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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

In this protocol, methods relevant for BAT-optimized arteriovenous metabolomics using GC-MS in a mouse model are outlined. These methods allow for the acquisition of valuable insights into BAT-mediated metabolite exchange at the organismal level.

Abstract

Brown adipose tissue (BAT) plays a crucial role in regulating metabolic homeostasis through a unique energy expenditure process known as non-shivering thermogenesis. To achieve this, BAT utilizes a diverse menu of circulating nutrients to support its high metabolic demand. Additionally, BAT secretes metabolite-derived bioactive factors that can serve as either metabolic fuels or signaling molecules, facilitating BAT-mediated intratissue and/or intertissue communication. This suggests that BAT actively participates in systemic metabolite exchange, an interesting feature that is beginning to be explored. Here, we introduce a protocol for in vivo mouse-level optimized BAT arteriovenous metabolomics. The protocol focuses on relevant methods for thermogenic stimulations and an arteriovenous blood sampling technique using Sulzer's vein, which selectively drains interscapular BAT-derived venous blood and systemic arterial blood. Next, a gas chromatography-based metabolomics protocol using those blood samples is demonstrated. The use of this technique should expand the understanding of BAT-regulated metabolite exchange at the inter-organ level by measuring the net uptake and release of metabolites by BAT.

Introduction

Brown adipose tissue (BAT) possesses a unique energy expenditure property known as non-shivering thermogenesis (NST), which involves both mitochondrial uncoupling protein 1 (UCP1)-dependent and UCP1-independent mechanisms1,2,3,4,5. These distinctive characteristics implicate BAT in the regulation of systemic metabolism and the pathogenesis of metabolic diseases, including obesity, type 2 diabetes, cardiovascular disease, and cancer cachexia6,

Protocol

All experiments were conducted with the approval of the Sungkyunkwan University Institutional Animal Care and Use Committee (IACUC). Mice were housed in an IACUC-approved animal facility located in a clean room set at 22 °C and 45% humidity, following a daily 12 h light/dark cycle. They were kept in ventilated racks and had access to a standard chow diet ad libitum (comprising 60% carbohydrate, 16% protein, and 3% fat). Bedding and nesting materials were changed on a weekly basis. For this study, male C57BL/6J mice .......

Representative Results

Figure 1 illustrates the experimental scheme of BAT-optimized AV metabolomics. As mentioned in the Protocol section, to obtain differentially stimulated brown adipose tissues, mice undergo temperature acclimation using rodent incubators or receive pharmacological administration such as β-adrenergic receptor agonists. Subsequently, mice are anesthetized, and blood samples are collected for metabolomic analysis (Figure 1A). For blood sampling, venous blood sp.......

Discussion

A critical step in understanding the metabolic potential of BAT in whole-body energy balance is to define which nutrients it consumes, how they are metabolically processed, and what metabolites are released into the circulation. This protocol introduces a specialized arteriovenous sampling technique that enables access to the venous vasculature of interscapular BAT and systemic arterial vasculature in C57BL/6J mice, which was recently developed and validated by Park et al42. Below are key points y.......

Acknowledgements

We thank all members of the Choi and Jung laboratories for methodological discussion. We thank C. Jang and D. Guertin for advice and feedback. We thank M.S. Choi for critical reading of the manuscript. This work was funded by NRF-2022R1C1C1012034 to S.M.J.; NRF-2022R1C1C1007023 to D.W.C; NRF-2022R1A4A3024551 to S.M.J. and D.W.C. This work was supported by Chungnam National University for W.T.K. Figure 1 and Figure 2 were created using BioRender (http://biorender.com/).

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Materials

NameCompanyCatalog NumberComments
0.5-20 µL Filter TipsAxygenAX.TF-20-R-S
1 mL Syringe with attached needle - 26 G 5/8"BD Biosciences309597
Agilent 5977B GC/MSD (mass selective detector)AgilentG7077B
Agilent 7693A AutosamplerAgilentG4513A
Agilent 8890 GC SystemAgilentG3542A
Agilent J&W GC column (Capilary column) HP-5MS UIAgilent19091S-433UI
Agilent MassHunter Workstation software_MS Quantitative analysis(Quant-My-way)AgilentG3335-90240
C57BL/6J mouseDBLC57BL/6JBomTac
CentriVap -50 °C Cold Trap (with Stainless steel Lid)LABCONCO 7811041
DL-NorvalineSigma-AldrichN7502-25G
Eppendorf centrifuge 5430REppendorf5428000210
Eppendorf Safe-Lock Tubes 1.5 mLEppendorf30120086
Glass insert 250 μL Agilent5181-1270
Methanol (LC-MS grade)Sigma-AldrichQ34966-1L
Methoxyamine hydrochlorideSigma-Aldrich226904-5G
Microvette 200 Serum, 200 µL, cap red, flat baseSarstedt20.1290.100
MTBSTFASigma-Aldrich394882-100ML
Pyridine(anhydrous, 99.8%)Sigma-Aldrich270970-100ML
Refrigerated CentriVap Complete Vaccum ConcentratorsLABCONCO 7310041
Rodent dietSAFESAFE R+40-10
Rodent incubatorPower scientificRIT33SD
Ultra-Fine Pen Needles - 29 G 1/2"BD Biosciences328203
Vial Cap 9 mmAgilent5190-9067
Vial, ambr scrw wrtn 2 mLAgilent5190-9063
Vial, ambr scrw wrtn 2 mL+A2:C40AxygenPCR-02-C

References

  1. Cannon, B., Nedergaard, J. Brown adipose tissue: function and physiological significance. Physiol Rev. 84 (1), 277-359 (2004).
  2. Ikeda, K., et al. UCP1-inde....

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Arteriovenous MetabolomicsBrown Adipose TissueMetabolite ExchangeEnergy ExpenditureThermogenesisMouse ModelGas Chromatography based Metabolomics

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