422-4.00009-9openalex-snapshot
Skeletal Muscle Mitochondrial, Obesity, and High-Fat Feeding
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00001-8openalex-snapshot
Mitochondria: Ultrastructure, Dynamics, Biogenesis and Main Functions
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00002-xopenalex-snapshot
Mitochondria as Signaling Platforms
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00006-7openalex-snapshot
Role of Mitochondria in the Skeletal Muscle Metabolism in Obesity and Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/b978-0-323-85732-1.00043-8openalex-snapshot
Mitochondrial dysfunction and metabolic syndrome
inferred← citeshttps://doi.org/10.1016/j.animal.2025.101551openalex-snapshot
Early high nutrition enhances grass-fed beef productivity through epigenetically regulated muscle metabolism, altered early adipogenesis, and rumen fermentation dynamics
inferred← citeshttps://doi.org/10.1016/j.appet.2015.03.003openalex-snapshot
Increased 24-hour ad libitum food intake is associated with lower plasma irisin concentrations the following morning in adult humans
inferred← citeshttps://doi.org/10.1016/j.apsb.2012.06.010openalex-snapshot
Mitochondrial inhibitor as a new class of insulin sensitizer
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2011.08.037openalex-snapshot
Association of mitochondrial function with feed efficiency in rainbow trout: Diets and family effects
inferred← citeshttps://doi.org/10.1016/j.arr.2023.102087openalex-snapshot
Exercise mitigates age-related metabolic diseases by improving mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1016/j.arres.2024.100100openalex-snapshot
The complex interplay between oxinflammation, mitochondrial dysfunction and lipotoxicity: Focus on their role in the pathogenesis of skeletal muscle insulin resistance and modulation by dietary fatty acids
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2015.04.805openalex-snapshot
Glutaredoxin 2a overexpression in macrophages promotes mitochondrial dysfunction but has little or no effect on atherogenesis in LDL-receptor null mice
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.01.025openalex-snapshot
Mitochondrial respiratory chain super-complex I–III in physiology and pathology
inferred← citeshttps://doi.org/10.1016/j.bbabio.2016.07.008openalex-snapshot
Mitochondrial involvement in skeletal muscle insulin resistance: A case of imbalanced bioenergetics
inferred← citeshttps://doi.org/10.1016/j.bbadis.2011.10.008openalex-snapshot
Berberine protects against high fat diet-induced dysfunction in muscle mitochondria by inducing SIRT1-dependent mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1016/j.bbadis.2012.04.009openalex-snapshot
Impaired protein quality control system underlies mitochondrial dysfunction in skeletal muscle of streptozotocin-induced diabetic rats
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.05.008openalex-snapshot
Increased proton leak and SOD2 expression in myotubes from obese non-diabetic subjects with a family history of type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.05.012openalex-snapshot
Synergistic effects of β-amyloid and ceramide-induced insulin resistance on mitochondrial metabolism in neuronal cells
inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165801openalex-snapshot
Interplay between NADH oxidation by complex I, glutathione redox state and sirtuin-3, and its role in the development of insulin resistance
inferred← citeshttps://doi.org/10.1016/j.bbagen.2013.09.019openalex-snapshot
The role of mitochondria in the aetiology of insulin resistance and type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.bbagen.2013.12.004openalex-snapshot
Mitochondrial function in metabolic health: A genetic and environmental tug of war
inferred← citeshttps://doi.org/10.1016/j.bbagen.2015.05.009openalex-snapshot
Role of crystallins in diabetic complications
inferred← citeshttps://doi.org/10.1016/j.bbalip.2009.09.011openalex-snapshot
Mitochondrial dysfunction and lipotoxicity
inferred← citeshttps://doi.org/10.1016/j.bbalip.2009.09.014openalex-snapshot
Role of fatty acid uptake and fatty acid β-oxidation in mediating insulin resistance in heart and skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.bbalip.2009.11.007openalex-snapshot
Intramuscular triacylglycerol and insulin resistance: Guilty as charged or wrongly accused?
inferred← citeshttps://doi.org/10.1016/j.bbalip.2017.05.011openalex-snapshot
Mitochondria and endoplasmic reticulum: Targets for a better insulin sensitivity in skeletal muscle?
