نتایج جستجو برای: Pyruvate Dehydrogenase Kinase 4 Endurance Training Metabolic Flexibility Estrogen

تعداد نتایج: 2123275  

Beydolah Shahouzehi, Hamid Marefati Saeed Shakerian, Soheil Aminizadeh, Yaser Masoumi-Ardakani

Background:Metabolic flexibility is the capacity of a system to adjust fuel (primarily glucose and fatty acids) oxidation based on nutrient availability. Pyruvate Dehydrogenase Kinase 4 (PDK4) is one of the main enzymes that play a critical role in metabolic flexibility. In current study, we examined PDK4 inhibition along with exercise training (ET) on the gene expression of Es...

Background and Objective: Maintaining a balance between energy demand and supply is critical for health. In this process, pyruvate dehydrogenase kinase 4 (PDK4) enzyme plays an important role to maintain energy homeostasis. So, the aim of the present study was to investigate the role of PDK4 on the expression of citrate synthase in the skeletal muscle after 4 weeks of endurance training in male...

Journal: :Journal of Oleo Science 2021

Endurance exercise training enhances muscle fat oxidation while concomitantly reducing carbohydrate (glycogen) utilization during exercise, thereby delaying the onset of fatigue. This study examined effects dietary restriction on endurance training-induced metabolic adaptations in rat skeletal muscle. Male Sprague-Dawley rats were placed either a control diet (CON: 19.2% protein, 21.6% fat, and...

2013
Clair Crewe Michael Kinter Luke I. Szweda

Cardiac function depends on the ability to switch between fatty acid and glucose oxidation for energy production in response to changes in substrate availability and energetic stress. In obese and diabetic individuals, increased reliance on fatty acids and reduced metabolic flexibility are thought to contribute to the development of cardiovascular disease. Mechanisms by which cardiac mitochondr...

2011
Helen J. Atherton Michael S. Dodd Julian L. Griffin Damian J. Tyler

Background—Hyperthyroidism increases heart rate, contractility, cardiac output, and metabolic rate. It is also accompanied by alterations in the regulation of cardiac substrate use. Specifically, hyperthyroidism increases the ex vivo activity of pyruvate dehydrogenase kinase, thereby inhibiting glucose oxidation via pyruvate dehydrogenase. Cardiac hypertrophy is another effect of hyperthyroidis...

Journal: :Circulation 2011
Helen J Atherton Michael S Dodd Lisa C Heather Marie A Schroeder Julian L Griffin George K Radda Kieran Clarke Damian J Tyler

BACKGROUND Hyperthyroidism increases heart rate, contractility, cardiac output, and metabolic rate. It is also accompanied by alterations in the regulation of cardiac substrate use. Specifically, hyperthyroidism increases the ex vivo activity of pyruvate dehydrogenase kinase, thereby inhibiting glucose oxidation via pyruvate dehydrogenase. Cardiac hypertrophy is another effect of hyperthyroidis...

Journal: :Livers 2021

Pyruvate metabolism is critical for all mammalian cells. The pyruvate dehydrogenase complex couples the formed as primary product of glycolysis to formation acetyl-CoA required substrate citric acid cycle. Dysregulation this coupling contributes alterations in metabolic flexibility obesity, diabetes, cancer, and more. kinase family isozymes phosphorylate inactive mitochondria. This function mak...

Journal: :Stroke 2015
Xiaokun Geng Omar Elmadhoun Changya Peng Xunming Ji Adam Hafeez Zongjian Liu Huishan Du Jose A Rafols Yuchuan Ding

BACKGROUND AND PURPOSE Ischemic stroke induces metabolic disarray. A central regulatory site, pyruvate dehydrogeanse complex (PDHC) sits at the cross-roads of 2 fundamental metabolic pathways: aerobic and anaerobic. In this study, we combined ethanol (EtOH) and normobaric oxygen (NBO) to develop a novel treatment to modulate PDHC and its regulatory proteins, namely pyruvate dehydrogenase phosph...

Journal: :Diabetes 2008
Thomas Cadoudal Emilie Distel Sylvie Durant Françoise Fouque Jean-Marc Blouin Martine Collinet Sylvie Bortoli Claude Forest Chantal Benelli

OBJECTIVE Pyruvate dehydrogenase complex (PDC) serves as the metabolic switch between glucose and fatty acid utilization. PDC activity is inhibited by PDC kinase (PDK). PDC shares the same substrate, i.e., pyruvate, as glyceroneogenesis, a pathway controlling fatty acid release from white adipose tissue (WAT). Thiazolidinediones activate glyceroneogenesis. We studied the regulation by rosiglita...

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