Method Article

Measurement of Basal and Forskolin-stimulated Lipolysis in Inguinal Adipose Fat Pads

DOI:

10.3791/55625

July 21st, 2017

In This Article

Summary

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This protocol describes the method of determining basal and forskolin-stimulated lipolysis in inguinal fat pads obtained from normal chow diet (NCD) or high fat diet (HFD) ± capsaicin fed wild type mice. As an index for lipolysis, glycerol release was measured from inguinal adipose fat pads.

Abstract

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Lipolysis is a process by which the lipid stored as triglycerides in adipose tissues are hydrolyzed into glycerol and fatty acids. This article describes the method for the measurement of basal and forskolin (FSK)-stimulated lipolysis in the inguinal fat pads isolated from wild type mice fed either normal chow diet (NCD), high fat diet (HFD) or a high fat diet containing 0.01% of capsaicin (CAP; transient receptor potential vanilloid subfamily 1 (TRPV1) agonist) for 32 weeks. The method described here for performing ex vivo lipolysis is adopted from Schweiger et al.1 We present a detailed protocol for measuring glycerol levels by UV-Visible (UV/VIS) spectrophotometry. The method described here can be used to successfully isolate inguinal fat pads for lipolysis measurements to obtain consistent results. The protocol described for inguinal fat pads can readily be extended to measure lipolysis in other tissues.

Introduction

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Adipose tissues store energy as fat2 and fatty acid oxidation is required for thermogenesis3,4. Fatty acids ingested through diets are packaged along with apoproteins into chylomicrons and delivered to different tissues in the body via blood circulation. Although most cells in the body store a reserve of energy, adipose tissue stores excess energy as fat5,6. Lipolysis in adipose tissue is regulated by complex processes and the molecular details of lipolysis still remain vague7.

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Protocol

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All protocols follow the animal care guidelines of the University of Wyoming.

1. Animal Housing and Feeding

NOTE: Adult male wild type mice (C57BL/6) (age 12 to 24 weeks) were bred in the research animal facility as per the Institutional Animal Care and Use Committee (IACUC) approved protocols.

  1. Starting from week 6 of age, house mice in groups of four in separate cages and randomly assign them into feeding groups of NCD or HFD (± 0.01% CAP) until week 38 of age.
    NOTE: CAP is an agonist of TRPV1 channel protein expressed in adipose tissues11,

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Results

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To evaluate the effect of CAP on basal and stimulated lipolysis, this research measured lipolysis in inguinal adipose fat pads isolated from NCD or HFD (± CAP)-fed wild type mice. The representative results for the basal and FSK-stimulated lipolysis for the inguinal fat pads are given in Table I. Basal and FSK-stimulated glycerol release in the presence of Triacsin C, which inhibits acyl coA synthetase and prevents the regeneration of TGL. As shown in

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Discussion

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The breakdown process of TGL into glycerol and fatty acids is catalyzed by ATGL9 during basal lipolysis and orchestrated by an array of proteins including the activation of adenylyl cyclase/PKA-dependent pathway during stimulated lipolysis21,22,23. Enhancement of lipolysis increases the plasma levels of fatty acids for transportation and energy use24. Fatty acids are taken up by mi.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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This work was supported by the AHA Award No. 15BGIA23250030, the National Institute of General Medical Sciences of the NIH under award number 8P20 GM103432-12 and the University of Wyoming Faculty Grant in Aid to BT.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
CapsaicinSigma, USAM2028TRPV1 agonist
ForskolinSigma, USAF6886Adenylyl cyclase activator
DMEMGE healthcare and life sciences, UT, USASH30081.01
High fat dietResearch diets, New Brunswick, USAD12492Abbreviated as HFD
TrisAmresco, USAO497
Sodium chlorideThermofisher ScientificBP358-212
Sodium deoxycholateSigma, USAD6750
DithiothreitolSigma, USAD9163
Sodium orthovanadateSigma, USAS6508
Protease inhibitor cocktailSigma, USAP8340
Free Glycerol reagentSigma USAF6428
DMSOSigma, USAD8779
Triacsin CSigma, USAT4540Acyl CoA transferase inhibitor
Bovine serum albuminSigma, USAA7030
ChloroformSigma Aldrich31998-8
MethanolThermofisher Scientific, USAA412-1
Sodium hydroxideAmresco, USAO583
Sodium dodecyl sulfateSigma, USAL3371
Bicinchoninic acid reagentSigma, USABCA1-1KT
UV-VIS SpectrophotometerPharmacia Biotech, NJ, USAUltrospec 2000
Normal chow dietLabdiet.com500Iabreviated as NCD
C57BL/6 miceJackson Laboratory, CT, USAStock number000664wild type mice
ParafilmHeathrow Scientific, USAHS 234526A
Glycerol standardSigma, USAG7793

References

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  1. Schweiger, M., et al. Measurement of lipolysis. Methods Enzymol. 538, 171-193 (2014).
  2. Coelho, M., Oliveira, T., Fernandes, R. Biochemistry of adipose tissue: an endocrine organ. Arch Med Sci. 9 (2), 191-200 (2013).
  3. Richard, D., Picard, F.

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Tags

Lipolysis MeasurementInguinal Adipose TissueBasal LipolysisUV Visible SpectrophotometryGlycerol AssayFat Pad IsolationProtein ConcentrationAdipose BiologyTRPV1 Agonist

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