inferred← citeshttps://doi.org/10.1016/j.bbalip.2021.159030openalex-snapshot
Loss and gain of function of Grp75 or mitofusin 2 distinctly alter cholesterol metabolism, but all promote triglyceride accumulation in hepatocytes
inferred← citeshttps://doi.org/10.1016/j.bbr.2020.112501openalex-snapshot
Effects of aging on the motor, cognitive and affective behaviors, neuroimmune responses and hippocampal gene expression
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.09.115openalex-snapshot
ATP synthesis is impaired in isolated mitochondria from myotubes established from type 2 diabetic subjects
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.11.135openalex-snapshot
Reduction of endoplasmic reticulum stress using chemical chaperones or Grp78 overexpression does not protect muscle cells from palmitate-induced insulin resistance
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.04.038openalex-snapshot
Strenuous exercise induces mitochondrial damage in skeletal muscle of old mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.09.171openalex-snapshot
Down regulation of Peroxiredoxin-3 in 3T3-L1 adipocytes leads to oxidation of Rictor in the mammalian-target of rapamycin complex 2 (mTORC2)
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.04.002openalex-snapshot
Fibroblast growth factor 19 alleviates palmitic acid-induced mitochondrial dysfunction and oxidative stress via the AMPK/PGC-1α pathway in skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150158openalex-snapshot
Interleukin 38 improves insulin resistance in hyperlipidemic skeletal muscle cells via PPARδ/SIRT1-mediated suppression of STAT3 signaling and oxidative stress
inferred← citeshttps://doi.org/10.1016/j.bcp.2015.06.032openalex-snapshot
Pharmacological induction of mitochondrial biogenesis as a therapeutic strategy for the treatment of type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.beem.2011.09.003openalex-snapshot
Metabolic insights from extreme human insulin resistance phenotypes
inferred← citeshttps://doi.org/10.1016/j.beem.2012.06.001openalex-snapshot
Skeletal muscle mitochondrial energetics in obesity and type 2 diabetes mellitus: Endocrine aspects
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.02.004openalex-snapshot
Role of mitochondrial dynamics proteins in the pathophysiology of obesity and type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.biocel.2011.05.006openalex-snapshot
Mitochondria and endoplasmic reticulum: Mitochondria–endoplasmic reticulum interplay in type 2 diabetes pathophysiology
inferred← citeshttps://doi.org/10.1016/j.biocel.2012.09.019openalex-snapshot
Insulin resistance and mitochondrial function in skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.biocel.2016.08.024openalex-snapshot
Proteomic profiling reveals oxidative phosphorylation pathway is suppressed in longissimus dorsi muscle of weaned piglets fed low-protein diet supplemented with limiting amino acids
inferred← citeshttps://doi.org/10.1016/j.biochi.2013.07.017openalex-snapshot
Ectopic lipid accumulation: A potential cause for metabolic disturbances and a contributor to the alteration of kidney function
inferred← citeshttps://doi.org/10.1016/j.biochi.2016.11.013openalex-snapshot
Targeted mitochondrial uncoupling beyond UCP1 – The fine line between death and metabolic health
inferred← citeshttps://doi.org/10.1016/j.ceca.2017.01.003openalex-snapshot
The endoplasmic reticulum-mitochondria coupling in health and disease: Molecules, functions and significance
inferred← citeshttps://doi.org/10.1016/j.cellsig.2016.06.024openalex-snapshot
Alpha-lipoic acid attenuates endoplasmic reticulum stress-induced insulin resistance by improving mitochondrial function in HepG2 cells
inferred← citeshttps://doi.org/10.1016/j.clnu.2011.05.009openalex-snapshot
Oleate-enriched diet improves insulin sensitivity and restores muscle protein synthesis in old rats
inferred← citeshttps://doi.org/10.1016/j.cmet.2008.04.005openalex-snapshot
IRS1-Independent Defects Define Major Nodes of Insulin Resistance
inferred← citeshttps://doi.org/10.1016/j.cmet.2010.07.003openalex-snapshot
Cardiolipin Remodeling by ALCAT1 Links Oxidative Stress and Mitochondrial Dysfunction to Obesity
inferred← citeshttps://doi.org/10.1016/j.cmet.2010.11.004openalex-snapshot
Targeted Expression of Catalase to Mitochondria Prevents Age-Associated Reductions in Mitochondrial Function and Insulin Resistance
inferred← citeshttps://doi.org/10.1016/j.cmet.2011.05.013openalex-snapshot
Cardiotrophin-1 Is a Key Regulator of Glucose and Lipid Metabolism
inferred← citeshttps://doi.org/10.1016/j.cmet.2012.04.010openalex-snapshot
Lipid-Induced Mitochondrial Stress and Insulin Action in Muscle
inferred← citeshttps://doi.org/10.1016/j.cmet.2013.03.002openalex-snapshot
Mitochondrial Dynamics in the Regulation of Nutrient Utilization and Energy Expenditure
inferred← citeshttps://doi.org/10.1016/j.cophys.2019.05.003openalex-snapshot
Redox regulation of metabolic syndrome: recent developments in skeletal muscle insulin resistance and non-alcoholic fatty liver disease (NAFLD)
inferred← citeshttps://doi.org/10.1016/j.diabet.2009.02.002openalex-snapshot
Is skeletal muscle mitochondrial dysfunction a cause or an indirect consequence of insulin resistance in humans?
inferred← citeshttps://doi.org/10.1016/j.diabet.2015.02.006openalex-snapshot
Contribution of mitochondria and endoplasmic reticulum dysfunction in insulin resistance: Distinct or interrelated roles?
