Enhanced muscle fat oxidation and glucose transport by ACRP30 globular domain: Acetyl–CoA carboxylase inhibition and AMP-activated protein kinase activation
Boston University · Boston Medical Center · +2 more institutions
Abstract
GACRP30, the globular subunit of adipocyte complement-related protein of 30 kDa (ACRP30), improves insulin sensitivity and increases fatty acid oxidation. The mechanism by which gACRP30 exerts these effects is unknown. Here, we examined if gACRP30 activates AMP-activated protein kinase (AMPK), an enzyme that has been shown to increase muscle fatty acid oxidation and insulin sensitivity. Incubation of rat extensor digitorum longus (EDL), a predominantly fast twitch muscle, with gACRP30 (2.5 micro g/ml) for 30 min led to 2-fold increases in AMPK activity and phosphorylation of both AMPK on Thr-172 and acetyl CoA carboxylase (ACC) on Ser-79. Accordingly, concentration of malonyl CoA was diminished by 30%. In…
Citation impact
- FWCI
- 24.35
- Percentile
- 100%
- References
- 41
Authors
8- ETEva TomásCorresponding
Boston University, Boston Medical Center, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology
- TTTsu‐Shuen Tsao
Boston University, Boston Medical Center, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology
- AKAsish K. Saha
Boston University, Boston Medical Center, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology
- HEHeather E. Murrey
Boston University, Boston Medical Center, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology
- CZCheng Zhang
Boston University, Boston Medical Center, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology
Topics & keywords
- AMPK
- Acetyl-CoA carboxylase
- Protein kinase A
- AMP-activated protein kinase
- Beta oxidation
- Biochemistry
- Phosphorylation
- Chemistry