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In This Article

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

Summary

This animal model enables researchers to induce statistically significant secondary lymphedema in the hindlimb of mice, lasting at least 8 weeks. The model can be used to study the pathophysiology of lymphedema and to investigate novel treatment options.

Abstract

Animal models are of paramount importance in the research of lymphedema in order to understand the pathophysiology of the disease but also to explore potential treatment options. This mouse model allows researchers to induce significant lymphedema lasting at least 8 weeks. Lymphedema is induced using a combination of fractioned radiotherapy and surgical ablation of lymphatics. This model requires that the mice get a dose of 10 Gray (Gy) radiation before and after surgery. The surgical part of the model involves ligation of three lymph vessels and extraction of two lymph nodes from the mouse hindlimb. Having access to microsurgical tools and a microscope is essential, due to the small anatomical structures of mice. The advantage of this model is that it results in statistically significant lymphedema, which provides a good basis for evaluating different treatment options. It is also a great and easily available option for microsurgical training. The limitation of this model is that the procedure can be time consuming, especially if not practiced in advance. The model results in objectively quantifiable lymphedema in mice, without causing severe morbidity and has been tested in three separate projects.

Introduction

Lymphedema is characterized by an accumulation of lymph fluid that leads to localized tissue swelling, which mainly occurs due to impaired or disrupted flow of lymph fluid in the lymphatic vessels1. The lymph flow can be impaired or disrupted by infection, obstruction, injury or congenital defects in the lymphatic system2. These etiologies result in accumulation of lymphatic fluid, which leads to a chronic state of inflammation, resulting in subsequent fibrosis, as well as deposition of adipose tissue3. Lymphedema can be categorized as primary or secondary lymphedema. Primary lymphedema is caused ....

Protocol

Animals were housed in the University of Southern Denmark Animal Care Facility as per institutional guidelines. All procedures involving animal subjects have been approved by The Animal Experiments Inspectorate, Ministry of Environment and Food of Denmark.

1. Pre-surgery irradiation

NOTE: Pre-surgery irradiation takes place 7 days before surgery.

  1. Induce anesthesia.
    1. Place the mouse in an induction box and set the vaporizer to 3% isoflurane with an oxygen flow rate of 0.8−1.2 L/min to induce inhalation anesthesia.
      NOTE: Alternatively, injectable anesthetics can be used but for ....

Results

This procedure has previously been used in three separate experiments. All the experiments were made by different lead investigators who all are co-authors of this article. In all three experiments, great care was taken to adhere to the same procedure as described in this protocol. In all three experiments, secondary lymphedema was induced in one hindlimb while the other hindlimb served as a control. Volumes of the hindlimbs were the primary outcome in all three experiments.

Discussion

There are a few critical steps in this protocol. Firstly, it is important that the researchers take safety precautions when working with radioactivity. Secondly, during the surgical part of this protocol, it is important to start the procedure once the mouse has been anesthetized and finish it without unnecessary breaks. This is important to avoid an excessively long surgical period for the animal and to prevent that the anesthesia loses effect during surgery. It is recommended to only administer one bolus injection of a.......

Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors thank Peter Bollen, head of the Biomedical Laboratory for lending the equipment needed to record the footage seen through the microscopes.

....

Materials

NameCompanyCatalog NumberComments
10-0 Nylon sutureS&T12051-10
6-0 Nylon suture - DafilonB BraunC0933112
Coagulator - ICC 50ERBE
Cotton tipped applicatorsYibon medical co
Dissecting forcepsLawton09-0190
Elastic retractorsOdense University Hospital
Electrical clipperAesculapGT420
Fentanyl 0,315 mg/mlMatrix
Heating pad - PhysioSuiteKent Scientific Corp.
Isoflurane 1000mg AttaneScan Vet
Isoflurane vaporizer - PPVPenlon
Micro jewler forcepsLawton1405-05
Micro Needle holderLawton25679-14
Micro scissorsLawton10128-15
Micro tying forcepsLawton43953-10
Microfine U-40 syringe 0,5mlBD328821
Microlance syringe 25gBD
Microlance syringe 27gBD
Midazolam 5 mg/ml (hameln)Matrix
Needle holder - Circle woodLawton08-0065
Non woven swabsSelefa
Opmi pico microscope F170Zeiss
Patent blue V - 25 mg/mlGuerbet
Scissors - JosephBDRH1630
Siemens INVEON multimodality pre-clinical scannerSiemens pre-clinical solutions
Source of radiation - D3100Gulmay
Stata Statistical Software: Release 15StataCorp LLC
Temgesic - 0,2 mgIndivior
Vet eye ointment - viscotearsBausch & Lomb

References

  1. Lawenda, B. D., Mondry, T. E., Johnstone, P. A. S. Lymphedema: a primer on the identification and management of a chronic condition in oncologic treatment. CA: A Cancer Journal for Clinicians. 59 (1), 8-24 (2009).
  2. Greene, A. K., Greene, A. K., Slavin, S. A., Brorson, H.

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