Not all mice are equal: welfare implications of behavioural habituation profiles in four 129 mouse substrains.

PLoS One

Faculty of Veterinary Medicine, Department of Animals in Science and Society, Division of Animal Welfare and Laboratory Animal Science, Utrecht University, Utrecht, The Netherlands.

Published: January 2013

Safeguarding the welfare of animals is an important aim when defining housing and management standards in animal based, experimental research. While such standards are usually defined per animal species, it is known that considerable differences between laboratory mouse strains exist, for example with regard to their emotional traits. Following earlier experiments, in which we found that 129P3 mice show a lack of habituation of anxiety related behaviour after repeated exposure to an initially novel environment (non-adaptive profile), we here investigated four other 129 inbred mouse substrains (129S2/SvPas, 129S2/SvHsd (exp 1); 129P2 and 129X1 (exp 2)) on habituation of anxiety related behaviour. Male mice of each strain were repeatedly placed in the modified hole board test, measuring anxiety-related behaviour, exploratory and locomotor behaviour. The results reveal that all four substrains show a lack of habituation behaviour throughout the period of testing. Although not in all of the substrains a possible confounding effect of general activity can be excluded, our findings suggest that the genetic background of the 129 substrains may increase their vulnerability to cope with environmental challenges, such as exposure to novelty. This vulnerability might negatively affect the welfare of these mice under standard laboratory conditions when compared with other strains. Based on our findings we suggest to consider (sub)strain-specific guidelines and protocols, taking the (subs)train-specific adaptive capabilities into account.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411796PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0042544PLOS

Publication Analysis

Top Keywords

mouse substrains
8
lack habituation
8
habituation anxiety
8
anxiety behaviour
8
substrains
5
behaviour
5
mice
4
mice equal
4
equal welfare
4
welfare implications
4

Similar Publications

Aging is a complex biological process. Several animal models, including nematodes, Drosophila, and rodents, have been used in research on aging mechanisms and the extension of healthy life expectancy. The present study investigated the physiological and anatomical changes associated with aging in two sub-strains of aged C57BL/6 mice used in aging research: C57Bl/6NCrSlc (B6N) and C57BL/6J (B6J).

View Article and Find Full Text PDF

Objective: Recently, we revealed that triggering receptor expressed on myeloid cells-like 2 (TREML2) modulated inflammation by regulating microglial polarization and NLRP3 inflammasome activation. However, the role of TREML2 in Alzheimer's disease (AD) pathogenesis remains poorly understood. In this study, we tried to observe the impact of TREML2 on neuropathological hallmarks (including amyloid-β (Aβ) pathology, hyperphosphorylated tau and neuroinflammation) and cognitive deficiency in senescence-accelerated mouse prone substrain 8 (SAMP8) mice, an animal model of sporadic AD.

View Article and Find Full Text PDF

Concomitant with the opioid epidemic, there has been a rise in pregnant women diagnosed with opioid use disorder and cases of infants born with neonatal opioid withdrawal syndrome (NOWS). NOWS refers to signs and symptoms following cessation of prenatal opioid exposure that comprise neurological, gastrointestinal, and autonomic system dysfunction. A critical indicator of NOWS severity is excessive, high-pitched crying.

View Article and Find Full Text PDF

Minor prion substrains overcome transmission barriers.

mBio

November 2024

Department of Medical Microbiology and Immunology, School of Medicine, Creighton University, Omaha, Nebraska, USA.

Article Synopsis
  • Mammalian prion diseases are caused by a misfolded prion protein (PrP), and research indicates that these prions exist as a mix of dominant and minor strains, affecting their ability to cross species barriers.
  • * Recent findings show that minor prion strains derived from a hamster-adapted strain have a higher infection efficiency in rabbit kidney cells compared to the dominant strain, suggesting they play a significant role in species transmission.
  • * The study further reveals that minor strains outperformed the dominant strain in converting mouse PrP to infectious PrP, indicating greater diversity among these minor strains than previously thought, which has implications for understanding prion diseases and their zoonotic risks.
View Article and Find Full Text PDF

Aim: Compared with the C57BL/6N substrain, the C57BL/6J substrain is more susceptible to the angiotensin II (Ang II)-induced development of dissected abdominal aortic aneurysms (AAAs). The aim of this study was to elucidate whether the widely used C57BL/6N mouse substrain is as susceptible as the C57BL/6J mouse substrain to porcine pancreatic elastase (PPE) infusion-induced experimental nondissected AAA development.

Methods: Experimental nondissected AAAs were induced in C57BL/6J and C57BL/6N mice via transient aortic luminal infusion of PPE.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!