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BMC Physiology 2011
Metabolomic phenotyping of a cloned pig modelAbstract: The metabolic phenotype of cloned pigs (n = 5) was for the first time elucidated by nuclear magnetic resonance (NMR)-based metabolomic analysis of multiple bio-fluids including plasma, bile and urine. The metabolic phenotype of the cloned pigs was compared with normal outbred pigs (n = 6) by multivariate data analysis, which revealed differences in the metabolic phenotypes. Plasma lactate was higher for cloned vs control pigs, while multiple metabolites were altered in the bile. However a lower inter-individual variability for cloned pigs compared with control pigs could not be established.From the present study we conclude that cloned and normal outbred pigs are phenotypically different. However, it cannot be concluded that the use of cloned animals will reduce the inter-individual variation in intervention studies, though this is based on a limited number of animals.Use of animal models in research related to human health and nutrition is common practice for example in dietary intervention studies. There are several reasons for using animal models. Firstly, the access to several bio-fluids and organs is possible. Secondly, it is easier to control animals than humans and to secure compliance to the experimental diet. This should lead to smaller inter-individual differences which are necessary for showing effects of the compound/diet under investigation. For this reason we hypothesize that a cloned animal model would be beneficial for intervention studies, as they are expected to provide a more controlled and repeatable experimental system that requires fewer animals compared with outbred lines.In particular, the pig has become a widely used model, since pigs from a nutritional aspect are comparable to humans [1,2], and their lipoprotein profile and metabolism are similar to that of humans [3-6]. Recently, a cloned pig model was used as a model for studying atherosclerosis [7]. However, the use of cloned animals in nutrition studies is still in its opening stage, an
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