Skeletal muscle malonyl-CoA content at the onset of exercise at varying power outputs in humans.

نویسندگان

  • L Maureen Odland
  • Richard A Howlett
  • George J F Heigenhauser
  • Eric Hultman
  • Lawrence L Spriet
چکیده

To investigate the regulation of intramuscular fuel selection, we measured the malonyl-CoA (M-CoA) content in human skeletal muscle at three exercise power outputs [35, 65, and 90% maximal rate of O2 consumption (V˙o 2 max)]. Four males and four females cycled for 10 min at one power output on three separate occasions with muscle biopsies sampled at rest and at 1 and 10 min. The respiratory exchange ratio was 0.84 ± 0.03, 0.92 ± 0.02, and >1.0 at 35, 65 and 90%V˙o 2 max, respectively. Muscle lactate content increased and phosphocreatine content decreased as a function of power output. Pyruvate dehydrogenase a activity increased from 0.40-0.64 mmol ⋅ kg wet muscle-1 ⋅ min-1at rest to 1.57 ± 0.28, 2.80 ± 0.41, and 3.28 ± 0.27 mmol ⋅ kg wet muscle-1 ⋅ min-1after 1 min of cycling at the three power outputs, respectively. Mean resting M-CoA contents were similar at all power outputs (1.85-1.98 μmol/kg dry muscle). During exercise at 35%V˙o 2 max, M-CoA decreased from rest at 1 min (1.85 ± 0.29 to 1.20 ± 0.12 μmol/kg dry muscle) but returned to rest level by 10 min (1.86 ± 0.25 μmol/kg dry muscle). M-CoA content did not decrease during cycling at 65%V˙o 2 max. At 90%V˙o 2 max, M-CoA did not increase despite significant acetyl-CoA accumulation (the substrate for M-CoA synthesis). The data suggest that a decrease in M-CoA content is not required for the increase in free fatty acid uptake and oxidation that occurs during exercise at 35 and 65%V˙o 2 max. Furthermore, M-CoA content does not increase during exercise at 90%V˙o 2 max and does not contribute to the lower rate of fat oxidation at this power output.

برای دانلود 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

Endurance training attenuates the decrease in skeletal muscle malonyl-CoA with exercise.

Muscle malonyl-CoA has been postulated to regulate fatty acid metabolism by inhibiting carnitine palmitoyltransferase 1. In nontrained rats, malonyl-CoA decreases in working muscle during exercise. Endurance training is known to increase a muscle's reliance on fatty acids as a substrate. This study was designed to investigate whether the decline in malonyl-CoA with exercise would be greater in ...

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

Malonyl-CoA and carnitine in regulation of fat oxidation in human skeletal muscle during exercise.

Intracellular mechanisms regulating fat oxidation were investigated in human skeletal muscle during exercise. Eight young, healthy, moderately trained men performed bicycle exercise (60 min, 65% peak O2 consumption) on two occasions, where they ingested either 1) a high-carbohydrate diet (H-CHO) or 2) a low-carbohydrate diet (L-CHO) before exercise to alter muscle glycogen content as well as to...

متن کامل

Increased malonyl-CoA and diacylglycerol content and reduced AMPK activity accompany insulin resistance induced by glucose infusion in muscle and liver of rats.

Glucose infusion in rats for 1-4 days results in insulin resistance and increased triglyceride, whole tissue long-chain fatty acyl-CoA (LCA-CoA), and malonyl-CoA content in red skeletal muscle. Despite this, the relation between these alterations and the onset of insulin resistance has not been defined. We aimed to 1) identify whether the changes in these lipids and of diacylglycerol (DAG) prec...

متن کامل

Insulin Resistance: Molecular Mechanism

Insulin resistance in skeletal muscle is present in humans with type 2 diabetes (non-insulin dependent diabetes mellitus) and obesity and in rodents with these disorders. Malonyl CoA is a regulator of carnitine palmitoyl transferase l (CAP I), the enzyme that controls the transfer of long chain fatty acyl CoA into mitochondria, where it is oxidized. In rat skeletal muscle, the formation of malo...

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

برای دانلود 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

عنوان ژورنال:
  • The American journal of physiology

دوره 274 6 Pt 1  شماره 

صفحات  -

تاریخ انتشار 1998