ISSN:
1433-2981
Keywords:
Clinical chemistry
;
Dog
;
Fasting
;
Haematology
;
Rat
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstract Many regulatory toxicity guidelines and the recommendation of AACC-DACC/ASVCP joint task force of the USA on clinical pathology testing require overnight fasting for rats and non-rodents before blood sampling. However, the reason why animals must be fasted before blood sampling is unclear in toxicology studies. Fasting, one of many preanalytical conditions, can lead to false low or high values, which in turn may lead to misinterpretation of test compound effects in toxicological studies. This paper reviews the literature with respect to fasting, and reports on our own studies, in the hope of increasing the awareness among investigators of these problems. Haematocrit values and plasma chemistry values in blood obtained from rats and dogs following fasting were compared with unfasted animals. In male F344 rats, after 16 h fasting, body weight decreased. Increases in aspartate aminotransferase (AST)/glutamic oxaloacetic transaminase (GOT) and decreases of plasma alkaline phosphatase (ALP), total cholesterol (CHO), triglycerides (TG), phospholipids (PL), urea nitrogen (UN) and calcium were observed. Haematocrit, plasma alanine aminotransferase (ALT)/glutamic pyruvic transaminase (GPT), total proteins (TP), glucose, and inorganic phosphorus (IP) were unchanged. In male beagle dogs after 16 h fasting, TG, PL, UN, calcium and IP were decreased. Haematocrit, ALP, TP, albumin, glucose, CHO, creatinine, AST/GOT, ALT/GPT, LDH and CPK were not changed. Our own studies show that in order to avoid excessive stress to test animals, the fasting period should be decided case by case, and not made uniform in toxicology studies. It would be useful if regulatory guidelines made some mention of both the effect of feeding, and of stress caused by fasting.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00798356
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