Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Short Communication
  • Published:

Reduced adipose tissue lymphatic drainage of macromolecules in obese subjects: a possible link between obesity and local tissue inflammation?

Abstract

The aim of this study was to investigate subcutaneous adipose tissue lymphatic drainage (ATLD) of macromolecules in lean and obese subjects and, furthermore, to evaluate whether ATLD may change in parallel with adipose tissue blood flow. Lean and obese male subjects were studied before and after an oral glucose load. Adipose-tissue blood flow was measured in the anterior subcutaneous abdominal adipose tissue by the 133Xe-washout technique. ATLD was measured as the disappearance rate of 99mTc-labelled nanoaggregated human albumin, during fasting and after an oral glucose load. A significant increase in ATLD was seen after the glucose load in the lean subjects. In the obese subjects, ATLD remained constant throughout the study and was significantly lower compared to the lean subjects. These results indicate a reduced ability to remove macromolecules from the interstitial space through the lymphatic system in obese subjects. Furthermore, they suggest that postprandial changes in ATLD taking place in lean subjects are not observed in obese subjects. This may have a role in the development of obesity-related inflammation in hypertrophic adipose tissue.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2

Similar content being viewed by others

References

  1. Ouchi N, Parker JL, Lugus JJ, Walsh K . Adipokines in inflammation and metabolic disease. Nat Rev Immunol 2011; 11: 85–97.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Dalmas E, Clément K, Guerre-Millo M . Defining macrophage phenotype and function in adipose tissue. Trends Immunol 2011; 32: 307–314.

    Article  CAS  PubMed  Google Scholar 

  3. Mohamed-Ali V, Goodrick S, Rawesh A, Katz DR, Miles JM, Yudkin JS et al. Subcutaneous adipose tissue releases interleukin-6, but not tumor necrosis factor-α, in vivo. J Clin Endocrinol Metab 1997; 82: 4196–4200.

    CAS  PubMed  Google Scholar 

  4. Clausen TS, Kaastrup P, Stallknecht B . Proinflammatory tissue response and recovery of adipokines during 4 days of subcutaneous large-pore microdialysis. J Pharmacol Toxicol Methods 2009; 60: 281–287.

    Article  CAS  PubMed  Google Scholar 

  5. Miller NE, Michel CC, Nanjee MN, Olszewski WL, Miller IP, Hazell M et al. Secretion of adipokines by human adipose tissue in vivo: partitioning between capillary and lymphatic transport. Am J Physiol Endocrinol Metab 2011; 301: 659–667.

    Article  Google Scholar 

  6. Summers LKM, Samra JS, Humphreys SM, Morris RJ, Frayn KN . Subcutaneous abdominal adipose tissue blood flow: variation within and between subjects and relationship to obesity. Clin Sci 1996; 91: 679–683.

    Article  CAS  Google Scholar 

  7. Tobin L, Simonsen L, Bülow J . Real-time contrast-enhanced ultrasound determination of microvascular blood volume in abdominal subcutaneous adipose tissue in man. Evidence for adipose tissue capillary recruitment. Clin Physiol Funct Imaging 2010; 30: 447–452.

    Article  CAS  PubMed  Google Scholar 

  8. Jensen MR, Simonsen L, Karlsmark T, Bülow J . Lymphoedema of the lower extremities -background, pathophysiology and diagnostic considerations. Clin Physiol Funct Imaging 2010; 30: 389–398.

    Article  PubMed  Google Scholar 

  9. Simonsen L, Enevoldsen LH, Bülow J . Determination of adipose tissue blood flow with local 133Xe clearance. Evaluation of a new labelling technique. Clin Physiol Funct Imaging 2003; 23: 320–323.

    Article  PubMed  Google Scholar 

  10. Bülow J, Jelnes R, Astrup A, Madsen J, Vilmann P . Tissue/blood partition coefficients for xenon in various adipose tissue depots in man. Scand J Clin Lab Invest 1987; 47: 1–3.

    Article  PubMed  Google Scholar 

  11. Spencer M, Unal R, Zhu B, Rasouli N, McGehee RE, Peterson CA et al. Adipose tissue extracellular matrix and vascular abnormalities in obesity and insulin resistance. J Clin Endocrinol Metab 2011; 96: 1990–1998.

    Article  Google Scholar 

  12. Divoux A, Clément K . Architecture and the extracellular matrix: the still unappreciated components of the adipose tissue. Obes Rev 2011; 12: 494–503.

    Article  Google Scholar 

  13. Uzarski J, Drelles MB, Gibbs SE, Ongstad EL, Goral JC, McKeown KK et al. The resolution of lymphedema by interstitial flow in the mouse tail skin. Am J Physiol Heart Circ Physiol 2008; 294: 1326–1334.

    Article  Google Scholar 

  14. Tobin L, Simonsen L, Bülow J . The dynamics of the microcirculation in the subcutaneous adipose tissue is impaired in the postprandial state in type 2 diabetes. Clin Physiol Funct Imaging 2011; 31: 458–463.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This study received financial support from the Novo Nordic Foundation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to N Arngrim.

Ethics declarations

Competing interests

The authors declare no conflict of interest.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Arngrim, N., Simonsen, L., Holst, J. et al. Reduced adipose tissue lymphatic drainage of macromolecules in obese subjects: a possible link between obesity and local tissue inflammation?. Int J Obes 37, 748–750 (2013). https://doi.org/10.1038/ijo.2012.98

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/ijo.2012.98

Keywords

This article is cited by

Search

Quick links