Impact of blood sampling technique on blood quality and animal welfare in haemophilic mice

血液取样 动物福利 福利 质量(理念) 采样(信号处理) 医学 环境卫生 生理学 生物 内科学 计算机科学 政治学 生态学 哲学 认识论 法学 滤波器(信号处理) 计算机视觉
作者
Heidi L. Holmberg,Maria Kristina Kiersgaard,Lars Friis Mikkelsen,Mikael Tranholm
出处
期刊:Laboratory Animals [SAGE Publishing]
卷期号:45 (2): 114-120 被引量:24
标识
DOI:10.1258/la.2010.010129
摘要

Blood collection in mice can be a challenge, in particular for samples used for coagulation analysis as initiation of coagulation during the procedures can influence the results. Blood collection from the retrobulbar venous plexus is commonly used but the method remains controversial. Several alternatives exist but not all are applicable to mice with a compromised coagulation system because of subsequently excessive bleeding. We therefore wanted to explore whether blood collection by puncture of the submandibular vein could replace blood collected from the retrobulbar venous plexus during pharmacokinetic and pharmacodynamic studies in mice lacking coagulation factor VIII (FVIII). The plasma concentrations of recombinant activated factor VII were independent of the blood collection method in a pharmacokinetic study. The same applied to the thromboelastographic profile of mice with normal coagulation in a pharmacodynamic study. However, excessive haemorrhages were observed in all FVIII knockout mice after a single puncture of the submandibular vein and 60% of the mice were euthanized 2–4 h after the blood collection. In contrast, no or only slight haemorrhage was observed in animals subjected to blood collection from the retrobulbar venous plexus. No signs of distress determined by blood glucose level or clinical abnormalities of the eye were observed after puncture of the retrobulbar venous plexus. In conclusion, blood collected by puncture of the submandibular vein and retrobulbar venous plexus has a quality which allows it to be used in coagulation assays. However, because of excessive bleedings, puncture of the submandibular vein is not recommended in mice lacking FVIII.
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