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1.
PLoS One ; 12(4): e0175839, 2017.
Article in English | MEDLINE | ID: mdl-28422994

ABSTRACT

The EU Directive 2010/63/EU changed the requirements regarding the use of laboratory animals and raised important issues related to assessing the severity of all procedures undertaken on laboratory animals. However, quantifiable parameters to assess severity are rare, and improved assessment strategies need to be developed. Hence, a Sheep Grimace Scale (SGS) was herein established by observing and interpreting sheep facial expressions as a consequence of pain and distress following unilateral tibia osteotomy. The animals were clinically investigated and scored five days before surgery and at 1, 3, 7, 10, 14 and 17 days afterwards. Additionally, cortisol levels in the saliva of the sheep were determined at the respective time points. For the SGS, video recording was performed, and pictures of the sheep were randomized and scored by blinded observers. Osteotomy in sheep resulted in an increased clinical severity score from days 1 to 17 post-surgery and elevated salivary cortisol levels one day post-surgery. An analysis of facial expressions revealed a significantly increased SGS on the day of surgery until day 3 post-surgery; this elevated level was sustained until day 17. Clinical severity and SGS scores correlated positively with a Pearson´s correlation coefficient of 0.47. Further investigations regarding the applicability of the SGS revealed a high inter-observer reliability with an intraclass correlation coefficient of 0.92 and an accuracy of 68.2%. In conclusion, the SGS represents a valuable approach for severity assessment that may help support and refine a widely used welfare assessment for sheep during experimental procedures, thereby meeting legislation requirements and minimizing the occurrence of unrecognized distress in animal experimentation.


Subject(s)
Osteotomy , Pain Measurement/methods , Pain/diagnosis , Tibia/surgery , Animal Welfare , Animals , Facial Expression , Female , Hydrocortisone/analysis , Hydrocortisone/metabolism , Observer Variation , Pain/physiopathology , Pain/surgery , Postoperative Period , Reproducibility of Results , Saliva/chemistry , Sheep, Domestic , Tibia/innervation , Video Recording
2.
Lab Anim ; 50(5): 400-3, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26678296

ABSTRACT

A disease affecting guinea pigs called 'guinea pig lameness' characterized by clinical signs of depression, lameness of limbs, flaccid paralysis, weight loss and death within a few weeks was first described by Römer in 1911. After a research group in our facility kept laboratory guinea pigs from two different origins together in one room, lameness was observed in two animals. Further investigations revealed a serological immune response against Theiler's murine encephalomyelitis virus (TMEV; GDVII strain) in these animals. Histopathology of the lumbar spinal cord of these animals showed mononuclear cell infiltration and necrotic neurons in the anterior horn. Therefore, all guinea pigs from this contaminated animal unit, from other units in our facility, as well as from different European institutions and breeding centres were screened for antibodies directed against GDVII. Our investigations showed that approximately 80% of all guinea pigs from the contaminated animal unit were seropositive for GDVII, whereas animals from other separate units were completely negative. In addition, 43% of tested sera from the different European institutions and breeding centres contained antibodies against GDVII. The present data confirm that an unknown viral infection causes an immune response in experimental guinea pigs leading to seroconversion against GDVII and that guinea pigs from a commercial breeder are the source of the infection.


Subject(s)
Cardiovirus Infections/epidemiology , Guinea Pigs , Lameness, Animal/epidemiology , Rodent Diseases/epidemiology , Theilovirus/isolation & purification , Animals , Antibodies, Viral/blood , Cardiovirus Infections/virology , Lameness, Animal/virology , Prevalence , Rodent Diseases/virology , Seroepidemiologic Studies
3.
J Comp Physiol B ; 177(1): 61-73, 2007 Jan.
Article in English | MEDLINE | ID: mdl-16868751

ABSTRACT

It was the aim of the present study to investigate chloride secretion across the proximal colon of Cftr (TgH(neoim)1Hgu) congenic mice. Stripped epithelia were incubated in Ussing chambers and the electrophysiological data were compared between cystic fibrosis (CF) animals and wild type (WT) animals. In comparison with the control animals, all Cftr (TgH(neoim)1Hgu) congenic mice had a distinctly reduced basal chloride secretion and a reduced chloride secretion after stimulation with carbachol and forskolin. When comparing chloride secretion across the proximal colon between WT animals, all mice showed a comparable pattern of response to carbachol and forskolin but quantitative differences, BALB/c exhibiting the highest and HsdOla:MF1 exhibiting the lowest increase in Cl current. Likewise, all CF animals showed the same reaction pattern to carbachol and forskolin, but there was no distinct difference that lasted for the whole measurement. To investigate interferences between Ca- and cyclic adenosine monophosphate-activated pathways of Cl secretion in CF animals, we studied epithelia from CF/3CF/1F1 animals with a mixed background. In these animals, the levels of the carbachol or forskolin-induced chloride currents did not depend on the prestimulation with the respective other secretagogue. 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid, which blocks calcium-activated chloride channels, reduced the current response to carbachol by about 23%. This result, obtained in BALB/c-Cftr (TgH(neoim)1Hgu) mice, indicates that alternative chloride channels might be present in the proximal colon of these mice. In contrast, there was no evidence for alternative chloride conductances in BALB/c WT animals, but we cannot exclude that in WT mice a higher chloride secretion via Cftr-channels may have masked an alternative chloride secretion.


Subject(s)
Chloride Channels/physiology , Chlorides/metabolism , Colon/metabolism , 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid/pharmacology , Amiloride/pharmacology , Animals , Barium/pharmacology , Biological Transport/physiology , Carbachol/pharmacology , Chloride Channels/antagonists & inhibitors , Chloride Channels/drug effects , Colforsin/pharmacology , Female , Male , Mice , Mice, Congenic/metabolism , Mice, Inbred BALB C , Mice, Inbred CFTR/metabolism , Nitrobenzoates/pharmacology , Potassium Channel Blockers/pharmacology , Sodium Channel Blockers/pharmacology , Tetraethylammonium/pharmacology
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