Regulation of skeletal muscle fat oxidation during exercise in humans.

نویسنده

  • Lawrence L Spriet
چکیده

Fat and carbohydrate are the major energy substrates during aerobic exercise in well-fed humans. The regulation of fat metabolism during exercise has not been as thoroughly studied as carbohydrate metabolism, especially in human skeletal muscle. Traditionally, it was believed that the regulation of skeletal muscle fat metabolism was mainly at the level of the delivery of free fatty acids to the muscle (adipose tissue lipolysis) and transport of the long chain fatty acids into the mitochondria. It is now known that the transport of fatty acids into the muscle cell and the regulation of muscle triacylglycerol lipase activity are also important sites of regulation. New lines of research are currently underway examining the regulation of fat metabolism in skeletal muscle at the level of fat transport across the sarcolemmal and mitochondrial membranes and regulation of TG lipase activity in both rodent and human models. A major goal of this research is to determine the regulatory signals that control the up-regulation of fat metabolism during the transition from rest to low and moderate aerobic exercise (30-65% (.)VO(2max)) and the down-regulation that occurs when exercising at intense aerobic exercise (approximately 85% (.)VO(2max)). Although it is expected that the signals that activate carbohydrate metabolism during exercise (Ca and free ADP, AMP, and P(i)) would also play a role in fat metabolism, this has not been demonstrated to date.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Symposium: Limits to fat oxidation by skeletal muscle during exercise--introduction.

Lipids, in the form of adipose tissue triacylglycerol (TG), intramuscular triglyceride (IMTG), and dietary-derived fatty acids (FA) from plasma TG (chylomicrons), and very low-density lipoproteins (VLDL), represent the largest store of nutrient energy in humans. Yet despite the abundance of endogenous TG, there is limited capacity for FA oxidation during exercise: there are no mechanisms that m...

متن کامل

Skeletal muscle fat metabolism after exercise in humans: influence of fat availability.

The mechanisms facilitating increased skeletal muscle fat oxidation following prolonged, strenuous exercise remain poorly defined. The aim of this study was to examine the influence of plasma free fatty acid (FFA) availability on intramuscular malonyl-CoA concentration and the regulation of whole-body fat metabolism during a 6-h postexercise recovery period. Eight endurance-trained men performe...

متن کامل

Limits to Human Endurance: Carnitine and Fat Oxidation

Fat and carbohydrate are the primary fuel sources for mitochondrial ATP production in human skeletal muscle during endurance exercise. However, fat exhibits a relatively low maximal rate of oxidation in vivo, which begins to decline at around 65% of maximal oxygen consumption (VO2max) when muscle glycogen becomes the major fuel. It is thought that if the rate of fat oxidation during endurance e...

متن کامل

New Insights into the Interaction of Carbohydrate and Fat Metabolism During Exercise

Fat and carbohydrate are important fuels for aerobic exercise and there can be reciprocal shifts in the proportions of carbohydrate and fat that are oxidized. The interaction between carbohydrate and fatty acid oxidation is dependent on the intracellular and extracellular metabolic environments. The availability of substrate, both from inside and outside of the muscle, and exercise intensity an...

متن کامل

Transcriptional regulation of pyruvate dehydrogenase kinase 4 in skeletal muscle during and after exercise.

The pyruvate dehydrogenase complex (PDC) has a key position in skeletal muscle metabolism as it represents the entry of carbohydrate-derived fuel into the mitochondria for oxidation. PDC is regulated by a phosphorylation-dephosphorylation cycle, in which the pyruvate dehydrogenase kinase (PDK) phosphorylates and inactivates the complex. PDK exists in four isoforms, of which the PDK4 isoform is ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Medicine and science in sports and exercise

دوره 34 9  شماره 

صفحات  -

تاریخ انتشار 2002