Abstract

Increased lipid metabolism in muscle is associated with insulin resistance and therefore, many strategies have been employed to alter fatty acid metabolism and study the impact on insulin action. Metabolism of fatty acid requires activation to fatty acyl CoA by Acyl CoA synthases (ACSL) and fatty acyl CoA can be hydrolysed by Acyl CoA thioesterases (Acot). Thioesterase activity is low in muscle, so we overexpressed Acot7 in muscle of chow and high-fat diet (HFD) rats and investigated effects on insulin action. Acot7 overexpression modified specific phosphatidylcholine and phosphatidylethanolamine species in tibialis muscle of chow rats to levels similar to those observed in control HFD muscle. The changes in phospholipid species did not alter glucose uptake in tibialis muscle under hyperinsulinaemic/euglycaemic clamped conditions. Acot7 overexpression in white extensor digitorum longus (EDL) muscle increased complete fatty acid oxidation ex-vivo but was not associated with any changes in glucose uptake in-vivo, however overexpression of Acot7 in red EDL reduced insulin-stimulated glucose uptake in-vivo which correlated with increased incomplete fatty acid oxidation ex-vivo. In summary, although overexpression of Acot7 in muscle altered some aspects of lipid profile and metabolism in muscle, this had no major effect on insulin-stimulated glucose uptake.

Highlights

  • Insulin resistance and lipid accumulation in skeletal muscle are major risk factors for the development of Type 2 Diabetes[1]

  • Overexpression of Acyl CoA thioesterases (Acot)[7] might be expected to cleave the CoA group from fatty acids and alter the lipid profile in the muscle, an effect that could be limited if there was a compensatory increase in the opposing enzyme ACSL

  • Excess lipids from a high fat diet can lead to accumulation of various lipid species thought to impair insulin action in skeletal muscle[30]

Read more

Summary

Introduction

Insulin resistance and lipid accumulation in skeletal muscle are major risk factors for the development of Type 2 Diabetes[1]. Through either gain or loss of function studies, different Acots have been suggested to play important roles in triglyceride storage[11,12], fatty acid oxidation[11,12,13,14,15,16], mitochondrial function[15,16,17], energy expenditure[12,14], insulin signalling[17,18] and even lipid synthesis[14] in brown adipose, liver and heart tissues Changes in these pathways are reported to occur in skeletal muscle of HFD fed animals and have been speculated to either contribute to insulin resistance[19,20], or alleviate it[21,22,23,24]. The aim of this study was to use overexpression of cytoplasmic Acot7a25,26 to increase total muscle thioesterase activity and examine the effects on lipid composition and insulin-stimulated glucose uptake in skeletal muscle from chow and HFD fed animals

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call