inferred← citeshttps://doi.org/10.1016/j.eclnm.2011.02.002openalex-snapshot
Clinical Nutrition University: Muscle physiology and bioenergetics
inferred← citeshttps://doi.org/10.1016/j.ejphar.2014.06.008openalex-snapshot
Pioglitazone ameliorates the lowered exercise capacity and impaired mitochondrial function of the skeletal muscle in type 2 diabetic mice
inferred← citeshttps://doi.org/10.1016/j.ejphar.2014.10.049openalex-snapshot
Free fatty acid induced impairment of insulin signaling is prevented by the diastereomeric mixture of calophyllic acid and isocalophyllic acid in skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/j.ejphar.2015.05.017openalex-snapshot
Apelin receptors: From signaling to antidiabetic strategy
inferred← citeshttps://doi.org/10.1016/j.exger.2015.07.015openalex-snapshot
Blood-cell bioenergetics are associated with physical function and inflammation in overweight/obese older adults
inferred← citeshttps://doi.org/10.1016/j.exger.2024.112465openalex-snapshot
Aging-dependent mitochondrial bioenergetic impairment in the skeletal muscle of NNT-deficient mice
inferred← citeshttps://doi.org/10.1016/j.expneurol.2015.10.002openalex-snapshot
Thidoredxin-2 overexpression fails to rescue chronic high calorie diet induced hippocampal dysfunction
inferred← citeshttps://doi.org/10.1016/j.fct.2020.111477openalex-snapshot
Attenuation of arsenic induced high fat diet exacerbated oxidative stress mediated hepatic and cardiac injuries in male Wistar rats by piperine involved antioxidative mechanisms
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.11.012openalex-snapshot
Significance of uncoupling protein 3 in mitochondrial function upon mid- and long-term dietary high-fat exposure
inferred← citeshttps://doi.org/10.1016/j.foodchem.2015.03.038openalex-snapshot
Effects of long-term consumption of standard diets including glucose–lysine model glycated compounds on the antioxidant status of adult rats
inferred← citeshttps://doi.org/10.1016/j.foodres.2014.06.004openalex-snapshot
Antioxidant balance after long-term consumption of standard diets including bread crust glycated compounds by adult rats
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2008.11.020openalex-snapshot
Oxidative stress in rats fed a high-fat high-sucrose diet and preventive effect of polyphenols: Involvement of mitochondrial and NAD(P)H oxidase systems
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2009.12.006openalex-snapshot
Inhibition of SREBP-1c-mediated hepatic steatosis and oxidative stress by sauchinone, an AMPK-activating lignan in Saururus chinensis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.04.013openalex-snapshot
Gallic acid prevents nonsteroidal anti-inflammatory drug-induced gastropathy in rat by blocking oxidative stress and apoptosis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.09.001openalex-snapshot
Inhibition of liver X receptor-α-dependent hepatic steatosis by isoliquiritigenin, a licorice antioxidant flavonoid, as mediated by JNK1 inhibition
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.09.003openalex-snapshot
Mitochondrial decay is involved in BaP-induced cervical damage
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.12.006openalex-snapshot
Oxidative stress, insulin signaling, and diabetes
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2011.01.019openalex-snapshot
Mitochondrial complex I impairment in leukocytes from type 2 diabetic patients
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.03.015openalex-snapshot
Mitochondrial dysfunction accounts for aldosterone-induced epithelial-to-mesenchymal transition of renal proximal tubular epithelial cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.04.011openalex-snapshot
Obesity-induced tissue free radical generation: An in vivo immuno-spin trapping study
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.09.014openalex-snapshot
Redox regulation of mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.08.169openalex-snapshot
Redox-sensitive glycogen synthase kinase 3β-directed control of mitochondrial permeability transition: rheostatic regulation of acute kidney injury
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.09.014openalex-snapshot
Role of oxidative stress in impaired insulin signaling associated with exercise-induced muscle damage
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.09.019openalex-snapshot
Protein tyrosine phosphatase 1B inhibition ameliorates palmitate-induced mitochondrial dysfunction and apoptosis in skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.11.029openalex-snapshot
Hydroxytyrosol prevents diet-induced metabolic syndrome and attenuates mitochondrial abnormalities in obese mice
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.08.009openalex-snapshot
Cardiac mitochondrial biogenesis in endotoxemia is not accompanied by mitochondrial function recovery
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.07.154openalex-snapshot
NOD2 activation induces oxidative stress contributing to mitochondrial dysfunction and insulin resistance in skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.11.026openalex-snapshot
Diabetes-induced hepatic oxidative stress: a new pathogenic role for glycated albumin
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.10.012openalex-snapshot
Reactive oxygen species enhance mitochondrial function, insulin sensitivity and glucose uptake in skeletal muscle of senescence accelerated prone mice SAMP8
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.08.034openalex-snapshot
Mitochondrial calcium transport and the redox nature of the calcium-induced membrane permeability transition
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.10.422openalex-snapshot
Attenuation of oxidative stress-induced lesions in skeletal muscle in a mouse model of obesity-independent hyperlipidaemia and atherosclerosis through the inhibition of Nox2 activity
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.03.010openalex-snapshot
Double C-2 like domain beta (DOC2B) induces calcium dependent oxidative stress to promote lipotoxicity and mitochondrial dysfunction for its tumor suppressive function
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