Defining body-weight reduction as a humane endpoint: a critical appraisal

Author:

Talbot Steven R1ORCID,Biernot Svenja1,Bleich Andre1ORCID,van Dijk Roelof Maarten2,Ernst Lisa3,Häger Christine1ORCID,Helgers Simeon Oscar Arnulfo4,Koegel Babette3,Koska Ines2,Kuhla Angela5,Miljanovic Nina2,Müller-Graff Franz-Tassilo5,Schwabe Kerstin4,Tolba Rene3ORCID,Vollmar Brigitte5,Weegh Nora1,Wölk Tjark5,Wolf Fabio2,Wree Andreas6,Zieglowski Leonie3,Potschka Heidrun2ORCID,Zechner Dietmar5ORCID

Affiliation:

1. Institute for Laboratory Animal Science, Hannover Medical School, Germany

2. Institute of Pharmacology, Toxicology, and Pharmacy, Ludwig-Maximilians-University, Germany

3. Institute for Laboratory Animal Science & Experimental Surgery and Central Laboratory for Laboratory Animal Science, RWTH Aachen University, Germany

4. Department of Neurosurgery, Hannover Medical School, Germany

5. Rudolf-Zenker-Institute of Experimental Surgery, University Medical Center, Rostock, Germany

6. Institute of Anatomy, University Medical Center, Rostock, Germany

Abstract

In many animal experiments scientists and local authorities define a body-weight reduction of 20% or more as severe suffering and thereby as a potential parameter for humane endpoint decisions. In this study, we evaluated distinct animal experiments in multiple research facilities, and assessed whether 20% body-weight reduction is a valid humane endpoint criterion in rodents. In most experiments (restraint stress, distinct models for epilepsy, pancreatic resection, liver resection, caloric restrictive feeding and a mouse model for Dravet syndrome) the animals lost less than 20% of their original body weight. In a glioma model, a fast deterioration in body weight of less than 20% was observed as a reliable predictor for clinical deterioration. In contrast, after induction of chronic diabetes or acute colitis some animals lost more than 20% of their body weight without exhibiting major signs of distress. In these two animal models an exclusive application of the 20% weight loss criterion for euthanasia might therefore result in an unnecessary loss of animals. However, we also confirmed that this criterion can be a valid parameter for defining the humane endpoint in other animal models, especially when it is combined with additional criteria for evaluating distress. In conclusion, our findings strongly suggest that experiment and model specific considerations are necessary for the rational integration of the parameter ‘weight loss’ in severity assessment schemes and humane endpoint criteria. A flexible implementation tailored to the experiment or intervention by scientists and authorities is therefore highly recommended.

Funder

Adhesys Medical GmbH

Bundesministerium für Bildung und Forschung

Deutsche Forschungsgemeinschaft

Publisher

SAGE Publications

Subject

General Veterinary,Animal Science and Zoology

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